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对CMTM家族基因的系统研究表明其与胶质母细胞瘤发病机制相关,且CMTM1和CMTM3为优先研究靶点。

Systematic investigation of CMTM family genes suggests relevance to glioblastoma pathogenesis and CMTM1 and CMTM3 as priority targets.

作者信息

Delic Sabit, Thuy Andreas, Schulze Markus, Proescholdt Martin A, Dietrich Peter, Bosserhoff Anja-Katrin, Riemenschneider Markus J

机构信息

Department of Neuropathology, Regensburg University Hospital, Regensburg, Germany.

Department of Neurosurgery and, Regensburg University Hospital, Regensburg, Germany.

出版信息

Genes Chromosomes Cancer. 2015 Jul;54(7):433-43. doi: 10.1002/gcc.22255. Epub 2015 Apr 30.

Abstract

The novel CKLF-like Marvel Transmembrane Domain-containing gene family (CMTM) consists of 8 members (CMTM1-8). As little is known about the oncogenic impact of these genes, we aimed to systematically investigate the relevance of CMTMs to glioblastoma pathogenesis. We performed mRNA expression analyses and survival correlations in glioblastoma patients. Moreover, we analyzed the impact of RNAi-based silencing and overexpression of CMTM family genes on tumor cell proliferation and invasion in vitro. CMTMs appeared to be widely regulated in the group of glioblastomas relative to non-neoplastic brain (NB) tissue (significant upregulation for CMTM2, 3, and 6 and significant downregulation for CMTM 4 and 8). For CMTM1, 5 and 7, we found aberrant expression levels in individual tumors. Functionally, CMTM1, 3, and 7 promoted tumor cell invasion, while CMTM1 additionally enhanced cell proliferation. In a large clinically annotated dataset, higher CMTM1 and 3 expression was significantly correlated with shorter overall survival. Our data thus suggest CMTM1 and 3 as priority targets in glioblastomas. Using a human phosphokinase protein expression profiling assay, we can provide first insights into signalling of these two genes that might be conveyed by growth factor receptor, Src family kinase and WNT activation.

摘要

新型含CKLF样MARVEL跨膜结构域基因家族(CMTM)由8个成员(CMTM1 - 8)组成。由于对这些基因的致癌作用了解甚少,我们旨在系统研究CMTM与胶质母细胞瘤发病机制的相关性。我们对胶质母细胞瘤患者进行了mRNA表达分析和生存相关性研究。此外,我们分析了基于RNA干扰的CMTM家族基因沉默和过表达对体外肿瘤细胞增殖和侵袭的影响。相对于非肿瘤性脑(NB)组织,CMTM在胶质母细胞瘤组中似乎受到广泛调控(CMTM2、3和6显著上调,CMTM4和8显著下调)。对于CMTM1、5和7,我们在个别肿瘤中发现了异常表达水平。在功能上,CMTM1、3和7促进肿瘤细胞侵袭,而CMTM1还增强细胞增殖。在一个大型临床注释数据集中,较高的CMTM1和3表达与较短的总生存期显著相关。因此,我们的数据表明CMTM1和3是胶质母细胞瘤的优先靶点。通过人类磷酸激酶蛋白表达谱分析,我们可以初步了解这两个基因可能通过生长因子受体、Src家族激酶和WNT激活传递的信号。

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