<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Armartmuntree N</submitter><funding>Khon Kaen University</funding><pagination>637-644</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5701798</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14</volume><pubmed_abstract>Early B cell factor 1 (EBF1) is a transcription factor involved in the differentiation of several stem cell lineages and it is a negative regulator of estrogen receptors. EBF1 is down-regulated in many tumors, and is believed to play suppressive roles in cancer promotion and progression. However, the functional roles of EBF1 in carcinogenesis are unclear. Liver fluke-infection-associated cholangiocarcinoma (CCA) is an oxidative stress-driven cancer of bile duct epithelium. In this study, we investigated EBF1 expression in tissues from CCA patients, CCA cell lines (KKU-213, KKU-214 and KKU-156), cholangiocyte (MMNK1) and its oxidative stress-resistant (ox-MMNK1-L) cell lines. The formation of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) was used as an oxidative stress marker. Our results r</pubmed_abstract><journal>Redox biology</journal><pubmed_title>Prolonged oxidative stress down-regulates Early B cell factor 1 with inhibition of its tumor suppressive function against cholangiocarcinoma genesis.</pubmed_title><pmcid>PMC5701798</pmcid><funding_grant_id>IN58140</funding_grant_id><funding_grant_id>I57327</funding_grant_id><funding_grant_id>LFCRC 003/2556</funding_grant_id><funding_grant_id>RSA5980031</funding_grant_id><funding_grant_id>591001</funding_grant_id><pubmed_authors>Yongvanit P</pubmed_authors><pubmed_authors>Pinlaor S</pubmed_authors><pubmed_authors>Pairojkul C</pubmed_authors><pubmed_authors>Loilome W</pubmed_authors><pubmed_authors>Murata M</pubmed_authors><pubmed_authors>Sakonsinsiri C</pubmed_authors><pubmed_authors>Thanan R</pubmed_authors><pubmed_authors>Techasen A</pubmed_authors><pubmed_authors>Namwat N</pubmed_authors><pubmed_authors>Armartmuntree N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prolonged oxidative stress down-regulates Early B cell factor 1 with inhibition of its tumor suppressive function against cholangiocarcinoma genesis.</name><description>Early B cell factor 1 (EBF1) is a transcription factor involved in the differentiation of several stem cell lineages and it is a negative regulator of estrogen receptors. EBF1 is down-regulated in many tumors, and is believed to play suppressive roles in cancer promotion and progression. However, the functional roles of EBF1 in carcinogenesis are unclear. Liver fluke-infection-associated cholangiocarcinoma (CCA) is an oxidative stress-driven cancer of bile duct epithelium. In this study, we investigated EBF1 expression in tissues from CCA patients, CCA cell lines (KKU-213, KKU-214 and KKU-156), cholangiocyte (MMNK1) and its oxidative stress-resistant (ox-MMNK1-L) cell lines. The formation of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) was used as an oxidative stress marker. Our results r</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2025-04-18T19:46:16.875Z</modification><creation>2019-03-27T03:02:56Z</creation></dates><accession>S-EPMC5701798</accession><cross_references><pubmed>29169115</pubmed><doi>10.1016/j.redox.2017.11.011</doi></cross_references></HashMap>