Cargando…

TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment

Breast cancer is the most commonly diagnosed cancer in women. There is a continued interest for the development of more efficacious treatment regimens for breast carcinoma. Recombinant human tumor necrosis factor–related apoptosis-inducing ligand (rhTRAIL) shows potential as a potent anticancer ther...

Descripción completa

Detalles Bibliográficos
Autores principales: Manouchehri, Jasmine M, Turner, Katherine A, Kalafatis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802616/
https://www.ncbi.nlm.nih.gov/pubmed/29434473
http://dx.doi.org/10.1177/1178223417749855
_version_ 1783298555396489216
author Manouchehri, Jasmine M
Turner, Katherine A
Kalafatis, Michael
author_facet Manouchehri, Jasmine M
Turner, Katherine A
Kalafatis, Michael
author_sort Manouchehri, Jasmine M
collection PubMed
description Breast cancer is the most commonly diagnosed cancer in women. There is a continued interest for the development of more efficacious treatment regimens for breast carcinoma. Recombinant human tumor necrosis factor–related apoptosis-inducing ligand (rhTRAIL) shows potential as a potent anticancer therapeutic for the treatment of breast cancer, whereas displaying minimal toxicity to normal cells. However, the promise of rhTRAIL for the treatment of breast cancer is dismissed by the resistance to rhTRAIL-induced apoptosis exhibited by many breast cancers. Thus, a cotreatment strategy was examined by applying the natural compound quercetin (Q) as a sensitizing agent for rhTRAIL-resistant breast cancer BT-20 and MCF-7 cells. Quercetin was able to sensitize rhTRAIL-resistant breast cancers to rhTRAIL-induced apoptosis as detected by Western blotting through the proteasome-mediated degradation of c-FLIP(L) and through the upregulation of DR5 expression transcriptionally. Overall, these in vitro findings establish that Q is an effective sensitizing agent for rhTRAIL-resistant breast cancers.
format Online
Article
Text
id pubmed-5802616
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-58026162018-02-12 TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment Manouchehri, Jasmine M Turner, Katherine A Kalafatis, Michael Breast Cancer (Auckl) Original Research Breast cancer is the most commonly diagnosed cancer in women. There is a continued interest for the development of more efficacious treatment regimens for breast carcinoma. Recombinant human tumor necrosis factor–related apoptosis-inducing ligand (rhTRAIL) shows potential as a potent anticancer therapeutic for the treatment of breast cancer, whereas displaying minimal toxicity to normal cells. However, the promise of rhTRAIL for the treatment of breast cancer is dismissed by the resistance to rhTRAIL-induced apoptosis exhibited by many breast cancers. Thus, a cotreatment strategy was examined by applying the natural compound quercetin (Q) as a sensitizing agent for rhTRAIL-resistant breast cancer BT-20 and MCF-7 cells. Quercetin was able to sensitize rhTRAIL-resistant breast cancers to rhTRAIL-induced apoptosis as detected by Western blotting through the proteasome-mediated degradation of c-FLIP(L) and through the upregulation of DR5 expression transcriptionally. Overall, these in vitro findings establish that Q is an effective sensitizing agent for rhTRAIL-resistant breast cancers. SAGE Publications 2018-01-15 /pmc/articles/PMC5802616/ /pubmed/29434473 http://dx.doi.org/10.1177/1178223417749855 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Manouchehri, Jasmine M
Turner, Katherine A
Kalafatis, Michael
TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title_full TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title_fullStr TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title_full_unstemmed TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title_short TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment
title_sort trail-induced apoptosis in trail-resistant breast carcinoma through quercetin cotreatment
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802616/
https://www.ncbi.nlm.nih.gov/pubmed/29434473
http://dx.doi.org/10.1177/1178223417749855
work_keys_str_mv AT manouchehrijasminem trailinducedapoptosisintrailresistantbreastcarcinomathroughquercetincotreatment
AT turnerkatherinea trailinducedapoptosisintrailresistantbreastcarcinomathroughquercetincotreatment
AT kalafatismichael trailinducedapoptosisintrailresistantbreastcarcinomathroughquercetincotreatment