4.7 Article

Ethanol Extract ofBrucea javanicaSeed Inhibit Triple-Negative Breast Cancer by Restraining Autophagy via PI3K/Akt/mTOR Pathway

期刊

FRONTIERS IN PHARMACOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2020.00606

关键词

Brucea javanica; triple-negative breast cancer (TNBC); autophagy; PI3K; Akt; mTOR; toxicity

资金

  1. National Natural Science Foundation of China [81902709, 81872344]
  2. Natural Science Foundation of Guangdong Province [2018A0303130102, 2018A030313887]
  3. Guangdong Province Innovation Team Construction Program on Modern Agriculture Industrial technology system [2019KJ103]
  4. Science and Technology Planning Project of Guangdong Province [2017A050506044]
  5. Science and Technology Planning Project of Guangzhou City [201704030028]
  6. Key Program for Subject Research of Guangzhou University of Chinese Medicine [XK2019002]
  7. GDAS' Special Project of Science and Technology Development [2019GDASYL-0105002]
  8. High-level Leading Talent Introduction Program of GDAS [2016GDASRC-0102]

向作者/读者索取更多资源

Triple-negative breast cancer (TNBC) is an aggressive disease with worst prognosis than other subtypes of breast cancer. Owing to the lack of hormone receptors and HER2 expression on TNBC cells, patients do not have targeted therapy options available with other breast cancer subtypes. Extensive efforts have been made to identify novel therapeutics against TNBC. Interestingly, recent studies had shown that plant-derived natural products could modulate the autophagy and induce the breast cancer cells death. Seed ofBrucea javanicahas been used as an important traditional Chinese medicine against cancers. In the present study, the anti-breast cancer potential of ethanol crude extracts fromB. javanicaseed (BJE) was explored. Data demonstrated that BJE could inhibit the TNBC cell line MDA-MB-231 proliferation and induced apoptosis. In the cells exposed to BJE, protein expressions of UNC-51-like kinase-1 (ULK1) and Beclin-1 and the ratio of light chain 3 II/I (LC3 II/I) were reduced, while the expression of p62 was increased, indicating an inhibition on autophagy. Moreover, BJE promoted the phosphorylation of mammalian target of rapamycin (mTOR), phosphatidylinositol 3-kinase (PI3K), and Akt in MDA-MB-231. BJE also suppressed the MDA-MB-231 tumor growthin vivo. Coincide with the resultsin vitro, autophagy in the tumor tissue was weakened as indicated by decreased ratio of LC 3 II/I and Beclin-1 accompanied by enhanced phosphorylation of mTOR, which confirmed that autophagy restraint via the PI3K/Akt/mTOR signaling pathway contributes to the suppression by BJE. Notably, no noticeable toxicity in non-targeted organs was found, including small intestine, liver, and kidney. Taken together, this study revealed anti-breast cancer activity of BJE based on autophagy restraint, highlighting its clinical importance as a novel natural agent against TNBC.

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