肝细胞癌
表观遗传学
上皮-间质转换
DNA甲基化
转移
肿瘤进展
调节器
小RNA
癌症研究
生物
遗传学
癌症
基因表达
基因
作者
Anning Zuo,Jinyu Li,Siyuan Weng,Hui Xu,Yuyuan Zhang,Libo Wang,Zhe Xing,Peng Luo,Quan Cheng,Jing Li,Xinwei Han,Zaoqu Liu
标识
DOI:10.1021/acs.jproteome.4c00036
摘要
Epigenetic dysregulation drives aberrant transcriptional programs playing a critical role in hepatocellular carcinoma (HCC), which may provide novel insights into the heterogeneity of HCC. This study performed an integrated exploration on the epigenetic dysregulation of miRNA and methylation. We discovered and validated three patterns endowed with gene-related transcriptional traits and clinical outcomes. Specially, a stemness/epithelial–mesenchymal transition (EMT) subtype was featured by immune exhaustion and the worst prognosis. Besides, MMP12, a characteristic gene, was highly expressed in the stemness/EMT subtype, which was verified as a pivotal regulator linked to the unfavorable prognosis and further proven to promote tumor proliferation, invasion, and metastasis in vitro experiments. Proteomic analysis by mass spectrometry sequencing also indicated that the overexpression of MMP12 was significantly associated with cell proliferation and adhesion. Taken together, this study unveils innovative insights into epigenetic dysregulation and identifies a stemness/EMT subtype-specific gene, MMP12, correlated with the progression and prognosis of HCC.
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