Suppr超能文献

在人类结直肠癌中,极低密度脂蛋白受体(VLDLR)表达降低与miR-200c呈负相关。

Decreased expression of VLDLR is inversely correlated with miR-200c in human colorectal cancer.

作者信息

Kim Bong-Kyu, Yoo Hye-In, Lee Ah-Reum, Choi Keonwoo, Yoon Sungjoo Kim

机构信息

Department of Medical Life Sciences, The Catholic University of Korea, Seoul, Korea.

出版信息

Mol Carcinog. 2017 Jun;56(6):1620-1629. doi: 10.1002/mc.22618. Epub 2017 Feb 8.

Abstract

Colorectal cancer (CRC) is one of the most common cancers and has a high rate of morbidity and mortality worldwide. Very-low-density-lipoprotein receptor (VLDLR), a member of the low-density-lipoprotein receptor (LDLR) superfamily, is a multifunctional receptor that regulates cellular signaling by binding numerous ligands. Several studies reported the altered expression of VLDLR and suggested that VLDLR may play a critical role in tumor development by affecting cell proliferation and metastasis. However, the function of VLDLR and regulation of its expression by miRNAs have not been investigated in CRC. In the present study, we investigated the expression of VLDLR in CRC patients and found it to be significantly decreased in tumors in comparison with paired adjacent non-tumor tissues. Moreover, VLDLR over-expression inhibited the proliferation and migration of CRC cells. We also found that VLDLR expression was negatively regulated by miR-200c in CRC cells and that their expression levels were inversely correlated in CRC patients. These data suggest that VLDLR down-regulation mediated by the increased expression of miR-200c may be involved in the development of CRC.

摘要

结直肠癌(CRC)是最常见的癌症之一,在全球范围内发病率和死亡率都很高。极低密度脂蛋白受体(VLDLR)是低密度脂蛋白受体(LDLR)超家族的成员之一,是一种多功能受体,通过结合多种配体来调节细胞信号传导。多项研究报道了VLDLR表达的改变,并表明VLDLR可能通过影响细胞增殖和转移在肿瘤发展中起关键作用。然而,VLDLR在结直肠癌中的功能及其表达受miRNA的调控尚未得到研究。在本研究中,我们调查了结直肠癌患者中VLDLR的表达,发现与配对的相邻非肿瘤组织相比,肿瘤中VLDLR的表达显著降低。此外,VLDLR的过表达抑制了结直肠癌细胞的增殖和迁移。我们还发现,在结直肠癌细胞中,VLDLR的表达受miR-200c的负调控,并且在结直肠癌患者中它们的表达水平呈负相关。这些数据表明,miR-200c表达增加介导的VLDLR下调可能参与了结直肠癌的发生发展。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验