Cell & Bioscience | |
Huaier polysaccharides suppress triple-negative breast cancer metastasis and epithelial-mesenchymal transition by inducing autophagic degradation of Snail | |
Peng Tang1  Jun Jiang1  Yuzhao Yan1  Lingjuan Zeng1  Yuan Tian1  Qinwen Pan1  Zhen Zeng1  Jin Wu1  Linxi Zhou1  Ying Hu1  Zhaoyu Wang1  Ziwei Wu1  Wei Liu1  Minghao Wang1  | |
[1] Breast Disease Center, Southwest Hospital, Army Medical University; | |
关键词: Triple-negative breast cancer; Metastasis; Invasion; Huaier; In vitro; In vivo; | |
DOI : 10.1186/s13578-021-00682-6 | |
来源: DOAJ |
【 摘 要 】
Abstract Background Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer, and the targeted therapies are lacking for this type of cancer. We previously demonstrated that Huaier effectively improve 5-year OS and DFS in stage III TNBC patients, and the polysaccharides of Huaier (PS-T) have been identified as the major components of Huaier. However, the mechanisms of anti-tumor action of PS-T is unclear. This study aimed to investigate the effect of PS-T on TNBC cell invasion and migration. Results This study showed that PS-T inhibited cell invasion and migration both in vitro and in vivo by inducing autophagy to suppress epithelial-mesenchymal transition (EMT). Autophagy inhibitor LY294002 or knockdown of ATG5 suppressed the inhibitory effects of PS-T. In addition, as a key transcription factor controlling EMT initiation, Snail was found to be degraded by PS-T induced autophagy. In addition, overexpression of Snail reversed the inhibitory effects of PS-T. Furthermore, it was confirmed that the expression of Snail was inversely correlated with LC3 and associated with poor prognosis using immunohistochemistry and TCGA database analysis, respectively. Conclusions This study demonstrated that PS-T could inhibit EMT in breast cancer cells by inducing autophagy to degrade Snail protein, thus improving the prognosis of TNBC, offering potential treatment alternatives for TNBC patients.
【 授权许可】
Unknown