<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao YL</submitter><funding>NIEHS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>1923-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2375424</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>86(12)</volume><pubmed_abstract>Interaction between cell and extracellular matrix plays a crucial role in tumour invasion and metastasis. Using an immortalised human bronchial epithelial (BEP2D) cell model, the study here shows that expression of Betaig-h3 gene, which encodes a secreted adhesion molecule induced by transforming growth factor-beta, is markedly decreased in several independently generated, radiation-induced tumour cell lines (TL1-TL5) relative to parental BEP2D cells. Transfection of Betaig-h3 gene into tumour cells resulted in a significant reduction in tumour growth. While integrin receptor alpha5beta1 was overexpressed in tumour cells, its expression was corrected to the level found in control BEP2D cells after Betaig-h3 transfection. These data suggest that Betaig-h3 gene is involved in tumour progress</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>Overexpression of Betaig-h3 gene downregulates integrin alpha5beta1 and suppresses tumorigenicity in radiation-induced tumorigenic human bronchial epithelial cells.</pubmed_title><pmcid>PMC2375424</pmcid><funding_grant_id>P01 CA049062</funding_grant_id><funding_grant_id>ES07890</funding_grant_id><funding_grant_id>CA49062</funding_grant_id><pubmed_authors>Zhao YL</pubmed_authors><pubmed_authors>Hei TK</pubmed_authors><pubmed_authors>Piao CQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Overexpression of Betaig-h3 gene downregulates integrin alpha5beta1 and suppresses tumorigenicity in radiation-induced tumorigenic human bronchial epithelial cells.</name><description>Interaction between cell and extracellular matrix plays a crucial role in tumour invasion and metastasis. Using an immortalised human bronchial epithelial (BEP2D) cell model, the study here shows that expression of Betaig-h3 gene, which encodes a secreted adhesion molecule induced by transforming growth factor-beta, is markedly decreased in several independently generated, radiation-induced tumour cell lines (TL1-TL5) relative to parental BEP2D cells. Transfection of Betaig-h3 gene into tumour cells resulted in a significant reduction in tumour growth. While integrin receptor alpha5beta1 was overexpressed in tumour cells, its expression was corrected to the level found in control BEP2D cells after Betaig-h3 transfection. These data suggest that Betaig-h3 gene is involved in tumour progress</description><dates><release>2002-01-01T00:00:00Z</release><publication>2002 Jun</publication><modification>2025-04-25T23:07:34.928Z</modification><creation>2019-06-06T18:02:06Z</creation></dates><accession>S-EPMC2375424</accession><cross_references><pubmed>12085188</pubmed><doi>10.1038/sj.bjc.6600304</doi></cross_references></HashMap>