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中药有效成分紫堇灵通过泛素化介导 SRC-3 降解诱导 NSCLC 细胞凋亡

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

机构信息

School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Department of General Surgery, Xinhua Hospital Affiliated to Shanghai Jiaotong University, Shanghai, 200092, China.

出版信息

Cancer Lett. 2020 Nov 28;493:167-177. doi: 10.1016/j.canlet.2020.08.011. Epub 2020 Aug 20.

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.

摘要

非小细胞肺癌(NSCLC)占肺癌的 85%以上,发病率和死亡率都很高。越来越多的研究表明,中药(TCM)及其活性成分具有良好的抗肿瘤活性。然而,TCM 中的活性成分栀子苷(THB)在非小细胞肺癌中的抗肿瘤作用尚不清楚。在本研究中,据我们所知,这是首次基于我们之前的高通量筛选数据,报道其在非小细胞肺癌中抑制肿瘤活性的潜在机制。我们进一步证明,THB 通过诱导细胞凋亡而不是细胞周期阻滞,有效地抑制非小细胞肺癌细胞(A549 和 H460)的增殖。值得注意的是,THB 处理后 SRC-3 明显下调,这依赖于泛素-蛋白酶体介导的降解,从而通过体内和体外实验抑制 IGF-1R-PI3K-AKT 信号通路并促进细胞凋亡。总之,THB 通过泛素化抑制 SRC-3 介导的 IGF-1R-PI3K-AKT 信号通路,诱导细胞凋亡,从而发挥对非小细胞肺癌肿瘤生长的抑制作用,无论在体外还是体内,都具有最小的毒性。

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