4.7 Article

CHRNA5 Contributes to Hepatocellular Carcinoma Progression by Regulating YAP Activity

期刊

PHARMACEUTICS
卷 14, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics14020275

关键词

HCC; CHRNA5; metastasis; stemness property; sorafenib sensitivity

向作者/读者索取更多资源

In this study, the role of CHRNA5 in hepatocellular carcinoma (HCC) was investigated. Increased expression of CHRNA5 in HCC tissues was found to be positively correlated with tumor stage and worse survival in patients. Both in vitro and in vivo assays showed that CHRNA5 regulates HCC proliferation through the YAP pathway and promotes stemness through stemness-associated genes. Furthermore, CHRNA5 enhances HCC metastasis by regulating epithelial-mesenchymal transition (EMT)-associated genes. It was also observed that CHRNA5 affects the sensitivity of HCC to sorafenib treatment. These findings indicate that CHRNA5 plays a crucial role in HCC progression and drug resistance.
Hepatocellular carcinoma (HCC) is a major health concern worldwide. A better understanding of the mechanisms underlying the malignant phenotype is necessary for developing novel therapeutic strategies for HCC. Signaling pathways initiated by neurotransmitter receptors, such as alpha 5-nicotinic acetylcholine receptor (CHRNA5), have been reported to be implicated in tumor progression. However, the functional mechanism of CHRNA5 in HCC remains unclear. In this study, we explored the role of CHRNA5 in HCC and found that CHRNA5 expression was increased in human HCC tissues and positively correlated with the T stage (p < 0.05) and AJCC phase (p < 0.05). The KM plotter database showed that the high expression level of CHRNA5 was strongly associated with worse survival in HCC patients. Both in vitro and in vivo assays showed that CHRNA5 regulates the proliferation ability of HCC by regulating YAP activity. In addition, CHRNA5 promotes the stemness of HCC by regulating stemness-associated genes, such as Nanog, Sox2 and OCT4. Cell migration and invasion assays demonstrated that CHRNA5 significantly enhanced the metastasis of HCC by regulating epithelial-mesenchymal transition (EMT)-associated genes. Furthermore, we found that CHRNA5 regulates the sensitivity of sorafenib in HCC. Our findings suggest that CHRNA5 plays a key role in the progression and drug resistance of HCC, and targeting CHRNA5 may be a strategy for the treatment of HCC.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据