首页> 美国卫生研究院文献>Oncology Letters >Reduced miR-433 expression is associated with advanced stages and early relapse of colorectal cancer and restored miR-433 expression suppresses the migration invasion and proliferation of tumor cells in vitro and in nude mice
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Reduced miR-433 expression is associated with advanced stages and early relapse of colorectal cancer and restored miR-433 expression suppresses the migration invasion and proliferation of tumor cells in vitro and in nude mice

机译:减少的miR-433表达与结直肠癌的晚期和早期复发有关恢复的miR-433表达抑制体外和裸鼠体内肿瘤细胞的迁移侵袭和增殖

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摘要

The expression of microRNA (miR-433) is altered in various types of human cancer. The present study analyzed the prognostic and biological value of miR-433 expression in colorectal cancer using reverse transcription-quantitative polymerase chain reaction in 125 colorectal tissue specimens (including a test cohort of 40 cases of paired colorectal cancer and adjacent normal mucosae and a confirmation cohort of 85 cases of stage I–III colorectal cancer). In vitro and nude mouse xenograft experiments were subsequently used to assess the effects of miR-433 expression on the regulation of colorectal cancer cell proliferation, adhesion, migration, and invasion. The data indicated that miR-433 expression was significantly downregulated in colorectal cancer tissues in the test and confirmation patient cohorts and that low miR-433 expression was associated with advanced tumor stage and early relapse. Furthermore, the restoration of miR-433 expression was able to significantly inhibit the proliferation of tumor cells by inducing G1-S cell cycle arrest, suppressing cyclinD1 and CDK4 expression, and markedly inhibited the migratory and invasive capacities of tumor cells in vitro. The restoration of miR-433 expression or liposome-based delivery of miR-433 mimics suppressed the growth of colorectal cancer cell xenografts in nude mice. In conclusion, miR-433 may be a putative tumor suppressor in colorectal cancer, and the detection of low miR-433 expression will be investigated in further studies as a putative biomarker for the detection of early relapse in patients with colorectal cancer.
机译:在各种类型的人类癌症中,microRNA(miR-433)的表达都发生了改变。本研究使用逆转录-定量聚合酶链反应分析了125例结直肠组织标本中的miR-433表达在大肠癌中的预后和生物学价值(包括40例结直肠癌和邻近正常粘膜配对患者的试验队列和一个确诊队列) 85例I–III期大肠癌病例)。随后使用体外和裸鼠异种移植实验评估miR-433表达对结肠直肠癌细胞增殖,粘附,迁移和侵袭的调节作用。数据表明,在测试和确认患者队列中,大肠癌组织中miR-433的表达明显下调,而miR-433的低表达与晚期肿瘤和早期复发相关。此外,miR-433表达的恢复能够通过诱导G1-S细胞周期停滞,抑制cyclinD1和CDK4表达来显着抑制肿瘤细胞的增殖,并显着抑制体外肿瘤细胞的迁移和侵袭能力。 miR-433表达的恢复或基于脂质体的miR-433模拟物的递送抑制了裸鼠中结直肠癌细胞异种移植的生长。总之,miR-433可能是结直肠癌的公认抑癌基因,miR-433低表达的检测将在进一步的研究中进行研究,作为检测结直肠癌患者早期复发的公认生物标志物。

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