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血管生成素相关蛋白 4 转录本 3 促进肝癌细胞的增殖、侵袭和迁移,并抑制细胞凋亡。

Angiopoietin-Related Protein 4-Transcript 3 Increases the Proliferation, Invasion, and Migration of Hepatocellular Carcinoma Cells and Inhibits Apoptosis.

机构信息

Department of Oncology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

DNA Cell Biol. 2024 Apr;43(4):175-184. doi: 10.1089/dna.2023.0392. Epub 2024 Mar 11.

Abstract

To investigate the functional differences of angiopoietin-related protein 4 () transcripts in hepatocellular carcinoma (HCC) cells. By transfecting -Transcript 1 and -Transcript 3 overexpression vectors into HepG2 and Huh7 cell lines with knockdown, the effects of overexpression of two transcripts on cell viability, invasion, migration, and apoptosis were analyzed. The expression of two transcripts was compared in human liver cancer tissue, and their effects on tumor development were validated experiments in mice. Compared with control, the overexpression of -Transcript 1 had no significant effect on viability, invasion, healing, and apoptosis of HepG2 and Huh7 cells. However, these two cell lines overexpressing -Transcript 3 showed remarkably enhanced cell viability, invasive and healing ability, and decreased apoptosis ability. Furthermore, the mRNA level of -Transcript 3 was significantly increased in human HCC tissues and promoted tumor growth compared with Transcript 1. Different transcripts of gene have distinct effects on HCC. The abnormally elevated Transcript 3 with the specific ability of promoting HCC proliferation, infiltration, and migration is expected to become a new biological marker and more precise intervention target for HCC.

摘要

为了研究血管生成素相关蛋白 4 () 转录本在肝细胞癌 (HCC) 细胞中的功能差异。通过转染 -Transcript 1 和 -Transcript 3 过表达载体到下调的 HepG2 和 Huh7 细胞系中,分析了两种转录本过表达对细胞活力、侵袭、迁移和凋亡的影响。比较了两种转录本在人肝癌组织中的表达,并在小鼠中验证了它们对肿瘤发展的影响实验。与对照组相比,-Transcript 1 的过表达对 HepG2 和 Huh7 细胞的活力、侵袭、愈合和凋亡没有显著影响。然而,这两种过表达 -Transcript 3 的细胞系表现出显著增强的细胞活力、侵袭和愈合能力,以及降低的凋亡能力。此外,与 Transcript 1 相比,-Transcript 3 的 mRNA 水平在人 HCC 组织中显著增加,并促进肿瘤生长。基因的不同转录本对 HCC 有不同的影响。具有促进 HCC 增殖、浸润和迁移特定能力的异常升高的 Transcript 3 有望成为 HCC 的新生物标志物和更精确的干预靶点。

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