<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(1)</volume><submitter>Xing X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>OPCML belongs to the IgLON family of Ig domain-containing GPI-anchored cell adhesion molecules and was recently found to be involved in carcinogenesis, while its role in gastric cancer remains unclear.&lt;h4>Methods&lt;/h4>We assessed expression and biological behavior of OPCML in gastric cancer.&lt;h4>Results&lt;/h4>OPCML expression was markedly reduced in tumor tissues and cancer cell lines. Decreased OPCML expression had a significant association with unfavorable tumor stage (p = 0.007) and grading (p &lt; 0.001). Furthermore, the results revealed that OPCML was an independent prognostic factor for overall survival in gastric cancer (p = 0.002). In addition, ectopic expression of OPCML in cancer cells significantly inhibited cell viability (p &lt; 0.01) and colony formation (p &lt; 0.001)</pubmed_abstract><journal>BMC cancer</journal><pagination>268</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5391589</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Down-regulated expression of OPCML predicts an unfavorable prognosis and promotes disease progression in human gastric cancer.</pubmed_title><pmcid>PMC5391589</pmcid><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Xing X</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Jiao J</pubmed_authors><pubmed_authors>Shi H</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Cai W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Down-regulated expression of OPCML predicts an unfavorable prognosis and promotes disease progression in human gastric cancer.</name><description>&lt;h4>Background&lt;/h4>OPCML belongs to the IgLON family of Ig domain-containing GPI-anchored cell adhesion molecules and was recently found to be involved in carcinogenesis, while its role in gastric cancer remains unclear.&lt;h4>Methods&lt;/h4>We assessed expression and biological behavior of OPCML in gastric cancer.&lt;h4>Results&lt;/h4>OPCML expression was markedly reduced in tumor tissues and cancer cell lines. Decreased OPCML expression had a significant association with unfavorable tumor stage (p = 0.007) and grading (p &lt; 0.001). Furthermore, the results revealed that OPCML was an independent prognostic factor for overall survival in gastric cancer (p = 0.002). In addition, ectopic expression of OPCML in cancer cells significantly inhibited cell viability (p &lt; 0.01) and colony formation (p &lt; 0.001)</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2026-07-09T10:35:26.144Z</modification><creation>2026-07-09T10:26:03.864Z</creation></dates><accession>S-EPMC5391589</accession><cross_references><pubmed>28407749</pubmed><doi>10.1186/s12885-017-3203-y</doi></cross_references></HashMap>