<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shahriari Felordi M</submitter><funding>Royan Institute</funding><funding>Bahar Tashkhis Teb Co</funding><pagination>2572-2582</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10468655</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(17)</volume><pubmed_abstract>Anti-cancer properties of (-)-epigallocatechin-3-gallate (EGCG) are mediated via apoptosis induction, as well as inhibition of cell proliferation and histone deacetylase. Accumulation of stabilized cellular FLICE-inhibitory protein (c-FLIP)/Ku70 complex in the cytoplasm inhibits apoptosis through interruption of extrinsic apoptosis pathway. In this study, we evaluated the anti-cancer role of EGCG in gastric cancer (GC) cells through dissociation of c-FLIP/Ku70 complex. MKN-45 cells were treated with EGCG or its antagonist MG149 for 24 h. Apoptosis was evaluated by flow cytometry and quantitative RT-PCR. Protein expression of c-FLIP and Ku70 was analysed using western blot and immunofluorescence. Dissociation of c-FLIP/Ku70 complex as well as Ku70 translocation were studied by sub-cellular </pubmed_abstract><journal>Journal of cellular and molecular medicine</journal><pubmed_title>(-)-Epigallocatechin-3-gallate induced apoptosis by dissociation of c-FLIP/Ku70 complex in gastric cancer cells.</pubmed_title><pmcid>PMC10468655</pmcid><funding_grant_id>R.98005</funding_grant_id><funding_grant_id>R1398-0335</funding_grant_id><funding_grant_id>R1398‐0335</funding_grant_id><pubmed_authors>Shahriari Felordi M</pubmed_authors><pubmed_authors>Alikhani M</pubmed_authors><pubmed_authors>Piryaei A</pubmed_authors><pubmed_authors>Ebrahimi M</pubmed_authors><pubmed_authors>Aboulkheyr Es H</pubmed_authors><pubmed_authors>Farzaneh Z</pubmed_authors><pubmed_authors>Alipour Choshali M</pubmed_authors><pubmed_authors>Vosough M</pubmed_authors><pubmed_authors>Najimi M</pubmed_authors></additional><is_claimable>false</is_claimable><name>(-)-Epigallocatechin-3-gallate induced apoptosis by dissociation of c-FLIP/Ku70 complex in gastric cancer cells.</name><description>Anti-cancer properties of (-)-epigallocatechin-3-gallate (EGCG) are mediated via apoptosis induction, as well as inhibition of cell proliferation and histone deacetylase. Accumulation of stabilized cellular FLICE-inhibitory protein (c-FLIP)/Ku70 complex in the cytoplasm inhibits apoptosis through interruption of extrinsic apoptosis pathway. In this study, we evaluated the anti-cancer role of EGCG in gastric cancer (GC) cells through dissociation of c-FLIP/Ku70 complex. MKN-45 cells were treated with EGCG or its antagonist MG149 for 24 h. Apoptosis was evaluated by flow cytometry and quantitative RT-PCR. Protein expression of c-FLIP and Ku70 was analysed using western blot and immunofluorescence. Dissociation of c-FLIP/Ku70 complex as well as Ku70 translocation were studied by sub-cellular </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-25T20:22:19.981Z</modification><creation>2025-04-06T08:18:26.779Z</creation></dates><accession>S-EPMC10468655</accession><cross_references><pubmed>37537749</pubmed><doi>10.1111/jcmm.17873</doi></cross_references></HashMap>