<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(52)</volume><submitter>Wang R</submitter><pubmed_abstract>Cancer stem cells (CSCs) are a key target for reducing tumor growth, metastasis, and recurrence. Redox status is a critical factor in the maintenance of CSCs, and the antioxidant enzyme Peroxiredoxin 2 (Prdx2) plays an important role in the development of colon cancer. Therefore, we investigated the contribution of Prdx2 to the maintenance of stemness of colon CSCs. Here, we used short-hairpin RNAs and a Prdx2-overexpression vector to determine the effects of Prdx2. We demonstrated that knockdown of Prdx2 reduced the self-renewal and sphere formation and resulted in increased 5-FU-induced apoptosis in human colon CSCs. Prdx2 overexpression induced reversion of the self-renewal and sphere formation. Furthermore, the effects of Prdx2 resulted in an altered expression of stemness associated w</pubmed_abstract><journal>Oncotarget</journal><pagination>86816-86828</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5349956</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Peroxiredoxin 2 is essential for maintaining cancer stem cell-like phenotype through activation of Hedgehog signaling pathway in colon cancer.</pubmed_title><pmcid>PMC5349956</pmcid><pubmed_authors>Lv Z</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Fu Z</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>You W</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Xiong Y</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Du K</pubmed_authors><pubmed_authors>Peng L</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Peroxiredoxin 2 is essential for maintaining cancer stem cell-like phenotype through activation of Hedgehog signaling pathway in colon cancer.</name><description>Cancer stem cells (CSCs) are a key target for reducing tumor growth, metastasis, and recurrence. Redox status is a critical factor in the maintenance of CSCs, and the antioxidant enzyme Peroxiredoxin 2 (Prdx2) plays an important role in the development of colon cancer. Therefore, we investigated the contribution of Prdx2 to the maintenance of stemness of colon CSCs. Here, we used short-hairpin RNAs and a Prdx2-overexpression vector to determine the effects of Prdx2. We demonstrated that knockdown of Prdx2 reduced the self-renewal and sphere formation and resulted in increased 5-FU-induced apoptosis in human colon CSCs. Prdx2 overexpression induced reversion of the self-renewal and sphere formation. Furthermore, the effects of Prdx2 resulted in an altered expression of stemness associated w</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2025-04-26T19:21:12.283Z</modification><creation>2020-11-07T11:32:23Z</creation></dates><accession>S-EPMC5349956</accession><cross_references><pubmed>27894099</pubmed><doi>10.18632/oncotarget.13559</doi></cross_references></HashMap>