Cargando…
BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells
BIRC5/Survivin is known as a dual cellular functions protein that directly regulates both apoptosis and mitosis in embryonic cells during embryogenesis and in cancer cells during tumorigenesis and tumor metastasis. However, BIRC5 has seldom been demonstrated as a direct macroautophagy/autophagy regu...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469615/ https://www.ncbi.nlm.nih.gov/pubmed/31612776 http://dx.doi.org/10.1080/15548627.2019.1671643 |
_version_ | 1783578440136392704 |
---|---|
author | Lin, Tzu-Yu Chan, Hsiu-Han Chen, Shang-Hung Sarvagalla, Sailu Chen, Pai-Sheng Coumar, Mohane Selvaraj Cheng, Siao Muk Chang, Yung-Chieh Lin, Chun-Hui Leung, Euphemia Cheung, Chun Hei Antonio |
author_facet | Lin, Tzu-Yu Chan, Hsiu-Han Chen, Shang-Hung Sarvagalla, Sailu Chen, Pai-Sheng Coumar, Mohane Selvaraj Cheng, Siao Muk Chang, Yung-Chieh Lin, Chun-Hui Leung, Euphemia Cheung, Chun Hei Antonio |
author_sort | Lin, Tzu-Yu |
collection | PubMed |
description | BIRC5/Survivin is known as a dual cellular functions protein that directly regulates both apoptosis and mitosis in embryonic cells during embryogenesis and in cancer cells during tumorigenesis and tumor metastasis. However, BIRC5 has seldom been demonstrated as a direct macroautophagy/autophagy regulator in cells. ATG7 expression and ATG12–ATG5-ATG16L1 complex formation are crucial for the phagophore elongation during autophagy in mammalian cells. In this study, we observed that the protein expression levels of BIRC5 and ATG7 were inversely correlated, whereas the expression levels of BIRC5 and SQSTM1/p62 were positively correlated in normal breast tissues and tumor tissues. Mechanistically, we found that BIRC5 negatively modulates the protein stability of ATG7 and physically binds to the ATG12–ATG5 conjugate, preventing the formation of the ATG12–ATG5-ATG16L1 protein complex in human cancer (MDA-MB-231, MCF7, and A549) and mouse embryonic fibroblast (MEF) cells. We also observed a concurrent physical dissociation between BIRC5 and ATG12–ATG5 (but not CASP3/caspase-3) and upregulation of autophagy in MDA-MB-231 and A549 cells under serum-deprived conditions. Importantly, despite the fact that upregulation of autophagy is widely thought to promote DNA repair in cells under genotoxic stress, we found that BIRC5 maintains DNA integrity through autophagy negative-modulations in both human cancer and MEF cells under non-stressed conditions. In conclusion, our study reveals a novel role of BIRC5 in cancer cells as a direct regulator of autophagy. BIRC5 may act as a “bridging molecule”, which regulates the interplay between mitosis, apoptosis, and autophagy in embryonic and cancer cells. ABBREVIATIONS: ACTA1: actin; ATG: autophagy related; BIRC: baculoviral inhibitor of apoptosis repeat-containing; BAF: bafilomycin A(1); CQ: chloroquine; CASP3: caspase 3; HSPB1/Hsp27: heat shock protein family B (small) member 1/heat shock protein 27; IAPs: inhibitors of apoptosis proteins; IP: immunoprecipitation; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PLA: proximity ligation assay; SQSTM1/p62: sequestosome 1; siRNA: small interfering RNA |
format | Online Article Text |
id | pubmed-7469615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74696152020-09-15 BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells Lin, Tzu-Yu Chan, Hsiu-Han Chen, Shang-Hung Sarvagalla, Sailu Chen, Pai-Sheng Coumar, Mohane Selvaraj Cheng, Siao Muk Chang, Yung-Chieh Lin, Chun-Hui Leung, Euphemia Cheung, Chun Hei Antonio Autophagy Research Paper BIRC5/Survivin is known as a dual cellular functions protein that directly regulates both apoptosis and mitosis in embryonic cells during embryogenesis and in cancer cells during tumorigenesis and tumor metastasis. However, BIRC5 has seldom been demonstrated as a direct macroautophagy/autophagy regulator in cells. ATG7 expression and ATG12–ATG5-ATG16L1 complex formation are crucial for the phagophore elongation during autophagy in mammalian cells. In this study, we observed that the protein expression levels of BIRC5 and ATG7 were inversely correlated, whereas the expression levels of BIRC5 and SQSTM1/p62 were positively correlated in normal breast tissues and tumor tissues. Mechanistically, we found that BIRC5 negatively modulates the protein stability of ATG7 and physically binds to the ATG12–ATG5 conjugate, preventing the formation of the ATG12–ATG5-ATG16L1 protein complex in human cancer (MDA-MB-231, MCF7, and A549) and mouse embryonic fibroblast (MEF) cells. We also observed a concurrent physical dissociation between BIRC5 and ATG12–ATG5 (but not CASP3/caspase-3) and upregulation of autophagy in MDA-MB-231 and A549 cells under serum-deprived conditions. Importantly, despite the fact that upregulation of autophagy is widely thought to promote DNA repair in cells under genotoxic stress, we found that BIRC5 maintains DNA integrity through autophagy negative-modulations in both human cancer and MEF cells under non-stressed conditions. In conclusion, our study reveals a novel role of BIRC5 in cancer cells as a direct regulator of autophagy. BIRC5 may act as a “bridging molecule”, which regulates the interplay between mitosis, apoptosis, and autophagy in embryonic and cancer cells. ABBREVIATIONS: ACTA1: actin; ATG: autophagy related; BIRC: baculoviral inhibitor of apoptosis repeat-containing; BAF: bafilomycin A(1); CQ: chloroquine; CASP3: caspase 3; HSPB1/Hsp27: heat shock protein family B (small) member 1/heat shock protein 27; IAPs: inhibitors of apoptosis proteins; IP: immunoprecipitation; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; PLA: proximity ligation assay; SQSTM1/p62: sequestosome 1; siRNA: small interfering RNA Taylor & Francis 2019-10-15 /pmc/articles/PMC7469615/ /pubmed/31612776 http://dx.doi.org/10.1080/15548627.2019.1671643 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Lin, Tzu-Yu Chan, Hsiu-Han Chen, Shang-Hung Sarvagalla, Sailu Chen, Pai-Sheng Coumar, Mohane Selvaraj Cheng, Siao Muk Chang, Yung-Chieh Lin, Chun-Hui Leung, Euphemia Cheung, Chun Hei Antonio BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title | BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title_full | BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title_fullStr | BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title_full_unstemmed | BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title_short | BIRC5/Survivin is a novel ATG12–ATG5 conjugate interactor and an autophagy-induced DNA damage suppressor in human cancer and mouse embryonic fibroblast cells |
title_sort | birc5/survivin is a novel atg12–atg5 conjugate interactor and an autophagy-induced dna damage suppressor in human cancer and mouse embryonic fibroblast cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469615/ https://www.ncbi.nlm.nih.gov/pubmed/31612776 http://dx.doi.org/10.1080/15548627.2019.1671643 |
work_keys_str_mv | AT lintzuyu birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT chanhsiuhan birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT chenshanghung birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT sarvagallasailu birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT chenpaisheng birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT coumarmohaneselvaraj birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT chengsiaomuk birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT changyungchieh birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT linchunhui birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT leungeuphemia birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells AT cheungchunheiantonio birc5survivinisanovelatg12atg5conjugateinteractorandanautophagyinduceddnadamagesuppressorinhumancancerandmouseembryonicfibroblastcells |