Sunday, 14 November 2010

Transforming Properties of 8p11-12 Amplified Genes in Human Breast Cancer

Transforming Properties of 8p11-12 Amplified Genes in Human Breast Cancer — Cancer Res Skip to main page content

Home OnlineFirst Current Issue Past Issues Subscriptions Alerts Feedback AACR Publications AACR Home Search GO Advanced Search User Name Password Sign In AACR 102nd Annual Meeting 2011 Cancer Careers Transforming Properties of 8p11-12 Amplified Genes in Human Breast Cancer Zeng-Quan Yang1, Gang Liu1, Aliccia Bollig-Fischer1, Craig N. Giroux2, and Stephen P. Ethier1
Authors' Affiliations:1Breast Cancer Program and 2Systems and Computational Biology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan Corresponding Author:
Zeng-Quan Yang, Karmanos Cancer Institute, 4100 John R HWCRC 815, Detroit, MI 48201. Phone: 313-576-8339; Fax: 313-576-8029; E-mail: yangz{at}karmanos.org. Z.-Q. Yang and G. Liu contributed equally to this work.

Abstract Amplification of the 8p11-12 region has been found in about 15% of human breast cancers and is associated with poor prognosis. Earlier, we used genomic analysis of copy number and gene expression to perform a detailed analysis of the 8p11-12 amplicon to identify candidate oncogenes in breast cancer. We identified 21 candidate genes and provided evidence that three genes, namely, LSM-1, TC-1, and BAG4, have transforming properties when overexpressed. In the present study, we systematically investigated the transforming properties of 13 newly identified 8p11-12 candidate oncogenes in vitro. WHSC1L1, DDHD2, and ERLIN2 were most potently transforming oncogenes based on the number of altered phenotypes expressed by the cells. WHSC1L1 contains a PWWP-domain that is a methyl-lysine recognition motif involved in histone code modification and epigenetic regulation of gene expression. Knockdown of WHSC1L1 in 8p11-12–amplified breast cancer cells resulted in profound loss of growth and survival of these cells. Further, we identified several WHSC1L1 target genes, one of which is iroquois homeobox 3 gene (IRX3), a member of the Iroquois homeobox transcription factor family. Cancer Res; 70(21); 8487–97. ©2010 AACR.

Footnotes Note: Supplementary data for this article are available at Cancer Research Online (http://cancerres.aacrjournals.org/).

Received March 22, 2010. Revision received August 27, 2010. Accepted August 27, 2010. ©2010 American Association for Cancer Research. Add to CiteULikeCiteULike Add to ComploreComplore Add to ConnoteaConnotea Add to Del.icio.usDel.icio.us Add to DiggDigg Add to FacebookFacebook Add to RedditReddit Add to TechnoratiTechnorati Add to TwitterTwitter What's this?

« Previous | Next Article »Table of Contents This Article Published OnlineFirst October 12, 2010; doi: 10.1158/0008-5472.CAN-10-1013 Cancer Res November 1, 2010 70; 8487 » Abstract Full Text Full Text (PDF) Supplementary Data All Versions of this Article: 0008-5472.CAN-10-1013v1 70/21/8487 most recent Classifications Molecular and Cellular Pathobiology Services Email this article to a colleague Alert me when this article is cited Alert me if a correction is posted Similar articles in this journal Similar articles in PubMed Download to citation manager Citing Articles Load citing article information Citing articles via Scopus Google Scholar Articles by Yang, Z. Articles by Ethier, S. P. PubMed PubMed citation Articles by Yang, Z. Articles by Ethier, S. P. Social Bookmarking Add to CiteULikeCiteULike Add to ComploreComplore Add to ConnoteaConnotea Add to Del.icio.usDel.icio.us Add to DiggDigg Add to FacebookFacebook Add to RedditReddit Add to TechnoratiTechnorati Add to TwitterTwitter What's this?

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Online ISSN: 1538-7445 Print ISSN: 0008-5472

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