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...
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Series: | Breast Cancer: Basic and Clinical Research |
Online Access: | https://doi.org/10.1177/1178223417749855 |
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doaj-fbe43642dda44887a02413569a3ffe1d2020-11-25T03:00:30ZengSAGE PublishingBreast Cancer: Basic and Clinical Research1178-22342018-01-011210.1177/1178223417749855TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin CotreatmentJasmine M Manouchehri0Katherine A Turner1Michael Kalafatis2Center for Gene Regulation in Health and Disease (GRHD), Cleveland State University, Cleveland, OH, USACenter for Gene Regulation in Health and Disease (GRHD), Cleveland State University, Cleveland, OH, USADepartment of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USABreast 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.https://doi.org/10.1177/1178223417749855 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jasmine M Manouchehri Katherine A Turner Michael Kalafatis |
spellingShingle |
Jasmine M Manouchehri Katherine A Turner Michael Kalafatis TRAIL-Induced Apoptosis in TRAIL-Resistant Breast Carcinoma Through Quercetin Cotreatment Breast Cancer: Basic and Clinical Research |
author_facet |
Jasmine M Manouchehri Katherine A Turner Michael Kalafatis |
author_sort |
Jasmine M Manouchehri |
title |
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_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_sort |
trail-induced apoptosis in trail-resistant breast carcinoma through quercetin cotreatment |
publisher |
SAGE Publishing |
series |
Breast Cancer: Basic and Clinical Research |
issn |
1178-2234 |
publishDate |
2018-01-01 |
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. |
url |
https://doi.org/10.1177/1178223417749855 |
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