Systems Pharmacology-Based Dissection of Anti-Cancer Mechanism of Traditional Chinese Herb .

Front Pharmacol

School of Pharmacy/Key Laboratory of Xinjiang Phytomedicine Resources and Utilization, Ministry of Education, Shihezi University, Xinjiang, China.

Published: June 2021

AI Article Synopsis

  • Cancer is a leading cause of death globally, and effective drug development is essential, with traditional Chinese medicine (SI) showing promising anti-cancer effects whose mechanisms are not fully understood.
  • Researchers used systems pharmacology to identify active compounds in SI and construct networks to analyze their targets and pathways related to cancer, resulting in the discovery of seven key compounds and 187 targets.
  • Experimental tests confirmed that four of these compounds can reduce cell proliferation and increase apoptosis in certain cancer cell lines, providing a basis for further research and potential drug development in modern medicine.

Article Abstract

Cancer has the highest mortality in humans worldwide, and the development of effective drugs remains a key issue. Traditional Chinese medicine (SI) exhibits a series of effects, such as anti-cancer, but the action mechanisms are still unclear. Here, systems pharmacology was applied to reveal its anti-cancer mechanism. First, we screened the active compounds of SI. Then, the compound-target network, target-disease network, and target-pathway network were constructed. DAVID was applied for GOBP analysis and KEGG pathway enrichment analysis on cancer-related targets. Seven potential compounds and 187 targets were identified. The target-disease classification network showed that compounds mainly regulated proteins related to cancer, nervous system diseases, and cardiovascular system diseases. Also, SI anti-tumor effect mainly associated with the regulation of NO production, angiogenesis, MAPK, and PKB from GOBP enrichment. Additionally, KEGG pathway enrichment indicated that targets involved in anti-inflammatory action, inhibiting angiogenesis and anti-proliferation or inducing apoptosis. Experimental validation showed that four active compounds could inhibit cell proliferation and promote apoptosis in A549 (except for kaempferol), PC-3, and C6 cells. This study not only provides experimental evidence for further research on SI in cancer treatment but also promotes the development of potential drugs of SI in modern medicine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267469PMC
http://dx.doi.org/10.3389/fphar.2021.678203DOI Listing

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