COL4A1, negatively regulated by XPD and miR‑29a‑3p, promotes cell proliferation, migration, invasion and epithelial–mesenchymal transition in liver cancer cells
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[1] Second Affiliated Hospital of Nanchang University
Second Affiliated Hospital of Nanchang University
China
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[2] Department of Gastroenterology, The Second Clinical Medical College of Nanchang University, Nanchang 330006, Jiangxi, China
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- Localización: Clinical & translational oncology, ISSN 1699-048X, Vol. 23, Nº. 10, 2021, págs. 2078-2089
- Idioma: inglés
- Enlaces
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Resumen
Objective Collagen type IV alpha 1 (COL4A1) exerts tumor-promoting functions in several tumors. However, its role in liver cancer remains not fully understood. Hence, this study aims to investigate the role of COL4A1 in regulating liver cancer cell behaviors and to validate its upstream regulatory mechanism.
Methods Expression of xeroderma pigmentosum D (XPD) and COL4A1 was examined by qRT-PCR and western blot.
Cell proliferation, migration, and invasion were evaluated. The protein levels of N-cadherin, vimentin, and E-cadherin were determined by western blot to evaluate epithelial–mesenchymal transition (EMT). The interaction between miR-29a-3p and COL4A1 was analyzed by luciferase reporter assay.
Results COL4A1 overexpression significantly promoted cell proliferation, migration, invasion, and EMT in Hep3B cells.
In contrast, COL4A1 silencing yielded the opposite effects in HepG2 cells. Expression of COL4A1 was increased, whereas expression of XPD and miR-29a-3p was decreased in HCC tissues compared to controls. COL4A1 mRNA level was nega- tively correlated with expression of XPD and miR-29a-3p in HCC tissues. Furthermore, XPD silencing-mediated up-reg- ulation of COL4A1 expression was attenuated by miR-29a-3p mimic. Moreover, miR-29a-3p mimic inhibited Hep3B cell proliferation, migration, and invasion by directly targeting COL4A1.
Conclusion COL4A1 is negatively regulated by XPD-miR-29a-3p axis and promotes liver cancer progression in vitro.
