ETV4 facilitates angiogenesis in hepatocellular carcinoma by upregulating MMP14 expression

血管生成 癌症研究 转移 基因敲除 癌变 肝细胞癌 肿瘤进展 生物 新生血管 癌症 医学 细胞培养 遗传学
作者
Hongmeng Su,Shihui Shu,Wenyi Tang,Chuanchao Zheng,Luyu Zhao,Hong Fan
出处
期刊:Biochemical and Biophysical Research Communications [Elsevier]
卷期号:: 149137-149137
标识
DOI:10.1016/j.bbrc.2023.149137
摘要

Abnormal vascularization plays a crucial role in cell proliferation, tumor invasion and metastasis of hepatocellular carcinoma (HCC). It has been reported that ETV4 functions as an oncogenic gene in driving the carcinogenesis and progression, and promoting invasion and metastasis of HCC. However, the function of ETV4 on angiogenesis in HCC remains unclear. In the current study, immunohistochemistry showed that knockdown of ETV4 reduced angiogenesis in HCC xenograft tumor tissues. In vitro, tube formation assay verified that ETV4 expression promoted angiogenesis through simulating the angiogenic environment in HCC cells. Transcriptome sequencing indicated that MMP14 was one of the differentially expressed genes enriched in angiogenesis process. Subsequently, it was confirmed that MMP14 was regulated by ETV4 at the transcription level in HCC cells, clinical tissue samples and online databases. Further, we demonstrated that MMP14 induced angiogenesis in ETV4-mediated HCC microenvironment. Collectively, this research further reveals the biological mechanism of ETV4 in promoting the migration and invasion of HCC, and provides novel mechanistic insights and strategic guidance for anti-angiogenic therapy in HCC.
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