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

Delic, Sabit and Thuy, Andreas and Schulze, Markus and Proescholdt, Martin A. and Dietrich, Peter and Bosserhoff, Anja-Katrin and Riemenschneider, Markus J. (2015) Systematic investigation of CMTM family genes suggests relevance to glioblastoma pathogenesis and CMTM1 and CMTM3 as priority targets. GENES CHROMOSOMES & CANCER, 54 (7). pp. 433-443. ISSN 1045-2257, 1098-2264

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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. (c) 2015 Wiley Periodicals, Inc.

Item Type: Article
Uncontrolled Keywords: TUMOR-SUPPRESSOR ACTIVITIES; GLIOMA INVASION; CELL CARCINOMA; IDENTIFICATION; METHYLATION; VALIDATION; ACTIVATION; APOPTOSIS; CLONING; GROWTH;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Abteilung für Neuropathologie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 08 Jul 2019 14:22
Last Modified: 08 Jul 2019 14:22
URI: https://pred.uni-regensburg.de/id/eprint/5285

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