自噬
肝细胞癌
转移
癌症研究
血小板
转化生长因子
肝细胞癌
医学
癌症
生物
肿瘤科
内科学
细胞凋亡
生物化学
作者
Meng Lu,Xue Gong,Yumin Zhang,Ya-Wei Guo,Ying Zhu,Xiangbin Zeng,Jiahui Gao,Lu-Man Liu,Dan Shu,Rong Ma,Huifang Liang,Ruyi Zhang,Yun Xu,Bixiang Zhang,Yong‐Jie Lu,Zhangyin Ming
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2024-08-06
卷期号:600: 217161-217161
被引量:26
标识
DOI:10.1016/j.canlet.2024.217161
摘要
mice showed reduced TGF-β1 in primary tumors, which corresponded with decreased cancer cell EMT, autophagy, migration ability and tumor metastasis. Inhibition of autophagy via Atg5 knockdown in cancer cells negated EMT and metastasis induced by platelet-released TGF-β1. Clinically, higher platelet count correlated with increased TGF-β1, LC3 and N-cad expression in primary tumors of HCC patients, suggesting a link between platelets and HCC progression. Our study indicates that platelets promote cancer cell EMT in the primary tumor and HCC metastasis through TGF-β1-induced HCC cell autophagy via the AMPK/mTOR pathway. These findings offer novel insights into the role of platelets in HCC metastasis and the potential therapeutic targets for HCC metastasis.
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