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MicroRNA-29c-3p acts as a tumor suppressor gene and inhibits tumor progression in hepatocellular carcinoma by targeting TRIM31

机译:MicroRNA-29C-3P用作肿瘤抑制基因,通过靶向TRIM31抑制肝细胞癌中的肿瘤进展

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摘要

Aberrant expression of microRNAs (miRNAs) has been widely reported in many malignant tumors, and dysregulated miRNAs play an important role in the malignant progression of tumors. It has been reported that miR-29c-3p expression is dysregulated in tumors and promotes the development of tumors, especially in hepatocellular carcinoma (HCC). However, the specific mechanism of miR-29c-3p in HCC is not clear. The present study demonstrated that miR-29c-3p was expressed at low levels in HCC patients and cell lines and that its decreased expression was closely related to poor prognosis of HCC patients. Overexpression of miR-29c-3p could significantly inhibit the proliferation and migration of HCC cells in vitro and suppress the HCC tumor growth in vivo. The luciferase reporter assay demonstrated that miR-29c-3p directly bound to tripartite motif containing 31 (TRIM31) and suppressed TRIM31 expression. Finally, upregulation of TRIM31 could partially abolish the tumor suppressing roles of miR-29c-3p in HCC. Overall, miR-29c-3p, as a tumor suppressor gene, was revealed to inhibit the malignant progression of HCC by reducing the expression of TRIM31 and may be used as a potential therapeutic target for the precise treatment of HCC.
机译:在许多恶性肿瘤中被广泛报道了MicroRNA(miRNA)的异常表达,并且失去了失去的miRNA在肿瘤的恶性进展中发挥着重要作用。据报道,MiR-29C-3P表达在肿瘤中讨论并促进肿瘤的发育,特别是在肝细胞癌(HCC)中。然而,HCC中MIR-29C-3P的特定机制尚不清楚。本研究表明,MIR-29C-3P在HCC患者和细胞系中的低水平表达,其表达下降与HCC患者的预后不良密切相关。 miR-29c-3p的过度表达可以显着抑制HCC细胞在体外的增殖和迁移,并抑制体内HCC肿瘤生长。荧光素酶报告器测定证明了MiR-29C-3P直接与含有31(TRIM31)的三方基序和抑制的TRIM31表达的结合。最后,Trim31的上调可以部分地取消HCC中miR-29c-3p的肿瘤抑制作用。总体而言,作为肿瘤抑制基因的MiR-29C-3P被揭示以通过减少Trim31的表达来抑制HCC的恶性进展,并且可以用作HCC精确处理的潜在治疗靶标。

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