<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tan S</submitter><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Hunan Province</funding><pagination>42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6580496</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24</volume><pubmed_abstract>Human bronchial epithelium (HBE)-Dp71 anti-sense(AS)cells with stably transfected Dp71 siRNA plasmids were prepared for further exploration of Dp71 biological traits in cells other than PC12. HBE-Dp71AS cells displayed increased DNA damage induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>. Apoptosis of HBE-Dp71AS cells induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> was increased via enhancing caspase 3, caspase 8 and caspase 9. HBE-Dp71AS cells also displayed decreased proliferation and clonogenic formation. RAD51 was proved to be a new binding partner of Dp71 by co-immunoprecipitation (Ip) and immunofluorescence. Reduced RAD51 mRNA and protein levels were observed in HBE-Dp71AS cells. Decreased lamin B1, focal adhesion kinase (FAK), phosphorylated focal adhesion kinase (p-FAK) and phosphorylated protein kinas</pubmed_abstract><journal>Cellular &amp; molecular biology letters</journal><pubmed_title>Dp71 depleted HBE cells displayed increased DNA damage and apoptosis induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>.</pubmed_title><pmcid>PMC6580496</pmcid><funding_grant_id>81870071</funding_grant_id><funding_grant_id>06C0410</funding_grant_id><pubmed_authors>Zhao S</pubmed_authors><pubmed_authors>Xiao L</pubmed_authors><pubmed_authors>Xie J</pubmed_authors><pubmed_authors>Xiao X</pubmed_authors><pubmed_authors>Tan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dp71 depleted HBE cells displayed increased DNA damage and apoptosis induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>.</name><description>Human bronchial epithelium (HBE)-Dp71 anti-sense(AS)cells with stably transfected Dp71 siRNA plasmids were prepared for further exploration of Dp71 biological traits in cells other than PC12. HBE-Dp71AS cells displayed increased DNA damage induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>. Apoptosis of HBE-Dp71AS cells induced by H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> was increased via enhancing caspase 3, caspase 8 and caspase 9. HBE-Dp71AS cells also displayed decreased proliferation and clonogenic formation. RAD51 was proved to be a new binding partner of Dp71 by co-immunoprecipitation (Ip) and immunofluorescence. Reduced RAD51 mRNA and protein levels were observed in HBE-Dp71AS cells. Decreased lamin B1, focal adhesion kinase (FAK), phosphorylated focal adhesion kinase (p-FAK) and phosphorylated protein kinas</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-04-08T05:24:40.042Z</modification><creation>2019-07-24T07:20:31Z</creation></dates><accession>S-EPMC6580496</accession><cross_references><pubmed>31236120</pubmed><doi>10.1186/s11658-019-0169-6</doi></cross_references></HashMap>