4.3 Article

Radix Tetrastigma Extracts Enhance the Chemosensitivity in Triple-Negative Breast Cancer Via Inhibiting PI3K/Akt/mTOR-Mediated Autophagy

期刊

CLINICAL BREAST CANCER
卷 22, 期 2, 页码 89-97

出版社

CIG MEDIA GROUP, LP
DOI: 10.1016/j.clbc.2021.07.015

关键词

RTEs; PI3K/Akt/mTOR; TNBC; Breast cancer; Autophagy

类别

资金

  1. Youth Foundation for Natural Science of Zhejiang province [LQ17H270004]
  2. Fund Project for Public Welfare Technology Application Research of Zhejiang Province [LGF21H160015]
  3. Health and Family Planning Commission of Zhejiang province [2016KYB217]
  4. National Natural Science Foundation of China [81904032]

向作者/读者索取更多资源

This study investigated the effect of Radix Tetrastigma extracts (RTEs) on Taxol-induced autophagy and chemosensitivity in triple-negative breast cancer (TNBC). The results showed that RTEs enhanced the chemosensitivity of resistant TNBC cells to Taxol by inhibiting PI3K/Akt/mTOR-mediated autophagy.
Objective: Drug resistance in tumors is one of the major factors that leads to chemotherapy failure. This study aims to investigate the effect of Radix Tetrastigma extracts (RTEs) on Taxol-induced autophagy and the chemosensitivity against drug resistance in triple-negative breast cancer (TNBC). Methods: Taxol-resistant MDA-MB-468 (MDA-MB-468/Taxol) cells were induced and treated with RTEs and/or Taxol. Mice were subcutaneously inoculated with MDA-MB- 468/Taxol cells to establish xenograft models. The associated protein levels were measured by western blotting. Flow cytometry, CCK-8 and EdU assay were performed to detect cell apoptosis, viability, and proliferation, respectively. Results: In MDA-MB-468/Taxol cells, RTEs & Taxol treatment increased cell apoptosis, reduced cell viability and proliferation, upregulated anti-autophagy marker LC3I/LC3II ratio, and enhanced mTOR level. With RTEs & Taxol treatment, mTOR silencing downregulated LC3I/LC3II ratio, increased cell viability and proliferation, and reduced cell apoptosis, while mTOR overexpression showed the opposite results. PI3K inhibitor reduced AKT and mTOR levels, and the effects on cell activities were similar to the results of mTOR silencing. After RTEs & Taxol injection, xenograft tumor was smaller, and AKT, mTOR, LC3I/LC3II ratio and apoptotic marker cleaved caspase-3 were increased. Conclusion: RTEs enhanced the chemosensitivity of resistant TNBC cells to Taxol through inhibiting PI3K/Akt/mTOR-mediated autophagy.Micro: RTEs exerted anti-tumor effects in various cancers, and this study determined its role in TNBC. Taxol-resistant MDA-MB-468 cells were induced and xenograft models were established. We found that RTEs inhibited autophagy of MDA-MB-468/Taxol cells and reduced tumor growth. Inhibition of PI3K/Akt/mTOR pathway promoted autophagy of MDA-MB468/Taxol cells. We may provide a new potential strategy for TNBC treatment. (C) 2021 Elsevier Inc. All rights reserved.

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