Bibliometric Analysis and Systemic Review of Cantharidin Research Worldwide
- Authors: He T.1, Duan C.2, Feng W.2, Ao J.2, Lu D.3, Li X.1, Zhang J.3
-
Affiliations:
- School of Basic Medicine,, Zunyi Medical University
- School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education, Zunyi Medical University
- School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education,, Zunyi Medical University
- Issue: Vol 25, No 12 (2024)
- Pages: 1585-1601
- Section: Biotechnology
- URL: https://rjpbr.com/1389-2010/article/view/645291
- DOI: https://doi.org/10.2174/0113892010244101231024111850
- ID: 645291
Cite item
Full Text
Abstract
Background:Cantharidin (CTD), a natural toxic compound from blister beetle Mylabris, has been used for cancer treatment for millenary. CTD and its analogs have become mainstream adjuvant drugs with radiotherapy and chemotherapy in clinical applications. However, the detailed pharmacology mechanism of CTD was not fully elucidated.
Methods:Publications of CTD were collected from the Web of Science Core Collection database from 1991 to 2023 using CiteSpace, VOSviewer, and Scimago Graphica software.
Results:A total of 1,611 publications of CTD were mainly published in China and the United States. The University of Newcastle has published the most researches. Mcclusey, Adam, Sakoff, Jennette, and Zhang, Yalin had the most CTD publications with higher H. Notably, CTD researches were mainly published in Bioorganic & Medicinal Chemistry Letters and the Journal of Biological Chemistry. Cluster profile results revealed that protein phosphatase 2A (PP2A), human gallbladder carcinoma, Aidi injection, and cell apoptosis were the hotspots. Concentration on the pharmacology function of PP2A subunit regulation, hepatotoxicity, nephrotoxicity, and cardiotoxicity mechanism should be strengthened in the future.
Conclusion:Bibliometric analysis combined with a systemic review of CTD research first revealed that PP2A and CTD analogs were the knowledge base of CTD, and PP2A subunit regulation and toxic mechanism could be the frontiers of CTD.
About the authors
Tianmu He
School of Basic Medicine,, Zunyi Medical University
Email: info@benthamscience.net
Cancan Duan
School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education, Zunyi Medical University
Email: info@benthamscience.net
Wenzhong Feng
School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education, Zunyi Medical University
Email: info@benthamscience.net
Jingwen Ao
School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education, Zunyi Medical University
Email: info@benthamscience.net
Dingyang Lu
School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education,, Zunyi Medical University
Email: info@benthamscience.net
Xiaofei Li
School of Basic Medicine,, Zunyi Medical University
Author for correspondence.
Email: info@benthamscience.net
Jianyong Zhang
School of Pharmacy and Key Laboratory of Basic Pharmacology Ministry Education and Joint International Research Laboratory of Ethnomedicine, Ministry of Education,, Zunyi Medical University
Author for correspondence.
Email: info@benthamscience.net
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