<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(28)</volume><submitter>Kumazaki M</submitter><pubmed_abstract>Tumor necrosis-factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a member of the TNF-superfamily that selectively induces apoptosis through death receptors (DRs) 4 and/or 5 in cancer cells. These receptors are expressed on the cancer cell surface, without affecting normal cells. Unfortunately, many clinical studies have shown that cancer cells acquire TRAIL-resistance and finally avoid TRAIL-induced apoptosis. The detailed mechanisms of this resistance are not well understood. In the current study, we established a TRAIL-resistant human colon cancer DLD-1 cell line to clarify the mechanisms of TRAIL-resistance and developed agents to cancel its machinery. Also, we found that cancer stem-like cells from breast epithelial proliferating MCF10A cells were also sensitive to TRAIL-induce</pubmed_abstract><journal>Oncotarget</journal><pagination>25828-42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4694869</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Understanding of tolerance in TRAIL-induced apoptosis and cancelation of its machinery by α-mangostin, a xanthone derivative.</pubmed_title><pmcid>PMC4694869</pmcid><pubmed_authors>Shinohara H</pubmed_authors><pubmed_authors>Ryo A</pubmed_authors><pubmed_authors>Taniguchi K</pubmed_authors><pubmed_authors>Akao Y</pubmed_authors><pubmed_authors>Nishi M</pubmed_authors><pubmed_authors>Kumazaki M</pubmed_authors><pubmed_authors>Ueda H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Understanding of tolerance in TRAIL-induced apoptosis and cancelation of its machinery by α-mangostin, a xanthone derivative.</name><description>Tumor necrosis-factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a member of the TNF-superfamily that selectively induces apoptosis through death receptors (DRs) 4 and/or 5 in cancer cells. These receptors are expressed on the cancer cell surface, without affecting normal cells. Unfortunately, many clinical studies have shown that cancer cells acquire TRAIL-resistance and finally avoid TRAIL-induced apoptosis. The detailed mechanisms of this resistance are not well understood. In the current study, we established a TRAIL-resistant human colon cancer DLD-1 cell line to clarify the mechanisms of TRAIL-resistance and developed agents to cancel its machinery. Also, we found that cancer stem-like cells from breast epithelial proliferating MCF10A cells were also sensitive to TRAIL-induce</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2025-04-04T03:42:20.689Z</modification><creation>2019-03-27T02:05:56Z</creation></dates><accession>S-EPMC4694869</accession><cross_references><pubmed>26304927</pubmed><doi>10.18632/oncotarget.4558</doi></cross_references></HashMap>