Literature DB >> 18293085

Gene expression meta-analysis identifies chromosomal regions and candidate genes involved in breast cancer metastasis.

Mads Thomassen1, Qihua Tan, Torben A Kruse.   

Abstract

Breast cancer cells exhibit complex karyotypic alterations causing deregulation of numerous genes. Some of these genes are probably causal for cancer formation and local growth whereas others are causal for the various steps of metastasis. In a fraction of tumors deregulation of the same genes might be caused by epigenetic modulations, point mutations or the influence of other genes. We have investigated the relation of gene expression and chromosomal position, using eight datasets including more than 1200 breast tumors, to identify chromosomal regions and candidate genes possibly causal for breast cancer metastasis. By use of "Gene Set Enrichment Analysis" we have ranked chromosomal regions according to their relation to metastasis. Overrepresentation analysis identified regions with increased expression for chromosome 1q41-42, 8q24, 12q14, 16q22, 16q24, 17q12-21.2, 17q21-23, 17q25, 20q11, and 20q13 among metastasizing tumors and reduced gene expression at 1p31-21, 8p22-21, and 14q24. By analysis of genes with extremely imbalanced expression in these regions we identified DIRAS3 at 1p31, PSD3, LPL, EPHX2 at 8p21-22, and FOS at 14q24 as candidate metastasis suppressor genes. Potential metastasis promoting genes includes RECQL4 at 8q24, PRMT7 at 16q22, GINS2 at 16q24, and AURKA at 20q13.

Entities:  

Mesh:

Year:  2008        PMID: 18293085     DOI: 10.1007/s10549-008-9927-2

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  57 in total

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2.  Biomedical application of fuzzy association rules for identifying breast cancer biomarkers.

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3.  A long AAAG repeat allele in the 5' UTR of the ERR-γ gene is correlated with breast cancer predisposition and drives promoter activity in MCF-7 breast cancer cells.

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Journal:  Breast Cancer Res Treat       Date:  2010-12-10       Impact factor: 4.872

4.  Rothmund-Thomson Syndrome-like RECQL4 truncating mutations cause a haploinsufficient low bone mass phenotype in mice.

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Review 5.  EET signaling in cancer.

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Journal:  Am J Pathol       Date:  2011-02       Impact factor: 4.307

7.  Human RecQL4 helicase plays critical roles in prostate carcinogenesis.

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Journal:  Cancer Res       Date:  2010-11-02       Impact factor: 12.701

8.  The B-type lamin is required for somatic repression of testis-specific gene clusters.

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9.  Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast.

Authors:  Lesleyann Hawthorn; Jesse Luce; Leighton Stein; Jenniffer Rothschild
Journal:  BMC Cancer       Date:  2010-08-27       Impact factor: 4.430

10.  A resampling-based meta-analysis for detection of differential gene expression in breast cancer.

Authors:  Bala Gur-Dedeoglu; Ozlen Konu; Serkan Kir; Ahmet Rasit Ozturk; Betul Bozkurt; Gulusan Ergul; Isik G Yulug
Journal:  BMC Cancer       Date:  2008-12-30       Impact factor: 4.430

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