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中华猕猴桃根通过 LAMB3 抑制肝癌细胞。

The root of Actinidia chinensis inhibits hepatocellular carcinomas cells through LAMB3.

机构信息

Zhongshan Hospital Institute of Clinical Science, Shanghai Institute of Clinical Bioinformatics; Zhongshan Hospital, Fudan University, Shanghai, 200032, China.

出版信息

Cell Biol Toxicol. 2018 Aug;34(4):321-332. doi: 10.1007/s10565-017-9416-7. Epub 2017 Nov 10.

Abstract

The root of Actinidia chinensis, as traditional Chinese medicine, has been shown to inhibit cell proliferation in numerous cancer cells. However, the mechanisms underlying its inhibitory activity remain unclear. Death rates of hepatocellular carcinoma (HCC) are increasing, but therapies for advanced HCC are not well developed. We choose the extract from root of Actinidia chinensis (ERAC) to treat the HCC cell lines in vitro, displaying distinct effects on cell proliferation, S-phase cell cycle arrest, and apoptosis. LAMB3, the gene encoding laminin subunit beta-3, plays a key role in the proliferation suppression and S-phase cell cycle arrest of HepG2 cells treated with ERAC. The downstream genes ITGA3, CCND2, and TP53 in LAMB3 pathway show the same response to ERAC as LAMB3. Thus, LAMB3 pathways, along with extracellular matrix-receptor interaction, pathways in cancer, and focal adhesion, are involved in the ERAC-induced suppressive response in HepG2.

摘要

猕猴桃根作为中药,已被证实能抑制多种癌细胞的增殖。但其抑制活性的机制尚不清楚。肝细胞癌(HCC)的死亡率正在上升,但晚期 HCC 的治疗方法并不完善。我们选择猕猴桃根提取物(ERAC)在体外治疗 HCC 细胞系,对细胞增殖、S 期细胞周期阻滞和细胞凋亡有明显影响。编码层粘连蛋白亚基β-3 的基因 LAMB3 在 ERAC 处理的 HepG2 细胞增殖抑制和 S 期细胞周期阻滞中起关键作用。LAMB3 通路中的下游基因 ITGA3、CCND2 和 TP53 对 ERAC 的反应与 LAMB3 相同。因此,LAMB3 通路以及细胞外基质-受体相互作用、癌症通路和黏着斑都参与了 ERAC 诱导的 HepG2 抑制反应。

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