1. Academic Validation
  2. Thevebioside, the active ingredient of traditional Chinese medicine, promotes ubiquitin-mediated SRC-3 degradation to induce NSCLC cells apoptosis

Thevebioside, the active ingredient of traditional Chinese medicine, promotes ubiquitin-mediated SRC-3 degradation to induce NSCLC cells apoptosis

  • Cancer Lett. 2020 Nov 28:493:167-177. doi: 10.1016/j.canlet.2020.08.011.
Chao Yao 1 Lin Su 1 Fei Zhang 2 Xiaowen Zhu 1 Yangzhuangzhuang Zhu 1 Luyao Wei 1 Xiaoning Jiao 1 Yifei Hou 1 Xiao Chen 1 Wantao Wang 1 Jie Wang 1 Xiandan Zhu 3 Chunpu Zou 4 Shiguo Zhu 5 Zihang Xu 6
Affiliations

Affiliations

  • 1 School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
  • 2 Department of General Surgery, Xinhua Hospital Affiliated to Shanghai Jiaotong University, Shanghai, 200092, China.
  • 3 Experimental Center for Science and Technology, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
  • 4 School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. Electronic address: [email protected].
  • 5 School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. Electronic address: [email protected].
  • 6 School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. Electronic address: [email protected].
Abstract

Non-small cell lung Cancer (NSCLC) accounts for more than 85% of lung Cancer with high incidence and mortality. Accumulating studies have shown that traditional Chinese medicine (TCM) and its active ingredients have good anti-tumor activity. However, the anti-tumor effect of Thevebioside (THB), an active ingredient from TCM, is still unknown in NSCLC. In this study, to our best knowledge, it was the first time to report the underlying mechanism of its tumor-suppressive activity in NSCLC based on our previous high-throughput screening data. We further demonstrated that THB effectively inhibited the proliferation of NSCLC cells (A549 and H460) by inducing cellular Apoptosis rather than cell cycle arrest. Notably, it was demonstrated that SRC-3 was significantly down-regulated after THB treatment dependent on ubiquitin-proteasome-mediated degradation, which subsequently inhibited the IGF-1R-PI3K-AKT signaling pathway and promoted Apoptosis via both in vivo and in vitro experiments. Collectively, THB exerted inhibitory effect on tumor growth of NSCLC through inhibiting SRC-3 mediated IGF-1R-PI3K-AKT signaling by ubiquitination to induce cellular Apoptosis with minimal toxicity no matter in vitro or vivo.

Keywords

Non-small cell lung cancer; Steroid receptor coactivator-3; TCM; THB; Ubiquitin-proteasome pathway.

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