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Gambogic acid suppresses nasopharyngeal carcinoma via rewiring molecular network of cancer malignancy and immunosurveillance.

Authors :
Ren, Tao
Bai, Xian-Yu
Yang, Meng-Zhe
Xu, Ning
Guo, Xing-Zhe
Qin, Liu-Jie
Huang, Zhi-Lin
Zhong, Qiong-Yao
Huang, Yuan-Jiao
Lin, Wen-Zhen
Jiao, Ai-Jun
Zhang, Bei-Bei
Source :
Biomedicine & Pharmacotherapy. Jun2022, Vol. 150, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Nasopharyngeal carcinoma (NPC) is a malignant tumor highly prevalent in Southeast Asia. The distant metastasis and disease recurrence are still unsolved clinical problems. In recent years, traditional Chinese medicine (TCM) monomers have become significantly attractive due to their advantages. Using high throughput drug sensitivity screening, we identified gambogic acid (GA) as a common TCM monomer displaying multiple anti-NPC effects. GA could effectively inhibit the proliferation of low differentiated cells and highly metastatic cells in NPC via inducing apoptosis and G2/M cell cycle arrest. In addition, GA obviously repressed the abilities of cell clone, migration, invasion, angiogenesis and represented satisfied synergistic effects combined with chemotherapy. Importantly, we found the elevated immune checkpoint CD47 stimulated after chemotherapy was dramatically impaired by GA treatment. Mechanically, the network pharmacology analyses unraveled that the oncogenic signaling pathways including STATs were rewired by GA treatment. Taken together, our study reveals a molecular basis and provides a rationale for GA application as the treatment regime in NPC therapy in future. [Display omitted] • GA as a common TCM monomer displays anti-NPC effects. • GA could induce NPC cell apoptosis and G2/M cell cycle arrest. • GA supresses cell clone, migration, invasion, angiogenesis and displays synergistic effects with chemotherapy. • Enhanced CD47 stimulated by chemotherapy is impaired by GA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
150
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
157105398
Full Text :
https://doi.org/10.1016/j.biopha.2022.113012