<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(2)</volume><submitter>Matsuda R</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The aim of this study is to find a novel molecular target based on chromosomal alteration and array-based gene expression analyses in bladder cancer (BC). We investigated a cancer testis antigen, LY6K, which is located on chromosome 8q24.3.&lt;h4>Methods&lt;/h4>Five BC cell lines were subjected to high-resolution array-comparative genomic hybridisation with 244 000 probes. The expression levels of LY6K mRNA were evaluated in BC cell lines and clinical BC specimens by real-time reverse transcription-PCR. The cell lines were subjected to fluorescence in situ hybridisation of LY6K. Cell viability was evaluated by cell growth, wound healing, and matrigel invasion assays.&lt;h4>Results&lt;/h4>Typical gained loci (P&lt;0.0001) at 6p21.33-p21.32, 8q24.3, 9q34.13, 11q13.1-q14.1, 12q13.12-q13.1</pubmed_abstract><journal>British journal of cancer</journal><pagination>376-86</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3031884</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>LY6K is a novel molecular target in bladder cancer on basis of integrate genome-wide profiling.</pubmed_title><pmcid>PMC3031884</pmcid><pubmed_authors>Nakagawa M</pubmed_authors><pubmed_authors>Toki K</pubmed_authors><pubmed_authors>Tatarano S</pubmed_authors><pubmed_authors>Sugimoto T</pubmed_authors><pubmed_authors>Matsuda R</pubmed_authors><pubmed_authors>Kawakami K</pubmed_authors><pubmed_authors>Yoshino H</pubmed_authors><pubmed_authors>Kawahara K</pubmed_authors><pubmed_authors>Chiyomaru T</pubmed_authors><pubmed_authors>Nishiyama K</pubmed_authors><pubmed_authors>Enokida H</pubmed_authors><pubmed_authors>Kikkawa N</pubmed_authors><pubmed_authors>Seki N</pubmed_authors><pubmed_authors>Uchida Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>LY6K is a novel molecular target in bladder cancer on basis of integrate genome-wide profiling.</name><description>&lt;h4>Background&lt;/h4>The aim of this study is to find a novel molecular target based on chromosomal alteration and array-based gene expression analyses in bladder cancer (BC). We investigated a cancer testis antigen, LY6K, which is located on chromosome 8q24.3.&lt;h4>Methods&lt;/h4>Five BC cell lines were subjected to high-resolution array-comparative genomic hybridisation with 244 000 probes. The expression levels of LY6K mRNA were evaluated in BC cell lines and clinical BC specimens by real-time reverse transcription-PCR. The cell lines were subjected to fluorescence in situ hybridisation of LY6K. Cell viability was evaluated by cell growth, wound healing, and matrigel invasion assays.&lt;h4>Results&lt;/h4>Typical gained loci (P&lt;0.0001) at 6p21.33-p21.32, 8q24.3, 9q34.13, 11q13.1-q14.1, 12q13.12-q13.1</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jan</publication><modification>2025-04-03T22:18:30.409Z</modification><creation>2019-03-27T00:38:34Z</creation></dates><accession>S-EPMC3031884</accession><cross_references><pubmed>21063397</pubmed><doi>10.1038/sj.bjc.6605990</doi></cross_references></HashMap>