Literature DB >> 25592766

Evaluation of melanoma antigen (MAGE) gene expression in human cancers using The Cancer Genome Atlas.

Xiao Li1, Sarah C Hughes2, Rachel Wevrick3.   

Abstract

Melanoma antigen (MAGE) cancer-testis (CT) (or cancer-germline) genes are frequently over-expressed in cancer. However, the types of cancer in which the MAGE genes are over-expressed and the effect of over-expression on outcomes have been difficult to ascertain, and their relevance to progression is unclear. We queried transcriptomic and survival data from 26 cancer studies through the cBio Cancer Genomics Portal (www.cbioportal.org) to investigate dysregulation of 34 MAGE genes in cancer. MAGE genes are dysregulated in many cancers. Up to 44% of samples had over-expression of 22 Type 1 MAGE, which are not expressed in most normal tissues, or dysregulation of 12 Type 2 MAGE genes, which are expressed in normal tissues. Dysregulation of specific MAGE genes correlated with reduced overall survival in four cancer types (brain low grade gliomas, renal clear cell carcinomas, head and neck squamous cell carcinomas, and uterine corpus endometrioid carcinomas), with weaker correlations in four additional cancer types. This study demonstrates (1) the value of cancer-germline antigen expression profiling as a complement to mutation analysis for prognosis in cancer; (2) that over-expression of MAGE genes in a subset of cancers is associated with reduced survival; and (3) that patterns of MAGE expression could inform individualized treatment in cancer.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cancer-testis antigen; RNA sequencing; computational biology; individualized medicine; melanoma antigen; neoplasm RNA

Mesh:

Substances:

Year:  2014        PMID: 25592766     DOI: 10.1016/j.cancergen.2014.11.005

Source DB:  PubMed          Journal:  Cancer Genet


  7 in total

1.  Differential gene expression and network analysis in head and neck squamous cell carcinoma.

Authors:  Insan Habib; Farah Anjum; Taj Mohammad; Md Nayab Sulaimani; Alaa Shafie; Mazen Almehmadi; Dharmendra Kumar Yadav; Sukhwinder Singh Sohal; Md Imtaiyaz Hassan
Journal:  Mol Cell Biochem       Date:  2022-02-10       Impact factor: 3.396

2.  Pilot Study on MAGE-C2 as a Potential Biomarker for Triple-Negative Breast Cancer.

Authors:  Qian Zhao; Wen-Ting Xu; Tuluhong Shalieer
Journal:  Dis Markers       Date:  2016-10-24       Impact factor: 3.434

3.  Melanoma cells undergo aggressive coalescence in a 3D Matrigel model that is repressed by anti-CD44.

Authors:  Deborah Wessels; Daniel F Lusche; Edward Voss; Spencer Kuhl; Emma C Buchele; Michael R Klemme; Kanoe B Russell; Joseph Ambrose; Benjamin A Soll; Aaron Bossler; Mohammed Milhem; Charles Goldman; David R Soll
Journal:  PLoS One       Date:  2017-03-06       Impact factor: 3.240

4.  Suppressing Dazl modulates tumorigenicity and stemness in human glioblastoma cells.

Authors:  Fengyu Zhang; Ruilai Liu; Haishi Zhang; Cheng Liu; Chunfang Liu; Yuan Lu
Journal:  BMC Cancer       Date:  2020-07-18       Impact factor: 4.430

5.  The expression of the cancer testis antigen MAGE A4: A favorable prognostic biomarker in salivary gland carcinomas related to low tumor grading.

Authors:  Domenic Vital; Kristian Ikenberg; Holger Moch; Matthias Roessle; Gerhard F Huber
Journal:  Laryngoscope Investig Otolaryngol       Date:  2018-04-19

6.  Downregulation of Brain Enriched Type 2 MAGEs Is Associated With Immune Infiltration and Poor Prognosis in Glioma.

Authors:  Mohit Arora; Sarita Kumari; Jay Singh; Anita Chopra; Shyam S Chauhan
Journal:  Front Oncol       Date:  2020-12-23       Impact factor: 5.738

7.  DNA hypomethylation drives changes in MAGE-A gene expression resulting in alteration of proliferative status of cells.

Authors:  Ashley Colemon; Taylor M Harris; Saumya Ramanathan
Journal:  Genes Environ       Date:  2020-07-30
  7 in total

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