Targeting NLRP3 Inflammasome: Structure, Function, and Inhibitors
- Авторлар: Lou S.1, Wu M.2, Cui S.1
-
Мекемелер:
- Institute of Drug Discovery and Design, College of Pharmaceutical Sciences, Zhejiang University
- Department of Pharmacy, The Fourth Affiliated Hospital, Zhejiang University School of Medicine
- Шығарылым: Том 31, № 15 (2024)
- Беттер: 2021-2051
- Бөлім: Anti-Infectives and Infectious Diseases
- URL: https://rjpbr.com/0929-8673/article/view/644396
- DOI: https://doi.org/10.2174/0109298673289984231127062528
- ID: 644396
Дәйексөз келтіру
Толық мәтін
Аннотация
Inflammasomes are multimeric protein complexes that can detect various physiological stimuli and danger signals. As a result, they perform a crucial function in the innate immune response. The NLRP3 inflammasome, as a vital constituent of the inflammasome family, is significant in defending against pathogen invasion and preserving cellhomeostasis. NLRP3 inflammasome dysregulation is connected to various pathological conditions, including inflammatory diseases, cancer, and cardiovascular and neurodegenerative diseases. This profile makes NLRP3 an applicable target for treating related diseases, and therefore, there are rising NLRP3 inhibitors disclosed for therapy. Herein, we summarized the updated advances in the structure, function, and inhibitors of NLRP3 inflammasome. Moreover, we aimed to provide an overview of the existing products and future directions for drug research and development.
Негізгі сөздер
Авторлар туралы
Shengying Lou
Institute of Drug Discovery and Design, College of Pharmaceutical Sciences, Zhejiang University
Email: info@benthamscience.net
Miaolian Wu
Department of Pharmacy, The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Хат алмасуға жауапты Автор.
Email: info@benthamscience.net
Sunliang Cui
Institute of Drug Discovery and Design, College of Pharmaceutical Sciences, Zhejiang University
Хат алмасуға жауапты Автор.
Email: info@benthamscience.net
Әдебиет тізімі
- Martinon, F.; Burns, K.; Tschopp, J. The Inflammasome. Mol. Cell, 2002, 10(2), 417-426. doi: 10.1016/S1097-2765(02)00599-3 PMID: 12191486
- Zheng, D.; Liwinski, T.; Elinav, E. Inflammasome activation and regulation: Toward a better understanding of complex mechanisms. Cell Discov., 2020, 6(1), 36. doi: 10.1038/s41421-020-0167-x PMID: 32550001
- Singh, P.; Kumar, N.; Singh, M.; Kaur, M.; Singh, G.; Narang, A.; Kanwal, A.; Sharma, K.; Singh, B.; Napoli, M.D.; Mastana, S. Neutrophil extracellular traps and NLRP3 inflammasome: A disturbing duo in atherosclerosis, inflammation and atherothrombosis. Vaccines, 2023, 11(2), 261. doi: 10.3390/vaccines11020261 PMID: 36851139
- Sharma, D.; Kanneganti, T.D. The cell biology of inflammasomes: Mechanisms of inflammasome activation and regulation. J. Cell Biol., 2016, 213(6), 617-629. doi: 10.1083/jcb.201602089 PMID: 27325789
- Christgen, S.; Place, D.E.; Kanneganti, T.D. Toward targeting inflammasomes: Insights into their regulation and activation. Cell Res., 2020, 30(4), 315-327. doi: 10.1038/s41422-020-0295-8 PMID: 32152420
- Xu, J.; Núñez, G. The NLRP3 inflammasome: Activation and regulation. Trends Biochem. Sci., 2023, 48(4), 331-344. doi: 10.1016/j.tibs.2022.10.002 PMID: 36336552
- Ohto, U.; Kamitsukasa, Y.; Ishida, H.; Zhang, Z.; Murakami, K.; Hirama, C.; Maekawa, S.; Shimizu, T. Structural basis for the oligomerization-mediated regulation of NLRP3 inflammasome activation. Proc. Natl. Acad. Sci., 2022, 119(11), e2121353119. doi: 10.1073/pnas.2121353119 PMID: 35254907
- Tapia-Abellán, A.; Angosto-Bazarra, D.; Alarcón-Vila, C.; Baños, M. C; Hafner-Bratkovič, I.; Oliva, B.; Pelegrín, P. Sensing low intracellular potassium by NLRP3 results in a stable open structure that promotes inflammasome activation. Sci. Adv., 2021, 7, eabf44. doi: 10.1126/sciadv.abf4468
- Dekker, C.; Mattes, H.; Wright, M.; Boettcher, A.; Hinniger, A.; Hughes, N.; Kapps-Fouthier, S.; Eder, J.; Erbel, P.; Stiefl, N.; Mackay, A.; Farady, C.J. Crystal structure of NLRP3 NACHT domain with an inhibitor defines mechanism of inflammasome inhibition. J. Mol. Biol., 2021, 433(24), 167309. doi: 10.1016/j.jmb.2021.167309 PMID: 34687713
- Sharif, H.; Wang, L.; Wang, W.L.; Magupalli, V.G.; Andreeva, L.; Qiao, Q.; Hauenstein, A.V.; Wu, Z.; Núñez, G.; Mao, Y.; Wu, H. Structural mechanism for NEK7-licensed activation of NLRP3 inflammasome. Nature, 2019, 570(7761), 338-343. doi: 10.1038/s41586-019-1295-z PMID: 31189953
- Andreeva, L.; David, L.; Rawson, S.; Shen, C.; Pasricha, T.; Pelegrin, P.; Wu, H. NLRP3 cages revealed by full-length mouse NLRP3 structure control pathway activation. Cell, 2021, 184(26), 6299-6312.e22. doi: 10.1016/j.cell.2021.11.011 PMID: 34861190
- Hafner-Bratkovič, I. NLRP3 is its own gatekeeper: A group hug of NLRP3 monomers controls inflammation. Trends Biochem. Sci., 2022, 47(8), 635-637. doi: 10.1016/j.tibs.2022.03.014 PMID: 35382945
- Hochheiser, I.V.; Pilsl, M.; Hagelueken, G.; Moecking, J.; Marleaux, M.; Brinkschulte, R.; Latz, E.; Engel, C.; Geyer, M. Structure of the NLRP3 decamer bound to the cytokine release inhibitor CRID3. Nature, 2022, 604(7904), 184-189. doi: 10.1038/s41586-022-04467-w PMID: 35114687
- Xiao, L.; Magupalli, V.G.; Wu, H. Cryo-EM structures of the active NLRP3 inflammasome disc. Nature, 2023, 613(7944), 595-600. doi: 10.1038/s41586-022-05570-8 PMID: 36442502
- Swanson, K.V.; Deng, M.; Ting, J.P.Y. The NLRP3 inflammasome: molecular activation and regulation to therapeutics. Nat. Rev. Immunol., 2019, 19(8), 477-489. doi: 10.1038/s41577-019-0165-0 PMID: 31036962
- Li, Y.; Fu, T.M.; Lu, A.; Witt, K.; Ruan, J.; Shen, C.; Wu, H. Cryo-EM structures of ASC and NLRC4 CARD filaments reveal a unified mechanism of nucleation and activation of caspase-1. Proc. Natl. Acad. Sci., 2018, 115(43), 10845-10852. doi: 10.1073/pnas.1810524115 PMID: 30279182
- Vong, C.T.; Tseng, H.H.L.; Yao, P.; Yu, H.; Wang, S.; Zhong, Z.; Wang, Y. Specific NLRP3 inflammasome inhibitors: Promising therapeutic agents for inflammatory diseases. Drug Discov. Today, 2021, 26(6), 1394-1408. doi: 10.1016/j.drudis.2021.02.018 PMID: 33636340
- Fu, J.; Wu, H. Structural mechanisms of NLRP3 inflammasome assembly and activation. Annu. Rev. Immunol., 2023, 41(1), 301-316. doi: 10.1146/annurev-immunol-081022-021207 PMID: 36750315
- Lamkanfi, M.; Dixit, V.M. A new lead to NLRP3 inhibition. J. Exp. Med., 2017, 214(11), 3147-3149. doi: 10.1084/jem.20171848 PMID: 29061692
- Mangan, M.S.J.; Olhava, E.J.; Roush, W.R.; Seidel, H.M.; Glick, G.D.; Latz, E. Targeting the NLRP3 inflammasome in inflammatory diseases. Nat. Rev. Drug Discov., 2018, 17(8), 588-606. doi: 10.1038/nrd.2018.97 PMID: 30026524
- Accogli, T.; Hibos, C.; Vegran, F. Canonical and non-canonical functions of NLRP3. J. Adv. Res., 2023, 53, 137-151. doi: 10.1016/j.jare.2023.01.001 PMID: 36610670
- Yang, Y.; Wang, H.; Kouadir, M.; Song, H.; Shi, F. Recent advances in the mechanisms of NLRP3 inflammasome activation and its inhibitors. Cell Death Dis., 2019, 10(2), 128. doi: 10.1038/s41419-019-1413-8 PMID: 30755589
- Paik, S.; Kim, J.K.; Silwal, P.; Sasakawa, C.; Jo, E.K. An update on the regulatory mechanisms of NLRP3 inflammasome activation. Cell. Mol. Immunol., 2021, 18(5), 1141-1160. doi: 10.1038/s41423-021-00670-3 PMID: 33850310
- Song, N.; Liu, Z.S.; Xue, W.; Bai, Z.F.; Wang, Q.Y.; Dai, J.; Liu, X.; Huang, Y.J.; Cai, H.; Zhan, X.Y.; Han, Q.Y.; Wang, H.; Chen, Y.; Li, H.Y.; Li, A.L.; Zhang, X.M.; Zhou, T.; Li, T. NLRP3 phosphorylation is an essential priming event for inflammasome activation. Mol. Cell, 2017, 68(1), 185-197.e6. doi: 10.1016/j.molcel.2017.08.017 PMID: 28943315
- Xu, T.; Yu, W.; Fang, H.; Wang, Z.; Chi, Z.; Guo, X.; Jiang, D.; Zhang, K.; Chen, S.; Li, M.; Guo, Y.; Zhang, J.; Yang, D.; Yu, Q.; Wang, D.; Zhang, X. Ubiquitination of NLRP3 by gp78/Insig-1 restrains NLRP3 inflammasome activation. Cell Death Differ., 2022, 29(8), 1582-1595. doi: 10.1038/s41418-022-00947-8 PMID: 35110683
- Ge, Q.; Chen, X.; Zhao, Y.; Mu, H.; Zhang, J. Modulatory mechanisms of NLRP3: Potential roles in inflammasome activation. Life Sci., 2021, 267, 118918. doi: 10.1016/j.lfs.2020.118918 PMID: 33352170
- Gong, T.; Yang, Y.; Jin, T.; Jiang, W.; Zhou, R. Orchestration of NLRP3 inflammasome activation by ion fluxes. Trends Immunol., 2018, 39(5), 393-406. doi: 10.1016/j.it.2018.01.009 PMID: 29452983
- Chen, M.; Ye, X.; He, X.; Ouyang, D. The signaling pathways regulating NLRP3 inflammasome activation. Inflammation, 2021, 44(4), 1229-1245. doi: 10.1007/s10753-021-01439-6 PMID: 34009550
- Wang, L.; Sharif, H.; Vora, S.M.; Zheng, Y.; Wu, H. Structures and functions of the inflammasome engine. J. Allergy Clin. Immunol., 2021, 147(6), 2021-2029. doi: 10.1016/j.jaci.2021.04.018 PMID: 34092352
- Dowling, J.K.; ONeill, L.A.J. Biochemical regulation of the inflammasome. Crit. Rev. Biochem. Mol. Biol., 2012, 47(5), 424-443. doi: 10.3109/10409238.2012.694844 PMID: 22681257
- Haneklaus, M.; ONeill, L.A.J.; Coll, R.C. Modulatory mechanisms controlling the NLRP3 inflammasome in inflammation: Recent developments. Curr. Opin. Immunol., 2013, 25(1), 40-45. doi: 10.1016/j.coi.2012.12.004 PMID: 23305783
- Kayagaki, N.; Warming, S.; Lamkanfi, M.; Walle, L.V.; Louie, S.; Dong, J.; Newton, K.; Qu, Y.; Liu, J.; Heldens, S.; Zhang, J.; Lee, W.P.; Roose-Girma, M.; Dixit, V.M. Non-canonical inflammasome activation targets caspase-11. Nature, 2011, 479(7371), 117-121. doi: 10.1038/nature10558 PMID: 22002608
- Shi, J.; Zhao, Y.; Wang, Y.; Gao, W.; Ding, J.; Li, P.; Hu, L.; Shao, F. Inflammatory caspases are innate immune receptors for intracellular LPS. Nature, 2014, 514(7521), 187-192. doi: 10.1038/nature13683 PMID: 25119034
- Moretti, J.; Jia, B.; Hutchins, Z.; Roy, S.; Yip, H.; Wu, J.; Shan, M.; Jaffrey, S.R.; Coers, J.; Blander, J.M. Caspase-11 interaction with NLRP3 potentiates the noncanonical activation of the NLRP3 inflammasome. Nat. Immunol., 2022, 23(5), 705-717. doi: 10.1038/s41590-022-01192-4 PMID: 35487985
- Yang, Z.H.; Han, J. Dual ligand engagement for noncanonical inflammasome activation. Nat. Immunol., 2022, 23(5), 651-653. doi: 10.1038/s41590-022-01188-0 PMID: 35487984
- Gaidt, M.M.; Ebert, T.S.; Chauhan, D.; Schmidt, T.; Schmid-Burgk, J.L.; Rapino, F.; Robertson, A.A.B.; Cooper, M.A.; Graf, T.; Hornung, V. Human monocytes engage an alternative inflammasome pathway. Immunity, 2016, 44(4), 833-846. doi: 10.1016/j.immuni.2016.01.012 PMID: 27037191
- Huang, Y.; Xu, W.; Zhou, R. NLRP3 inflammasome activation and cell death. Cell. Mol. Immunol., 2021, 18(9), 2114-2127. doi: 10.1038/s41423-021-00740-6 PMID: 34321623
- Li, Y.; Huang, H.; Liu, B.; Zhang, Y.; Pan, X.; Yu, X.Y.; Shen, Z.; Song, Y.H. Inflammasomes as therapeutic targets in human diseases. Signal Transduct. Target. Ther., 2021, 6(1), 247. doi: 10.1038/s41392-021-00650-z PMID: 34210954
- Moltrasio, C.; Romagnuolo, M.; Marzano, A.V. NLRP3 inflammasome and NLRP3-related autoinflammatory diseases: From cryopyrin function to targeted therapies. Front. Immunol., 2022, 13, 1007705. doi: 10.3389/fimmu.2022.1007705 PMID: 36275641
- de Torre-Minguela, C.; Mesa del Castillo, P.; Pelegrín, P. The NLRP3 and pyrin inflammasomes: Implications in the pathophysiology of autoinflammatory diseases. Front. Immunol., 2017, 8, 43. doi: 10.3389/fimmu.2017.00043 PMID: 28191008
- de Jesus, A.A.; Canna, S.W.; Liu, Y.; Goldbach-Mansky, R. Molecular mechanisms in genetically defined autoinflammatory diseases: Disorders of amplified danger signaling. Annu. Rev. Immunol., 2015, 33(1), 823-874. doi: 10.1146/annurev-immunol-032414-112227 PMID: 25706096
- Booshehri, L.M.; Hoffman, H.M. CAPS and NLRP3. J. Clin. Immunol., 2019, 39(3), 277-286. doi: 10.1007/s10875-019-00638-z PMID: 31077002
- Cuisset, L.; Jeru, I.; Dumont, B.; Fabre, A.; Cochet, E.; Le Bozec, J.; Delpech, M.; Amselem, S.; Touitou, I. Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: Epidemiological study and lessons from eight years of genetic analysis in France. Ann. Rheum. Dis., 2011, 70(3), 495-499. doi: 10.1136/ard.2010.138420 PMID: 21109514
- Theodoropoulou, K.; Spel, L.; Zaffalon, L.; Delacrétaz, M.; Hofer, M.; Martinon, F. NLRP3 leucine-rich repeats control induced and spontaneous inflammasome activation in cryopyrin-associated periodic syndrome. J. Allergy Clin. Immunol., 2023, 151(1), 222-232.e9. doi: 10.1016/j.jaci.2022.08.019 PMID: 36075321
- Guan, Q. A comprehensive review and update on the pathogenesis of inflammatory bowel disease. J. Immunol. Res., 2019, 2019, 1-16. doi: 10.1155/2019/7247238 PMID: 31886308
- Bauer, C.; Duewell, P.; Mayer, C.; Lehr, H.A.; Fitzgerald, K.A.; Dauer, M.; Tschopp, J.; Endres, S.; Latz, E.; Schnurr, M. Colitis induced in mice with dextran sulfate sodium (DSS) is mediated by the NLRP3 inflammasome. Gut, 2010, 59(9), 1192-1199. doi: 10.1136/gut.2009.197822 PMID: 20442201
- Liu, L.; Dong, Y.; Ye, M.; Jin, S.; Yang, J.; Joosse, M.E.; Sun, Y.; Zhang, J.; Lazarev, M.; Brant, S.R.; Safar, B.; Marohn, M.; Mezey, E.; Li, X. The pathogenic role of NLRP3 inflammasome activation in inflammatory bowel diseases of both mice and humans. J. Crohns Colitis, 2017, 11(6), 737-750. PMID: 27993998
- Wang, S.L.; Zhang, M.M.; Zhou, H.; Su, G.Q.; Ding, Y.; Xu, G.H.; Wang, X.; Li, C.F.; Huang, W.F.; Yi, L.T. Inhibition of NLRP3 attenuates sodium dextran sulfate-induced inflammatory bowel disease through gut microbiota regulation. Biomed. J., 2023, 46(5), 100580. doi: 10.1016/j.bj.2023.01.004 PMID: 36758943
- Chen, Q.L.; Yin, H.R.; He, Q.Y.; Wang, Y. Targeting the NLRP3 inflammasome as new therapeutic avenue for inflammatory bowel disease. Biomed. Pharmacother., 2021, 138, 111442. doi: 10.1016/j.biopha.2021.111442 PMID: 33667791
- Zaki, M.H.; Boyd, K.L.; Vogel, P.; Kastan, M.B.; Lamkanfi, M.; Kanneganti, T.D. The NLRP3 inflammasome protects against loss of epithelial integrity and mortality during experimental colitis. Immunity, 2010, 32(3), 379-391. doi: 10.1016/j.immuni.2010.03.003 PMID: 20303296
- Song, Y.; Zhao, Y.; Ma, Y.; Wang, Z.; Rong, L.; Wang, B.; Zhang, N. Biological functions of NLRP3 inflammasome: A therapeutic target in inflammatory bowel disease. Cytokine Growth Factor Rev., 2021, 60, 61-75. doi: 10.1016/j.cytogfr.2021.03.003 PMID: 33773897
- Zhen, Y.; Zhang, H. NLRP3 inflammasome and inflammatory bowel disease. Front. Immunol., 2019, 10, 276. doi: 10.3389/fimmu.2019.00276 PMID: 30873162
- Toldo, S.; Mezzaroma, E.; Buckley, L.F.; Potere, N.; Di Nisio, M.; Biondi-Zoccai, G.; Van Tassell, B.W.; Abbate, A. Targeting the NLRP3 inflammasome in cardiovascular diseases. Pharmacol. Ther., 2022, 236, 108053. doi: 10.1016/j.pharmthera.2021.108053 PMID: 34906598
- Grebe, A.; Hoss, F.; Latz, E. NLRP3 inflammasome and the IL-1 pathway in atherosclerosis. Circ. Res., 2018, 122(12), 1722-1740. doi: 10.1161/CIRCRESAHA.118.311362 PMID: 29880500
- Baldrighi, M.; Mallat, Z.; Li, X. NLRP3 inflammasome pathways in atherosclerosis. Atherosclerosis, 2017, 267, 127-138. doi: 10.1016/j.atherosclerosis.2017.10.027 PMID: 29126031
- Poznyak, A.V.; Melnichenko, A.A.; Wetzker, R.; Gerasimova, E.V.; Orekhov, A.N. NLPR3 inflammasomes and their significance for atherosclerosis. Biomedicines, 2020, 8(7), 205. doi: 10.3390/biomedicines8070205 PMID: 32664349
- Jiang, C.; Xie, S.; Yang, G.; Wang, N. Spotlight on NLRP3 inflammasome: Role in pathogenesis and therapies of atherosclerosis. J. Inflamm. Res., 2021, 14, 7143-7172. doi: 10.2147/JIR.S344730 PMID: 34992411
- Hoseini, Z.; Sepahvand, F.; Rashidi, B.; Sahebkar, A.; Masoudifar, A.; Mirzaei, H. NLRP3 inflammasome: Its regulation and involvement in atherosclerosis. J. Cell. Physiol., 2018, 233(3), 2116-2132. doi: 10.1002/jcp.25930 PMID: 28345767
- Duewell, P.; Kono, H.; Rayner, K.J.; Sirois, C.M.; Vladimer, G.; Bauernfeind, F.G.; Abela, G.S.; Franchi, L.; Nuñez, G.; Schnurr, M.; Espevik, T.; Lien, E.; Fitzgerald, K.A.; Rock, K.L.; Moore, K.J.; Wright, S.D.; Hornung, V.; Latz, E. NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals. Nature, 2010, 464(7293), 1357-1361. doi: 10.1038/nature08938 PMID: 20428172
- Zheng, F.; Xing, S.; Gong, Z.; Mu, W.; Xing, Q. Cancer statistics. Cancer J. Clin., 2014, 73, 17-48.
- Siegel, R.L.; Miller, K.D.; Wagle, N.S.; Jemal, A. Cancer statistics, 2023. CA Cancer J. Clin., 2023, 73(1), 17-48. doi: 10.3322/caac.21763 PMID: 36633525
- Siegel, R.; Ma, J.; Zou, Z.; Jemal, A. Cancer statistics, 2014. CA Cancer J. Clin., 2014, 64(1), 9-29. doi: 10.3322/caac.21208 PMID: 24399786
- Moossavi, M.; Parsamanesh, N.; Bahrami, A.; Atkin, S.L.; Sahebkar, A. Role of the NLRP3 inflammasome in cancer. Mol. Cancer, 2018, 17(1), 158. doi: 10.1186/s12943-018-0900-3 PMID: 30447690
- Dostert, C.; Pétrilli, V.; Van Bruggen, R.; Steele, C.; Mossman, B.T.; Tschopp, J. Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica. Science, 2008, 320(5876), 674-677. doi: 10.1126/science.1156995 PMID: 18403674
- Cox, L.A., Jr Dose-response modeling of NLRP3 inflammasome-mediated diseases: Asbestos, lung cancer, and malignant mesothelioma as examples. Crit. Rev. Toxicol., 2019, 49(7), 614-635. doi: 10.1080/10408444.2019.1692779 PMID: 31905042
- Wang, Y.; Kong, H.; Zeng, X.; Liu, W.; Wang, Z.; Yan, X.; Wang, H.; Xie, W. Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells. Oncol. Rep., 2016, 35(4), 2053-2064. doi: 10.3892/or.2016.4569 PMID: 26782741
- Faria, S.S.; Costantini, S.; de Lima, V.C.C.; de Andrade, V.P.; Rialland, M.; Cedric, R.; Budillon, A.; Magalhães, K.G. NLRP3 inflammasome-mediated cytokine production and pyroptosis cell death in breast cancer. J. Biomed. Sci., 2021, 28(1), 26. doi: 10.1186/s12929-021-00724-8 PMID: 33840390
- Ershaid, N.; Sharon, Y.; Doron, H.; Raz, Y.; Shani, O.; Cohen, N.; Monteran, L.; Leider-Trejo, L.; Ben-Shmuel, A.; Yassin, M.; Gerlic, M.; Ben-Baruch, A.; Pasmanik-Chor, M.; Apte, R.; Erez, N. NLRP3 inflammasome in fibroblasts links tissue damage with inflammation in breast cancer progression and metastasis. Nat. Commun., 2019, 10(1), 4375. doi: 10.1038/s41467-019-12370-8 PMID: 31558756
- Wang, Y.; Zhang, H.; Xu, Y.; Peng, T.; Meng, X.; Zou, F. NLRP3 induces the autocrine secretion of IL-1β to promote epithelialmesenchymal transition and metastasis in breast cancer. Biochem. Biophys. Res. Commun., 2021, 560, 72-79. doi: 10.1016/j.bbrc.2021.04.122 PMID: 33975248
- Guo, B.; Fu, S.; Zhang, J.; Liu, B.; Li, Z. Targeting inflammasome/IL-1 pathways for cancer immunotherapy. Sci. Rep., 2016, 6(1), 36107. doi: 10.1038/srep36107 PMID: 27786298
- Missiroli, S.; Perrone, M.; Boncompagni, C.; Borghi, C.; Campagnaro, A.; Marchetti, F.; Anania, G.; Greco, P.; Fiorica, F.; Pinton, P.; Giorgi, C. Targeting the NLRP3 inflammasome as a new therapeutic option for overcoming cancer. Cancers, 2021, 13(10), 2297. doi: 10.3390/cancers13102297 PMID: 34064909
- Peek, R.M., Jr Orchestration of aberrant epithelial signaling by Helicobacter pylori CagA. Sci. STKE, 2005, 2005(277), pe14. doi: 10.1126/stke.2772005pe14 PMID: 15798102
- Lamb, A.; Chen, L.F. Role of the Helicobacter pylori -induced inflammatory response in the development of gastric cancer. J. Cell. Biochem., 2013, 114(3), 491-497. doi: 10.1002/jcb.24389 PMID: 22961880
- Semper, R.P.; Mejías-Luque, R.; Groß, C.; Anderl, F.; Müller, A.; Vieth, M.; Busch, D.H.; Prazeres da Costa, C.; Ruland, J.; Groß, O.; Gerhard, M. Helicobacter pylori-induced IL-1β secretion in innate immune cells is regulated by the NLRP3 inflammasome and requires the cag pathogenicity island. J. Immunol., 2014, 193(7), 3566-3576. doi: 10.4049/jimmunol.1400362 PMID: 25172489
- Deans, D A C.; Wigmore, S.J.; Gilmour, H.; Paterson-Brown, S.; Ross, J.A.; Fearon, K.C.H. Elevated tumour interleukin-1β is associated with systemic inflammation: a marker of reduced survival in gastro-oesophageal cancer. Br. J. Cancer, 2006, 95(11), 1568-1575. doi: 10.1038/sj.bjc.6603446 PMID: 17088911
- Bagheri, V.; Memar, B.; Momtazi, A.A.; Sahebkar, A.; Gholamin, M.; Abbaszadegan, M.R. Cytokine networks and their association with Helicobacter pylori infection in gastric carcinoma. J. Cell. Physiol., 2018, 233(4), 2791-2803. doi: 10.1002/jcp.25822 PMID: 28121015
- Li, S.; Liang, X.; Ma, L.; Shen, L.; Li, T.; Zheng, L.; Sun, A.; Shang, W.; Chen, C.; Zhao, W.; Jia, J. MiR-22 sustains NLRP3 expression and attenuates H. pylori-induced gastric carcinogenesis. Oncogene, 2018, 37(7), 884-896. doi: 10.1038/onc.2017.381 PMID: 29059152
- Karki, R.; Kanneganti, T.D. Diverging inflammasome signals in tumorigenesis and potential targeting. Nat. Rev. Cancer, 2019, 19(4), 197-214. doi: 10.1038/s41568-019-0123-y PMID: 30842595
- Hamarsheh, S.; Zeiser, R. NLRP3 inflammasome activation in cancer: A double-edged sword. Front. Immunol., 2020, 11, 1444. doi: 10.3389/fimmu.2020.01444 PMID: 32733479
- Zaki, M.H.; Vogel, P.; Body-Malapel, M.; Lamkanfi, M.; Kanneganti, T.D. IL-18 production downstream of the Nlrp3 inflammasome confers protection against colorectal tumor formation. J. Immunol., 2010, 185(8), 4912-4920. doi: 10.4049/jimmunol.1002046 PMID: 20855874
- Sharma, B.R.; Kanneganti, T.D. NLRP3 inflammasome in cancer and metabolic diseases. Nat. Immunol., 2021, 22(5), 550-559. doi: 10.1038/s41590-021-00886-5 PMID: 33707781
- McCarron, R.M.; Shapiro, B.; Rawles, J. Luo, J. Depression. Ann. Intern. Med., 2021, 174(5), ITC65-ITC80. doi: 10.7326/AITC202105180 PMID: 33971098
- Miller, A.H.; Maletic, V.; Raison, C.L. Inflammation and its discontents: The role of cytokines in the pathophysiology of major depression. Biol. Psychiatry, 2009, 65(9), 732-741. doi: 10.1016/j.biopsych.2008.11.029 PMID: 19150053
- Iwata, M.; Ota, K.T.; Duman, R.S. The inflammasome: Pathways linking psychological stress, depression, and systemic illnesses. Brain Behav. Immun., 2013, 31, 105-114. doi: 10.1016/j.bbi.2012.12.008 PMID: 23261775
- Zhang, Y.; Liu, L.; Peng, Y.L.; Liu, Y.Z.; Wu, T.Y.; Shen, X.L.; Zhou, J.R.; Sun, D.Y.; Huang, A.J.; Wang, X.; Wang, Y.X.; Jiang, C.L. Involvement of inflammasome activation in lipopolysaccharide-induced mice depressive-like behaviors. CNS Neurosci. Ther., 2014, 20(2), 119-124. doi: 10.1111/cns.12170 PMID: 24279434
- Alcocer-Gómez, E.; Ulecia-Morón, C.; Marín-Aguilar, F.; Rybkina, T.; Casas-Barquero, N.; Ruiz-Cabello, J.; Ryffel, B.; Apetoh, L.; Ghiringhelli, F.; Bullón, P.; Sánchez-Alcazar, J.A.; Carrión, A.M.; Cordero, M.D. Stress-induced depressive behaviors require a functional NLRP3 inflammasome. Mol. Neurobiol., 2016, 53(7), 4874-4882. doi: 10.1007/s12035-015-9408-7 PMID: 26362308
- Kaufmann, F.N.; Costa, A.P.; Ghisleni, G.; Diaz, A.P.; Rodrigues, A.L.S.; Peluffo, H.; Kaster, M.P. NLRP3 inflammasome-driven pathways in depression: Clinical and preclinical findings. Brain Behav. Immun., 2017, 64, 367-383. doi: 10.1016/j.bbi.2017.03.002 PMID: 28263786
- Liang, T.; Zhang, Y.; Wu, S.; Chen, Q.; Wang, L. The role of NLRP3 inflammasome in Alzheimers disease and potential therapeutic targets. Front. Pharmacol., 2022, 13, 845185. doi: 10.3389/fphar.2022.845185 PMID: 35250595
- Heneka, M.T.; Kummer, M.P.; Stutz, A.; Delekate, A.; Schwartz, S.; Vieira-Saecker, A.; Griep, A.; Axt, D.; Remus, A.; Tzeng, T.C.; Gelpi, E.; Halle, A.; Korte, M.; Latz, E.; Golenbock, D.T. NLRP3 is activated in Alzheimers disease and contributes to pathology in APP/PS1 mice. Nature, 2013, 493(7434), 674-678. doi: 10.1038/nature11729 PMID: 23254930
- Saresella, M.; La Rosa, F.; Piancone, F.; Zoppis, M.; Marventano, I.; Calabrese, E.; Rainone, V.; Nemni, R.; Mancuso, R.; Clerici, M. The NLRP3 and NLRP1 inflammasomes are activated in Alzheimers disease. Mol. Neurodegener., 2016, 11(1), 23. doi: 10.1186/s13024-016-0088-1 PMID: 26939933
- Ahmed, M.E.; Iyer, S.; Thangavel, R.; Kempuraj, D.; Selvakumar, G.P.; Raikwar, S.P.; Zaheer, S.; Zaheer, A. Co-Localization of glia maturation factor with NLRP3 inflammasome and autophagosome markers in human Alzheimers disease brain. J. Alzheimers Dis., 2017, 60(3), 1143-1160. doi: 10.3233/JAD-170634 PMID: 28984607
- Milner, M.T.; Maddugoda, M.; Götz, J.; Burgener, S.S.; Schroder, K. The NLRP3 inflammasome triggers sterile neuroinflammation and Alzheimers disease. Curr. Opin. Immunol., 2021, 68, 116-124. doi: 10.1016/j.coi.2020.10.011 PMID: 33181351
- Feng, Y.S.; Tan, Z.X.; Wu, L.Y.; Dong, F.; Zhang, F. The involvement of NLRP3 inflammasome in the treatment of Alzheimers disease. Ageing Res. Rev., 2020, 64, 101192. doi: 10.1016/j.arr.2020.101192 PMID: 33059089
- Ding, S.; Xu, S.; Ma, Y.; Liu, G.; Jang, H.; Fang, J. Modulatory mechanisms of the NLRP3 inflammasomes in diabetes. Biomolecules, 2019, 9(12), 850. doi: 10.3390/biom9120850 PMID: 31835423
- Esser, N.; Lhomme, L.; De Roover, A.; Kohnen, L.; Scheen, A.J.; Moutschen, M.; Piette, J.; Legrand-Poels, S.; Paquot, N. Obesity phenotype is related to NLRP3 inflammasome activity and immunological profile of visceral adipose tissue. Diabetologia, 2013, 56(11), 2487-2497. doi: 10.1007/s00125-013-3023-9
- Gora, I.M.; Ciechanowska, A.; Ladyzynski, P. NLRP3 inflammasome at the interface of inflammation, endothelial dysfunction, and type 2 diabetes. Cells, 2021, 10(2), 314. doi: 10.3390/cells10020314 PMID: 33546399
- Lamkanfi, M.; Mueller, J.L.; Vitari, A.C.; Misaghi, S.; Fedorova, A.; Deshayes, K.; Lee, W.P.; Hoffman, H.M.; Dixit, V.M. Glyburide inhibits the Cryopyrin/Nalp3 inflammasome. J. Cell Biol., 2009, 187(1), 61-70. doi: 10.1083/jcb.200903124 PMID: 19805629
- Carvalho, A.M.; Novais, F.O.; Paixão, C.S.; de Oliveira, C.I.; Machado, P.R.L.; Carvalho, L.P.; Scott, P.; Carvalho, E.M. Glyburide, a NLRP3 inhibitor, decreases inflammatory response and is a candidate to reduce pathology in leishmania Braziliensis infection. J. Invest. Dermatol., 2020, 140(1), 246-249.e2. doi: 10.1016/j.jid.2019.05.025 PMID: 31252034
- Zhang, G.; Lin, X.; Zhang, S.; Xiu, H.; Pan, C.; Cui, W. A protective role of glibenclamide in inflammation-associated injury. Mediat. Inflamm., 2017, 3578702.
- Marchetti, C.; Chojnacki, J.; Toldo, S.; Mezzaroma, E.; Tranchida, N.; Rose, S.W.; Federici, M.; Van Tassell, B.W.; Zhang, S.; Abbate, A. A novel pharmacologic inhibitor of the NLRP3 inflammasome limits myocardial injury after ischemia-reperfusion in the mouse. J. Cardiovasc. Pharmacol., 2014, 63(4), 316-322. doi: 10.1097/FJC.0000000000000053 PMID: 24336017
- Marchetti, C.; Toldo, S.; Chojnacki, J.; Mezzaroma, E.; Liu, K.; Salloum, F.N.; Nordio, A.; Carbone, S.; Mauro, A.G.; Das, A.; Zalavadia, A.A.; Halquist, M.S.; Federici, M.; Van Tassell, B.W.; Zhang, S.; Abbate, A. Pharmacologic inhibition of the NLRP3 inflammasome preserves cardiac function after ischemic and nonischemic injury in the mouse. J. Cardiovasc. Pharmacol., 2015, 66(1), 1-8. doi: 10.1097/FJC.0000000000000247 PMID: 25915511
- Guo, C.; Fulp, J.W.; Jiang, Y.; Li, X.; Chojnacki, J.E.; Wu, J.; Wang, X.Y.; Zhang, S. Development and characterization of a hydroxyl-sulfonamide analogue, 5-chloro-N-2-(4-hydroxysulfamoyl-phenyl)-ethyl-2-methoxy-benzamide, as a novel NLRP3 inflammasome inhibitor for potential treatment of multiple sclerosis. ACS Chem. Neurosci., 2017, 8(10), 2194-2201. doi: 10.1021/acschemneuro.7b00124 PMID: 28653829
- Yin, J.; Zhao, F.; Chojnacki, J.E.; Fulp, J.; Klein, W.L.; Zhang, S.; Zhu, X. NLRP3 inflammasome inhibitor ameliorates amyloid pathology in a mouse model of Alzheimers disease. Mol. Neurobiol., 2018, 55(3), 1977-1987. doi: 10.1007/s12035-017-0467-9 PMID: 28255908
- Kuwar, R.; Rolfe, A.; Di, L.; Xu, H.; He, L.; Jiang, Y.; Zhang, S.; Sun, D. A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury. J. Neuroinflammation, 2019, 16(1), 81. doi: 10.1186/s12974-019-1471-y PMID: 30975164
- Fulp, J.; He, L.; Toldo, S.; Jiang, Y.; Boice, A.; Guo, C.; Li, X.; Rolfe, A.; Sun, D.; Abbate, A.; Wang, X.Y.; Zhang, S. Structural insights of benzenesulfonamide analogues as NLRP3 inflammasome inhibitors: Design, synthesis, and biological characterization. J. Med. Chem., 2018, 61(12), 5412-5423. doi: 10.1021/acs.jmedchem.8b00733 PMID: 29877709
- Jiang, Y.; He, L.; Green, J.; Blevins, H.; Guo, C.; Patel, S.H.; Halquist, M.S.; McRae, M.; Venitz, J.; Wang, X.Y.; Zhang, S. Discovery of second-generation NLRP3 inflammasome inhibitors: Design, synthesis, and biological characterization. J. Med. Chem., 2019, 62(21), 9718-9731. doi: 10.1021/acs.jmedchem.9b01155 PMID: 31626545
- Xu, Y.; Xu, Y.; Blevins, H.; Guo, C.; Biby, S.; Wang, X.Y.; Wang, C.; Zhang, S. Development of sulfonamide-based NLRP3 inhibitors: Further modifications and optimization through structure-activity relationship studies. Eur. J. Med. Chem., 2022, 238, 114468. doi: 10.1016/j.ejmech.2022.114468 PMID: 35635948
- Perregaux, D.G.; McNiff, P.; Laliberte, R.; Hawryluk, N.; Peurano, H.; Stam, E.; Eggler, J.; Griffiths, R.; Dombroski, M.A.; Gabel, C.A. Identification and characterization of a novel class of interleukin-1 post-translational processing inhibitors. J. Pharmacol. Exp. Ther., 2001, 299(1), 187-197. PMID: 11561079
- Laliberte, R.E.; Perregaux, D.G.; Hoth, L.R.; Rosner, P.J.; Jordan, C.K.; Peese, K.M.; Eggler, J.F.; Dombroski, M.A.; Geoghegan, K.F.; Gabel, C.A. Glutathione s-transferase omega 1-1 is a target of cytokine release inhibitory drugs and may be responsible for their effect on interleukin-1β posttranslational processing. J. Biol. Chem., 2003, 278(19), 16567-16578. doi: 10.1074/jbc.M211596200 PMID: 12624100
- Coll, R.C.; ONeill, L.A.J.; Butler, M.; Cooper, M.; ONeill, L.A. The cytokine release inhibitory drug CRID3 targets ASC oligomerisation in the NLRP3 and AIM2 inflammasomes. PLoS One, 2011, 6(12), e29539. doi: 10.1371/journal.pone.0029539 PMID: 22216309
- Tapia-Abellán, A.; Angosto-Bazarra, D.; Martínez-Banaclocha, H.; de Torre-Minguela, C.; Cerón-Carrasco, J.P.; Pérez-Sánchez, H.; Arostegui, J.I.; Pelegrin, P. MCC950 closes the active conformation of NLRP3 to an inactive state. Nat. Chem. Biol., 2019, 15(6), 560-564. doi: 10.1038/s41589-019-0278-6 PMID: 31086329
- Coll, R.C.; Hill, J.R.; Day, C.J.; Zamoshnikova, A.; Boucher, D.; Massey, N.L.; Chitty, J.L.; Fraser, J.A.; Jennings, M.P.; Robertson, A.A.B.; Schroder, K. MCC950 directly targets the NLRP3 ATP-hydrolysis motif for inflammasome inhibition. Nat. Chem. Biol., 2019, 15(6), 556-559. doi: 10.1038/s41589-019-0277-7 PMID: 31086327
- Corcoran, S.E.; Halai, R.; Cooper, M.A. Pharmacological inhibition of the Nod-Like receptor family pyrin domain containing 3 inflammasome with MCC950. Pharmacol. Rev., 2021, 73(3), 968-1000. doi: 10.1124/pharmrev.120.000171 PMID: 34117094
- Salla, M.; Butler, M.S.; Pelingon, R.; Kaeslin, G.; Croker, D.E.; Reid, J.C.; Baek, J.M.; Bernhardt, P.V.; Gillam, E.M.J.; Cooper, M.A.; Robertson, A.A.B. Identification, synthesis, and biological evaluation of the major human metabolite of NLRP3 inflammasome inhibitor MCC950. ACS Med. Chem. Lett., 2016, 7(12), 1034-1038. doi: 10.1021/acsmedchemlett.6b00198 PMID: 27994733
- Li, H.; Guan, Y.; Liang, B.; Ding, P.; Hou, X.; Wei, W.; Ma, Y. Therapeutic potential of MCC950, a specific inhibitor of NLRP3 inflammasome. Eur. J. Pharmacol., 2022, 928, 175091. doi: 10.1016/j.ejphar.2022.175091 PMID: 35714692
- Hill, J.R.; Coll, R.C.; Sue, N.; Reid, J.C.; Dou, J.; Holley, C.L.; Pelingon, R.; Dickinson, J.B.; Biden, T.J.; Schroder, K.; Cooper, M.A.; Robertson, A.A.B. Sulfonylureas as concomitant insulin secretagogues and NLRP3 inflammasome inhibitors. ChemMedChem, 2017, 12(17), 1449-1457. doi: 10.1002/cmdc.201700270 PMID: 28703484
- Agarwal, S.; Pethani, J.P.; Shah, H.A.; Vyas, V.; Sasane, S.; Bhavsar, H.; Bandyopadhyay, D.; Giri, P.; Viswanathan, K.; Jain, M.R.; Sharma, R. Identification of a novel orally bioavailable NLRP3 inflammasome inhibitor. Bioorg. Med. Chem. Lett., 2020, 30(21), 127571. doi: 10.1016/j.bmcl.2020.127571 PMID: 32980515
- McBride, C.; Trzoss, L.; Povero, D.; Lazic, M.; Ambrus-Aikelin, G.; Santini, A.; Pranadinata, R.; Bain, G.; Stansfield, R.; Stafford, J.A.; Veal, J.; Takahashi, R.; Ly, J.; Chen, S.; Liu, L.; Nespi, M.; Blake, R.; Katewa, A.; Kleinheinz, T.; Sujatha-Bhaskar, S.; Ramamoorthi, N.; Sims, J.; McKenzie, B.; Chen, M.; Ultsch, M.; Johnson, M.; Murray, J.; Ciferri, C.; Staben, S.T.; Townsend, M.J.; Stivala, C.E. Overcoming Preclinical Safety Obstacles to Discover (S)- N -((1,2,3,5,6,7-Hexahydro- s -indacen-4-yl)carbamoyl)-6-(methylamino)-6,7-dihydro-5 H -pyrazolo5,1- b1,3oxazine-3-sulfonamide (GDC-2394): A Potent and Selective NLRP3 Inhibitor. J. Med. Chem., 2022, 65(21), 14721-14739. doi: 10.1021/acs.jmedchem.2c01250 PMID: 36279149
- Agarwal, S.; Sasane, S.; Shah, H.A.; Pethani, J.P.; Deshmukh, P.; Vyas, V.; Iyer, P.; Bhavsar, H.; Viswanathan, K.; Bandyopadhyay, D.; Giri, P.; Mahapatra, J.; Chatterjee, A.; Jain, M.R.; Sharma, R. Discovery of N-cyano-sulfoximineurea derivatives as potent and orally bioavailable NLRP3 inflammasome inhibitors. ACS Med. Chem. Lett., 2020, 11(4), 414-418. doi: 10.1021/acsmedchemlett.9b00433 PMID: 32292543
- Harrison, D.; Boutard, N.; Brzozka, K.; Bugaj, M.; Chmielewski, S.; Cierpich, A.; Doedens, J.R.; Fabritius, C.H.R.Y.; Gabel, C.A.; Galezowski, M.; Kowalczyk, P.; Levenets, O.; Mroczkowska, M.; Palica, K.; Porter, R.A.; Schultz, D.; Sowinska, M.; Topolnicki, G.; Urbanski, P.; Woyciechowski, J.; Watt, A.P. Discovery of a series of ester-substituted NLRP3 inflammasome inhibitors. Bioorg. Med. Chem. Lett., 2020, 30(23), 127560. doi: 10.1016/j.bmcl.2020.127560 PMID: 32956781
- Albanese, V.; Missiroli, S.; Perrone, M.; Fabbri, M.; Boncompagni, C.; Pacifico, S.; De Ventura, T.; Ciancetta, A.; Dondio, G.; Kricek, F.; Pinton, P.; Guerrini, R.; Preti, D.; Giorgi, C. Novel aryl sulfonamide derivatives as NLRP3 inflammasome inhibitors for the potential treatment of cancer. J. Med. Chem., 2023, 66(7), 5223-5241. doi: 10.1021/acs.jmedchem.3c00175 PMID: 36972104
- Li, W.; Cao, Z.; Cheng, J.; Chen, F.; Li, S.; Huang, Y.; Zheng, L.T.; Ye, N. Discovery of N-phenyl-1-(phenylsulfonamido)cyclopropane-1-carboxamide analogs as NLRP3 inflammasome inhibitors. Med. Chem. Res., 2021, 30(6), 1294-1308. doi: 10.1007/s00044-021-02740-7
- Narros-Fernández, P.; Chioua, M.; Petcu, S.A.; Diez-Iriepa, D.; Cerrada-Gálvez, L.; Decouty-Pérez, C.; Palomino-Antolín, A.; Ramos, E.; Farré-Alins, V.; López-Rodríguez, A.B.; Romero, A.; Marco-Contelles, J.; Egea, J. Synthesis and pharmacological evaluation of new N-sulfonylureas as NLRP3 inflammasome inhibitors: Identification of a hit compound to treat gout. J. Med. Chem., 2022, 65(8), 6250-6260. doi: 10.1021/acs.jmedchem.2c00149 PMID: 35403430
- Harrison, D.; Bock, M.G.; Doedens, J.R.; Gabel, C.A.; Holloway, M.K.; Lewis, A.; Scanlon, J.; Sharpe, A.; Simpson, I.D.; Smolak, P.; Wishart, G.; Watt, A.P. Discovery and optimization of triazolopyrimidinone derivatives as selective NLRP3 inflammasome inhibitors. ACS Med. Chem. Lett., 2022, 13(8), 1321-1328. doi: 10.1021/acsmedchemlett.2c00242 PMID: 35978696
- Ma, T.; Thiagarajah, J.R.; Yang, H.; Sonawane, N.D.; Folli, C.; Galietta, L.J.V.; Verkman, A.S. Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxininduced intestinal fluid secretion. J. Clin. Invest., 2002, 110(11), 1651-1658. doi: 10.1172/JCI0216112 PMID: 12464670
- Jiang, H.; He, H.; Chen, Y.; Huang, W.; Cheng, J.; Ye, J.; Wang, A.; Tao, J.; Wang, C.; Liu, Q.; Jin, T.; Jiang, W.; Deng, X.; Zhou, R. Identification of a selective and direct NLRP3 inhibitor to treat inflammatory disorders. J. Exp. Med., 2017, 214(11), 3219-3238. doi: 10.1084/jem.20171419 PMID: 29021150
- Chen, Y.; He, H.; Jiang, H.; Li, L.; Hu, Z.; Huang, H.; Xu, Q.; Zhou, R.; Deng, X. Discovery and optimization of 4-oxo-2-thioxo-thiazolidinones as NOD-like receptor (NLR) family, pyrin domain-containing protein 3 (NLRP3) inhibitors. Bioorg. Med. Chem. Lett., 2020, 30(7), 127021. doi: 10.1016/j.bmcl.2020.127021 PMID: 32057583
- Zuo, D.; Do, N.; Hwang, I.; Ann, J.; Yu, J.W.; Lee, J. Design and synthesis of an N-benzyl 5-(4-sulfamoylbenzylidene-2-thioxothiazolidin-4-one scaffold as a novel NLRP3 inflammasome inhibitor. Bioorg. Med. Chem. Lett., 2022, 65, 128693. doi: 10.1016/j.bmcl.2022.128693 PMID: 35314328
- Liu, W.; Guo, W.; Wu, J.; Luo, Q.; Tao, F.; Gu, Y.; Shen, Y.; Li, J.; Tan, R.; Xu, Q.; Sun, Y. A novel benzodimidazole derivate prevents the development of dextran sulfate sodium-induced murine experimental colitis via inhibition of NLRP3 inflammasome. Biochem. Pharmacol., 2013, 85(10), 1504-1512. doi: 10.1016/j.bcp.2013.03.008 PMID: 23506741
- Pan, L.; Hang, N.; Zhang, C.; Chen, Y.; Li, S.; Sun, Y.; Li, Z.; Meng, X. Synthesis and biological evaluation of novel benzimidazole derivatives and analogs targeting the NLRP3 inflammasome. Molecules, 2017, 22(2), 213. doi: 10.3390/molecules22020213 PMID: 28146092
- Chen, H.; Chen, X.; Sun, P.; Wu, D.; Yue, H.; Pan, J.; Li, X.; Zhang, C.; Wu, X.; Hua, L.; Hu, W.; Yang, Z. Discovery of dronedarone and its analogues as NLRP3 inflammasome inhibitors with potent anti-inflammation activity. Bioorg. Med. Chem. Lett., 2021, 46, 128160. doi: 10.1016/j.bmcl.2021.128160 PMID: 34062252
- Huang, Y.; Jiang, H.; Chen, Y.; Wang, X.; Yang, Y.; Tao, J.; Deng, X.; Liang, G.; Zhang, H.; Jiang, W.; Zhou, R. Tranilast directly targets NLRP 3 to treat inflammasome-driven diseases. EMBO Mol. Med., 2018, 10(4), e8689. doi: 10.15252/emmm.201708689 PMID: 29531021
- Zhuang, T.; Li, S.; Yi, X.; Guo, S.; Wang, Y.; Chen, J.; Liu, L.; Jian, Z.; Gao, T.; Kang, P.; Li, C. Tranilast directly targets NLRP3 to protect melanocytes from keratinocyte-derived IL-1β under oxidative stress. Front. Cell Dev. Biol., 2020, 8, 588. doi: 10.3389/fcell.2020.00588 PMID: 32754591
- Abdullaha, M.; Ali, M.; Kour, D.; Kumar, A.; Bharate, S.B. Discovery of benzocdindol-2-one and benzylidene-thiazolidine-2,4-dione as new classes of NLRP3 inflammasome inhibitors via ER-β structure based virtual screening. Bioorg. Chem., 2020, 95, 103500. doi: 10.1016/j.bioorg.2019.103500 PMID: 31869665
- Abdullaha, M.; Ali, M.; Kour, D.; Mudududdla, R.; Khajuria, P.; Kumar, A.; Bharate, S.B. Tetramethoxystilbene inhibits NLRP3 inflammasome assembly via blocking the oligomerization of apoptosis-associated speck-like protein containing caspase recruitment domain: In vitro and in vivo evaluation. ACS Pharmacol. Transl. Sci., 2021, 4(4), 1437-1448. doi: 10.1021/acsptsci.1c00126 PMID: 34423275
- Sebastian-Valverde, M.; Wu, H.; Al Rahim, M.; Sanchez, R.; Kumar, K.; De Vita, R.J.; Pasinetti, G.M. Discovery and characterization of small-molecule inhibitors of NLRP3 and NLRC4 inflammasomes. J. Biol. Chem., 2021, 296, 100597. doi: 10.1016/j.jbc.2021.100597 PMID: 33781745
- Dai, Z.; Chen, X.; An, L.; Li, C.; Zhao, N.; Yang, F.; You, S.; Hou, C.; Li, K.; Jiang, C.; You, Q.; Di, B.; Xu, L. Development of novel tetrahydroquinoline inhibitors of NLRP3 inflammasome for potential treatment of DSS-induced mouse colitis. J. Med. Chem., 2021, 64(1), 871-889. doi: 10.1021/acs.jmedchem.0c01924 PMID: 33332136
- Baldwin, A.G.; Rivers-Auty, J.; Daniels, M.J.D.; White, C.S.; Schwalbe, C.H.; Schilling, T.; Hammadi, H.; Jaiyong, P.; Spencer, N.G.; England, H.; Luheshi, N.M.; Kadirvel, M.; Lawrence, C.B.; Rothwell, N.J.; Harte, M.K.; Bryce, R.A.; Allan, S.M.; Eder, C.; Freeman, S.; Brough, D. Boron-based inhibitors of the NLRP3 inflammasome. Cell Chem. Biol., 2017, 24(11), 1321-1335.e5. doi: 10.1016/j.chembiol.2017.08.011 PMID: 28943355
- Jiao, Y.; Nan, J.; Mu, B.; Zhang, Y.; Zhou, N.; Yang, S.; Zhang, S.; Lin, W.; Wang, F.; Xia, A.; Cao, Z.; Chen, P.; Pan, Z.; Lin, G.; Pan, S.; Bin, H.; Li, L.; Yang, S. Discovery of a novel and potent inhibitor with differential species-specific effects against NLRP3 and AIM2 inflammasome-dependent pyroptosis. Eur. J. Med. Chem., 2022, 232, 114194. doi: 10.1016/j.ejmech.2022.114194 PMID: 35183871
- Abdullaha, M.; Mohammed, S.; Ali, M.; Kumar, A.; Vishwakarma, R.A.; Bharate, S.B. Discovery of quinazolin-4(3H)-ones as NLRP3 inflammasome inhibitors: Computational design, metal-free synthesis, and in vitro biological evaluation. J. Org. Chem., 2019, 84(9), 5129-5140. doi: 10.1021/acs.joc.9b00138 PMID: 30896160
- Liao, K.C.; Sandall, C.F.; Carlson, D.A.; Ulke-Lemée, A.; Platnich, J.M.; Hughes, P.F.; Muruve, D.A.; Haystead, T.A.J.; MacDonald, J.A. Application of immobilized ATP to the study of NLRP inflammasomes. Arch. Biochem. Biophys., 2019, 670, 104-115. doi: 10.1016/j.abb.2018.12.031 PMID: 30641048
- Gastaldi, S.; Boscaro, V.; Gianquinto, E.; Sandall, C.F.; Giorgis, M.; Marini, E.; Blua, F.; Gallicchio, M.; Spyrakis, F.; MacDonald, J.A.; Bertinaria, M. Chemical modulation of the 1-(piperidin-4-yl)-1,3-dihydro-2H-benzod imidazole-2-one scaffold as a novel NLRP3 inhibitor. Molecules, 2021, 26(13), 3975. doi: 10.3390/molecules26133975 PMID: 34209843
- Haseeb, M.; Javaid, N.; Yasmeen, F.; Jeong, U.; Han, J.H.; Yoon, J.; Seo, J.Y.; Heo, J.K.; Shin, H.C.; Kim, M.S.; Kim, W.; Choi, S. Novel small-molecule inhibitor of NLRP3 inflammasome reverses cognitive impairment in an Alzheimers disease model. ACS Chem. Neurosci., 2022, 13(6), 818-833. doi: 10.1021/acschemneuro.1c00831 PMID: 35196855
- Cocco, M.; Garella, D.; Di Stilo, A.; Borretto, E.; Stevanato, L.; Giorgis, M.; Marini, E.; Fantozzi, R.; Miglio, G.; Bertinaria, M. Electrophilic warhead-based design of compounds preventing NLRP3 inflammasome-dependent pyroptosis. J. Med. Chem., 2014, 57(24), 10366-10382. doi: 10.1021/jm501072b PMID: 25418070
- Cocco, M.; Miglio, G.; Giorgis, M.; Garella, D.; Marini, E.; Costale, A.; Regazzoni, L.; Vistoli, G.; Orioli, M.; Massulaha-Ahmed, R.; Détraz-Durieux, I.; Groslambert, M.; Py, B.F.; Bertinaria, M. Design, synthesis, and evaluation of acrylamide derivatives as direct NLRP3 inflammasome inhibitors. ChemMedChem, 2016, 11(16), 1790-1803. doi: 10.1002/cmdc.201600055 PMID: 26990578
- Cocco, M.; Pellegrini, C.; Martínez-Banaclocha, H.; Giorgis, M.; Marini, E.; Costale, A.; Miglio, G.; Fornai, M.; Antonioli, L.; López-Castejón, G.; Tapia-Abellán, A.; Angosto, D.; Hafner-Bratkovič, I.; Regazzoni, L.; Blandizzi, C.; Pelegrín, P.; Bertinaria, M. Development of an acrylate derivative targeting the NLRP3 inflammasome for the treatment of inflammatory bowel disease. J. Med. Chem., 2017, 60(9), 3656-3671. doi: 10.1021/acs.jmedchem.6b01624 PMID: 28410442
- Juliana, C.; Fernandes-Alnemri, T.; Wu, J.; Datta, P.; Solorzano, L.; Yu, J.W.; Meng, R.; Quong, A.A.; Latz, E.; Scott, C.P.; Alnemri, E.S. Anti-inflammatory compounds parthenolide and Bay 11-7082 are direct inhibitors of the inflammasome. J. Biol. Chem., 2010, 285(13), 9792-9802. doi: 10.1074/jbc.M109.082305 PMID: 20093358
- Zhang, X.; Xu, A.; Ran, Y.; Wei, C.; Xie, F.; Wu, J. Design, synthesis and biological evaluation of phenyl vinyl sulfone based NLRP3 inflammasome inhibitors. Bioorg. Chem., 2022, 128, 106010. doi: 10.1016/j.bioorg.2022.106010 PMID: 35914391
- Marchetti, C.; Swartzwelter, B.; Gamboni, F.; Neff, C.P.; Richter, K.; Azam, T.; Carta, S.; Tengesdal, I.; Nemkov, T.; DAlessandro, A.; Henry, C.; Jones, G.S.; Goodrich, S.A.; St Laurent, J.P.; Jones, T.M.; Scribner, C.L.; Barrow, R.B.; Altman, R.D.; Skouras, D.B.; Gattorno, M.; Grau, V.; Janciauskiene, S.; Rubartelli, A.; Joosten, L.A.B.; Dinarello, C.A. OLT1177, a β-sulfonyl nitrile compound, safe in humans, inhibits the NLRP3 inflammasome and reverses the metabolic cost of inflammation. Proc. Natl. Acad. Sci., 2018, 115(7), E1530-E1539. doi: 10.1073/pnas.1716095115 PMID: 29378952
- Lunding, L.P.; Skouras, D.B.; Vock, C.; Dinarello, C.A.; Wegmann, M. The NLRP3 inflammasome inhibitor, OLT1177®, ameliorates experimental allergic asthma in mice. Allergy, 2022, 77(3), 1035-1038. doi: 10.1111/all.15164 PMID: 34716997
- Marchetti, C.; Swartzwelter, B.; Koenders, M.I.; Azam, T.; Tengesdal, I.W.; Powers, N.; de Graaf, D.M.; Dinarello, C.A.; Joosten, L.A.B. NLRP3 inflammasome inhibitor OLT1177 suppresses joint inflammation in murine models of acute arthritis. Arthritis Res. Ther., 2018, 20(1), 169. doi: 10.1186/s13075-018-1664-2 PMID: 30075804
- Lonnemann, N.; Hosseini, S.; Marchetti, C.; Skouras, D.B.; Stefanoni, D.; DAlessandro, A.; Dinarello, C.A.; Korte, M. The NLRP3 inflammasome inhibitor OLT1177 rescues cognitive impairment in a mouse model of Alzheimers disease. Proc. Natl. Acad. Sci., 2020, 117(50), 32145-32154. doi: 10.1073/pnas.2009680117 PMID: 33257576
- He, Y.; Varadarajan, S.; Muñoz-Planillo, R.; Burberry, A.; Nakamura, Y.; Núñez, G. 3,4-methylenedioxy-β-nitrostyrene inhibits NLRP3 inflammasome activation by blocking assembly of the inflammasome. J. Biol. Chem., 2014, 289(2), 1142-1150. doi: 10.1074/jbc.M113.515080 PMID: 24265316
- Xiao, M.; Li, L.; Li, C.; Liu, L.; Yu, Y.; Ma, L. 3,4-Methylenedioxy-β-Nitrostyrene ameliorates experimental burn wound progression by inhibiting the NLRP3 inflammasome activation. Plast. Reconstr. Surg., 2016, 137(3), 566e-575e. doi: 10.1097/01.prs.0000479972.06934.83 PMID: 26910701
- Chen, Y.; He, H.; Lin, B.; Chen, Y.; Deng, X.; Jiang, W.; Zhou, R. RRx-001 ameliorates inflammatory diseases by acting as a potent covalent NLRP3 inhibitor. Cell. Mol. Immunol., 2021, 18(6), 1425-1436. doi: 10.1038/s41423-021-00683-y PMID: 33972740
- Jayabalan, N.; Oronsky, B.; Cabrales, P.; Reid, T.; Caroen, S.; Johnson, A.M.; Birch, N.A.; OSullivan, J.D.; Gordon, R. A review of RRx-001: A late-stage multi-indication inhibitor of NLRP3 activation and chronic inflammation. Drugs, 2023, 83(5), 389-402. doi: 10.1007/s40265-023-01838-z PMID: 36920652
- Shim, D.W.; Shin, W.Y.; Yu, S.H.; Kim, B.H.; Ye, S.K.; Koppula, S.; Won, H.S.; Kang, T.B.; Lee, K.H. BOT-4-one attenuates NLRP3 inflammasome activation: NLRP3 alkylation leading to the regulation of its ATPase activity and ubiquitination. Sci. Rep., 2017, 7(1), 15020. doi: 10.1038/s41598-017-15314-8 PMID: 29118366
- Ou, Y.; Sun, P.; Wu, N.; Chen, H.; Wu, D.; Hu, W.; Yang, Z. Synthesis and biological evaluation of parthenolide derivatives with reduced toxicity as potential inhibitors of the NLRP3 inflammasome. Bioorg. Med. Chem. Lett., 2020, 30(17), 127399. doi: 10.1016/j.bmcl.2020.127399 PMID: 32738997
- Chen, L.Z.; Zhang, X.X.; Liu, M.M.; Wu, J.; Ma, D.; Diao, L.Z.; Li, Q.; Huang, Y.S.; Zhang, R.; Ruan, B.F.; Liu, X.H. Discovery of novel pterostilbene-based derivatives as potent and orally active NLRP3 inflammasome inhibitors with inflammatory activity for colitis. J. Med. Chem., 2021, 64(18), 13633-13657. doi: 10.1021/acs.jmedchem.1c01007 PMID: 34506712
- Zhang, X.X.; Diao, L.Z.; Chen, L.Z.; Ma, D.; Wang, Y.M.; Jiang, H.; Ruan, B.F.; Liu, X.H. Discovery of 4-((E)-3,5-dimethoxy-2-((E)-2-nitrovinyl)styryl)aniline derivatives as potent and orally active NLRP3 inflammasome inhibitors for colitis. Eur. J. Med. Chem., 2022, 236, 114357. doi: 10.1016/j.ejmech.2022.114357 PMID: 35428012
- Ruan, B.; Rong, M.; Ming, Z.; Wang, K.; Liu, X.; Deng, L.; Zhang, X.; Xu, K.; Shi, C.; Gao, T.; Liu, X.; Chen, L. Discovery of pterostilbene analogs as novel NLRP3 inflammasome inhibitors for potential treatment of DSS-induced colitis in mice. Bioorg. Chem., 2023, 133, 106429. doi: 10.1016/j.bioorg.2023.106429 PMID: 36841048
- Zeng, Q.; Deng, H.; Li, Y.; Fan, T.; Liu, Y.; Tang, S.; Wei, W.; Liu, X.; Guo, X.; Jiang, J.; Wang, Y.; Song, D. Berberine directly targets the NEK7 protein to block the NEK7NLRP3 interaction and exert anti-inflammatory activity. J. Med. Chem., 2021, 64(1), 768-781. doi: 10.1021/acs.jmedchem.0c01743 PMID: 33440945
- Li, J.; Sheng, H.; Wang, Y.; Lai, Z.; Wang, Y.; Cui, S. Scaffold hybrid of the natural product tanshinone I with piperidine for the discovery of a potent NLRP3 inflammasome inhibitor. J. Med. Chem., 2023, 66(4), 2946-2963. doi: 10.1021/acs.jmedchem.2c01967 PMID: 36786612
- He, H.; Jiang, H.; Chen, Y.; Ye, J.; Wang, A.; Wang, C.; Liu, Q.; Liang, G.; Deng, X.; Jiang, W.; Zhou, R. Oridonin is a covalent NLRP3 inhibitor with strong anti-inflammasome activity. Nat. Commun., 2018, 9(1), 2550. doi: 10.1038/s41467-018-04947-6 PMID: 29959312
- Pang, L.; Liu, H.; Quan, H.; Sui, H.; Jia, Y. Development of novel oridonin analogs as specifically targeted NLRP3 inflammasome inhibitors for the treatment of dextran sulfate sodium-induced colitis. Eur. J. Med. Chem., 2023, 245(Pt 2), 114919. doi: 10.1016/j.ejmech.2022.114919 PMID: 36399877
- Thapa, P.; Upadhyay, S.P.; Singh, V.; Boinpelly, V.C.; Zhou, J.; Johnson, D.K.; Gurung, P.; Lee, E.S.; Sharma, R.; Sharma, M. Chalcone: A potential scaffold for NLRP3 inflammasome inhibitors. Europ. J. Med. Chem. Rep., 2023, 7, 100100. doi: 10.1016/j.ejmcr.2022.100100 PMID: 37033416
- Wang, K.; Lv, Q.; Miao, Y.; Qiao, S.; Dai, Y.; Wei, Z. Cardamonin, a natural flavone, alleviates inflammatory bowel disease by the inhibition of NLRP3 inflammasome activation via an AhR/Nrf2/NQO1 pathway. Biochem. Pharmacol., 2018, 155, 494-509. doi: 10.1016/j.bcp.2018.07.039 PMID: 30071202
- Leu, W.J.; Chu, J.C.; Hsu, J.L.; Du, C.M.; Jiang, Y.H.; Hsu, L.C.; Huang, W.J.; Guh, J.H. Chalcones display anti-NLRP3 inflammasome activity in macrophages through inhibition of both priming and activation Steps-structure-activity-relationship and mechanism studies. Molecules, 2020, 25(24), 5960. doi: 10.3390/molecules25245960 PMID: 33339319
- Tang, Y.L.; Zheng, X.; Qi, Y.; Pu, X.J.; Liu, B.; Zhang, X.; Li, X.S.; Xiao, W.L.; Wan, C.P.; Mao, Z.W. Synthesis and anti-inflammatory evaluation of new chalcone derivatives bearing bispiperazine linker as IL-1β inhibitors. Bioorg. Chem., 2020, 98, 103748. doi: 10.1016/j.bioorg.2020.103748 PMID: 32179281
- Zhang, C.; Yue, H.; Sun, P.; Hua, L.; Liang, S.; Ou, Y.; Wu, D.; Wu, X.; Chen, H.; Hao, Y.; Hu, W.; Yang, Z. Discovery of chalcone analogues as novel NLRP3 inflammasome inhibitors with potent anti-inflammation activities. Eur. J. Med. Chem., 2021, 219, 113417. doi: 10.1016/j.ejmech.2021.113417 PMID: 33845232
- Ma, X.; Zhao, M.; Tang, M.H.; Xue, L.L.; Zhang, R.J.; Liu, L.; Ni, H.F.; Cai, X.Y.; Kuang, S.; Hong, F.; Wang, L.; Chen, K.; Tang, H.; Li, Y.; Peng, A.H.; Yang, J.H.; Pei, H.Y.; Ye, H.Y.; Chen, L.J. Flavonoids with inhibitory effects on NLRP3 inflammasome activation from millettia velutina. J. Nat. Prod., 2020, 83(10), 2950-2959. doi: 10.1021/acs.jnatprod.0c00478 PMID: 32989985
- Zhang, R.; Hong, F.; Zhao, M.; Cai, X.; Jiang, X.; Ye, N.; Su, K.; Li, N.; Tang, M.; Ma, X.; Ni, H.; Wang, L.; Wan, L.; Chen, L.; Wu, W.; Ye, H. New highly potent NLRP3 inhibitors: Furanochalcone velutone F analogues. ACS Med. Chem. Lett., 2022, 13(4), 560-569. doi: 10.1021/acsmedchemlett.1c00597 PMID: 35450356
- Li, Q.; Feng, H.; Wang, H.; Wang, Y.; Mou, W.; Xu, G.; Zhang, P.; Li, R.; Shi, W.; Wang, Z.; Fang, Z.; Ren, L.; Wang, Y.; Lin, L.; Hou, X.; Dai, W.; Li, Z.; Wei, Z.; Liu, T.; Wang, J.; Guo, Y.; Li, P.; Zhao, X.; Zhan, X.; Xiao, X.; Bai, Z. Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7-NLRP3 interaction. EMBO Rep., 2022, 23(2), e53499. doi: 10.15252/embr.202153499 PMID: 34882936
- Gong, Z.; Zhao, S.; Zhou, J.; Yan, J.; Wang, L.; Du, X.; Li, H.; Chen, Y.; Cai, W.; Wu, J. Curcumin alleviates DSS-induced colitis via inhibiting NLRP3 inflammsome activation and IL-1β production. Mol. Immunol., 2018, 104, 11-19. doi: 10.1016/j.molimm.2018.09.004 PMID: 30396035
- Zhang, X.; Hu, L.; Xu, S.; Ye, C.; Chen, A. Erianin: A direct NLRP3 inhibitor with remarkable anti-Inflammatory activity. Front. Immunol., 2021, 12, 739953. doi: 10.3389/fimmu.2021.739953 PMID: 34745110
- Wang, H.; Lin, X.; Huang, G.; Zhou, R.; Lei, S.; Ren, J.; Zhang, K.; Feng, C.; Wu, Y.; Tang, W. Atranorin inhibits NLRP3 inflammasome activation by targeting ASC and protects NLRP3 inflammasome-driven diseases. Acta Pharmacol. Sin., 2023, 44(8), 1687-1700. doi: 10.1038/s41401-023-01054-1 PMID: 36964308
- Xu, H.; Chen, J.; Chen, P.; Li, W.; Shao, J.; Hong, S.; Wang, Y.; Chen, L.; Luo, W.; Liang, G. Costunolide covalently targets NACHT domain of NLRP3 to inhibit inflammasome activation and alleviate NLRP3-driven inflammatory diseases. Acta Pharm. Sin. B, 2023, 13(2), 678-693. doi: 10.1016/j.apsb.2022.09.014 PMID: 36873170
- Xu, H.; Li, W.; Hong, S.; Shao, J.; Chen, J.; Chattipakorn, N.; Wu, D.; Luo, W.; Liang, G. Tabersonine, a natural NLRP3 inhibitor, suppresses inflammasome activation in macrophages and attenuate NLRP3-driven diseases in mice. Acta Pharmacol. Sin., 2022, 0, 1-10. PMID: 36627344
- Li, W.; Xu, H.; Shao, J.; Chen, J.; Lin, Y.; Zheng, Z.; Wang, Y.; Luo, W.; Liang, G. Discovery of alantolactone as a naturally occurring NLRP3 inhibitor to alleviate NLRP3‐driven inflammatory diseases in mice. Br. J. Pharmacol., 2023, 180(12), 1634-1647. doi: 10.1111/bph.16036 PMID: 36668704
- Zhang, A.H.; Liu, W.; Jiang, N.; Xu, Q.; Tan, R.X. Spirodalesol, an NLRP3 inflammasome activation inhibitor. Org. Lett., 2016, 18(24), 6496-6499. doi: 10.1021/acs.orglett.6b03435 PMID: 27978645
- Liu, W.; Yang, J.; Fang, S.; Jiao, C.; Gao, J.; Zhang, A.; Wu, T.; Tan, R.; Xu, Q.; Guo, W. Spirodalesol analog 8A inhibits NLRP3 inflammasome activation and attenuates inflammatory disease by directly targeting adaptor protein ASC. J. Biol. Chem., 2022, 298(12), 102696. doi: 10.1016/j.jbc.2022.102696 PMID: 36379253
- Cui, W.; Chen, S.; Chi, Z.; Guo, X.; Zhang, X.; Zhong, Y.; Han, H.; Yao, K. Screening-based identification of xanthone as a novel NLRP3 inflammasome inhibitor via metabolic reprogramming. Clin. Transl. Med., 2021, 11(7), e496. doi: 10.1002/ctm2.496 PMID: 34323410
- Ahmed, S.; Kwatra, M.; Ranjan Panda, S.; Murty, U.S.N.; Naidu, V.G.M. Andrographolide suppresses NLRP3 inflammasome activation in microglia through induction of parkin-mediated mitophagy in in-vitro and in-vivo models of Parkinson disease. Brain Behav. Immun., 2021, 91, 142-158. doi: 10.1016/j.bbi.2020.09.017 PMID: 32971182
- González-Cofrade, L.; Oramas-Royo, S.; Cuadrado, I.; Amesty, Á.; Hortelano, S.; Estevez-Braun, A.; de las Heras, B. Dehydrohispanolone derivatives attenuate the inflammatory response through the modulation of inflammasome activation. J. Nat. Prod., 2020, 83(7), 2155-2164. doi: 10.1021/acs.jnatprod.0c00200 PMID: 32584575
- Bi, D.W.; Xiong, F.; Cheng, B.; Zhou, Y.L.; Zeb, M.A.; Tang, P.; Pang, W.H.; Zhang, R.H.; Li, X.L.; Zhang, X.J.; Xiao, W.L. Callintegers A and B, unusual tricyclo 4.4.0.09,10tetradecane clerodane diterpenoids from callicarpa integerrima with inhibitory effects on NLRP3 inflammasome activation. J. Nat. Prod., 2022, 85(11), 2675-2681. doi: 10.1021/acs.jnatprod.2c00568 PMID: 36286259
- Pu, D.B.; Zhang, X.J.; Bi, D.W.; Gao, J.B.; Yang, Y.; Li, X.L.; Lin, J.; Li, X.N.; Zhang, R.H.; Xiao, W.L. Callicarpins, Two classes of rearranged ent-clerodane diterpenoids from callicarpa plants blocking NLRP3 inflammasome-induced pyroptosis. J. Nat. Prod., 2020, 83(7), 2191-2199. doi: 10.1021/acs.jnatprod.0c00288 PMID: 32628479
- González-Cofrade, L.; P Green, J.; Cuadrado, I.; Amesty, Á.; Oramas-Royo, S.; David, Brough; Estévez-Braun, A.; Hortelano, S.; de Las Heras, B. Phenolic and quinone methide nor-triterpenes as selective NLRP3 inflammasome inhibitors. Bioorg. Chem., 2023, 132, 106362. doi: 10.1016/j.bioorg.2023.106362 PMID: 36657273
- Chen, C.; Liu, X.; Gong, L.; Zhu, T.; Zhou, W.; Kong, L.; Luo, J. Identification of Tubocapsanolide A as a novel NLRP3 inhibitor for potential treatment of colitis. Biochem. Pharmacol., 2021, 190, 114645. doi: 10.1016/j.bcp.2021.114645 PMID: 34090877
- Lin, G.; Li, N.; Li, D.; Chen, L.; Deng, H.; Wang, S.; Tang, J.; Ouyang, W. Carnosic acid inhibits NLRP3 inflammasome activation by targeting both priming and assembly steps. Int. Immunopharmacol., 2023, 116, 109819. doi: 10.1016/j.intimp.2023.109819 PMID: 36738671
- Shi, J.; Xia, Y.; Wang, H.; Yi, Z.; Zhang, R.; Zhang, X. Piperlongumine is an NLRP3 inhibitor with anti-inflammatory activity. Front. Pharmacol., 2022, 12, 818326. doi: 10.3389/fphar.2021.818326 PMID: 35095532
Қосымша файлдар
