Cargando…
c-FLIP is a target of the E3 ligase deltex1 in gastric cancer
The ubiquitin E3 ligase DELTEX1 (DTX1) is specifically downregulated in gastric cancer tissues, and expression of DTX1 is linked to better prognoses and survival in gastric cancer. Cellular FLICE inhibitory protein (c-FLIP) is known for its pivotal role in the resistance of cancer cells to death rec...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833402/ https://www.ncbi.nlm.nih.gov/pubmed/29374180 http://dx.doi.org/10.1038/s41419-017-0165-6 |
_version_ | 1783303479798792192 |
---|---|
author | Hsu, Tzu-Sheng Mo, Shu-Ting Hsu, Ping-Ning Lai, Ming-Zong |
author_facet | Hsu, Tzu-Sheng Mo, Shu-Ting Hsu, Ping-Ning Lai, Ming-Zong |
author_sort | Hsu, Tzu-Sheng |
collection | PubMed |
description | The ubiquitin E3 ligase DELTEX1 (DTX1) is specifically downregulated in gastric cancer tissues, and expression of DTX1 is linked to better prognoses and survival in gastric cancer. Cellular FLICE inhibitory protein (c-FLIP) is known for its pivotal role in the resistance of cancer cells to death receptor-induced cell death. Here, we show that DTX1 is an E3 ligase for c-FLIP in gastric cancer cells. DTX1 promoted c-FLIP downregulation. Overexpression of DTX1 sensitized gastric cancer cells to TRAIL-induced apoptosis, whereas DTX1-knockdown attenuated apoptosis induction. DTX1 binds c-FLIP(L) and directs it into the endosome-lysosomal pathway for proteasome-independent degradation. Moreover, induction of DTX1 in AGS cells by geldanamycin conferred susceptibility of those cells to TRAIL-induced apoptosis. Our results reveal a tumor-suppressive role for DTX1 and suggest a new approach to increasing TRAIL efficacy by raising DTX1 levels in gastric cancer therapy. DTX1 also enhanced c-FLIP degradation and FasL-induced and TRAIL-induced apoptosis in T cells, suggesting that DTX1 constitutes one of the physiological mechanisms regulating c-FLIP stability. |
format | Online Article Text |
id | pubmed-5833402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58334022018-03-05 c-FLIP is a target of the E3 ligase deltex1 in gastric cancer Hsu, Tzu-Sheng Mo, Shu-Ting Hsu, Ping-Ning Lai, Ming-Zong Cell Death Dis Article The ubiquitin E3 ligase DELTEX1 (DTX1) is specifically downregulated in gastric cancer tissues, and expression of DTX1 is linked to better prognoses and survival in gastric cancer. Cellular FLICE inhibitory protein (c-FLIP) is known for its pivotal role in the resistance of cancer cells to death receptor-induced cell death. Here, we show that DTX1 is an E3 ligase for c-FLIP in gastric cancer cells. DTX1 promoted c-FLIP downregulation. Overexpression of DTX1 sensitized gastric cancer cells to TRAIL-induced apoptosis, whereas DTX1-knockdown attenuated apoptosis induction. DTX1 binds c-FLIP(L) and directs it into the endosome-lysosomal pathway for proteasome-independent degradation. Moreover, induction of DTX1 in AGS cells by geldanamycin conferred susceptibility of those cells to TRAIL-induced apoptosis. Our results reveal a tumor-suppressive role for DTX1 and suggest a new approach to increasing TRAIL efficacy by raising DTX1 levels in gastric cancer therapy. DTX1 also enhanced c-FLIP degradation and FasL-induced and TRAIL-induced apoptosis in T cells, suggesting that DTX1 constitutes one of the physiological mechanisms regulating c-FLIP stability. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5833402/ /pubmed/29374180 http://dx.doi.org/10.1038/s41419-017-0165-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hsu, Tzu-Sheng Mo, Shu-Ting Hsu, Ping-Ning Lai, Ming-Zong c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title | c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title_full | c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title_fullStr | c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title_full_unstemmed | c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title_short | c-FLIP is a target of the E3 ligase deltex1 in gastric cancer |
title_sort | c-flip is a target of the e3 ligase deltex1 in gastric cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833402/ https://www.ncbi.nlm.nih.gov/pubmed/29374180 http://dx.doi.org/10.1038/s41419-017-0165-6 |
work_keys_str_mv | AT hsutzusheng cflipisatargetofthee3ligasedeltex1ingastriccancer AT moshuting cflipisatargetofthee3ligasedeltex1ingastriccancer AT hsupingning cflipisatargetofthee3ligasedeltex1ingastriccancer AT laimingzong cflipisatargetofthee3ligasedeltex1ingastriccancer |