<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(12)</volume><submitter>Chen S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Ras homolog gene family member A (RhoA) is involved in Wnt-5a-induced migration of gastric and breast cancer cells. We investigated the roles of RhoA and Wnt-5a in ovarian carcinoma.&lt;h4>Methods&lt;/h4>RhoA and Wnt-5a mRNA and protein expression in normal fallopian tube epithelium, benign tumors, primary ovarian carcinomas, and metastatic omentum were quantified. RhoA or Wnt-5a was knocked down in OVCAR3 ovarian carcinoma cells using siRNAs and cell phenotype and expression of relevant molecules were assayed.&lt;h4>Results&lt;/h4>RhoA and Wnt-5a mRNA and protein expression were found to be significantly higher in metastatic omentum than in ovarian carcinomas, benign tumors, and normal fallopian tube epithelium (p &lt; 0.05), and positively associated with differentiation and FIGO sta</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>24187-99</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3876104</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The involvement of RhoA and Wnt-5a in the tumorigenesis and progression of ovarian epithelial carcinoma.</pubmed_title><pmcid>PMC3876104</pmcid><pubmed_authors>Zheng HC</pubmed_authors><pubmed_authors>Xiu YL</pubmed_authors><pubmed_authors>Zong ZH</pubmed_authors><pubmed_authors>Gou WF</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Takano Y</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>The involvement of RhoA and Wnt-5a in the tumorigenesis and progression of ovarian epithelial carcinoma.</name><description>&lt;h4>Background&lt;/h4>Ras homolog gene family member A (RhoA) is involved in Wnt-5a-induced migration of gastric and breast cancer cells. We investigated the roles of RhoA and Wnt-5a in ovarian carcinoma.&lt;h4>Methods&lt;/h4>RhoA and Wnt-5a mRNA and protein expression in normal fallopian tube epithelium, benign tumors, primary ovarian carcinomas, and metastatic omentum were quantified. RhoA or Wnt-5a was knocked down in OVCAR3 ovarian carcinoma cells using siRNAs and cell phenotype and expression of relevant molecules were assayed.&lt;h4>Results&lt;/h4>RhoA and Wnt-5a mRNA and protein expression were found to be significantly higher in metastatic omentum than in ovarian carcinomas, benign tumors, and normal fallopian tube epithelium (p &lt; 0.05), and positively associated with differentiation and FIGO sta</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Dec</publication><modification>2025-04-26T09:55:09.149Z</modification><creation>2019-03-27T01:19:09Z</creation></dates><accession>S-EPMC3876104</accession><cross_references><pubmed>24351810</pubmed><doi>10.3390/ijms141224187</doi></cross_references></HashMap>