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Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer

The B-cell lymphoma/leukemia 2 protein (BCL-2) may help many types of cancers to evade cell death. However, identifying exactly where this is the case is a challenge. ABT-199 is a small molecule that selectively inhibits BCL-2, which is currently in clinical trials in lymphoid malignancies. While in...

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Detalles Bibliográficos
Autores principales: Deng, Jing, Letai, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054876/
https://www.ncbi.nlm.nih.gov/pubmed/24172207
http://dx.doi.org/10.1186/bcr3568
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author Deng, Jing
Letai, Anthony
author_facet Deng, Jing
Letai, Anthony
author_sort Deng, Jing
collection PubMed
description The B-cell lymphoma/leukemia 2 protein (BCL-2) may help many types of cancers to evade cell death. However, identifying exactly where this is the case is a challenge. ABT-199 is a small molecule that selectively inhibits BCL-2, which is currently in clinical trials in lymphoid malignancies. While inhibiting BCL-2 by itself can cause cell death in hematopoietic tumors, single-agent activity is harder to observe in solid tumors. Combining ABT-199 with tamoxifen, the standard endocrine therapy for estrogen receptor-positive breast cancers, 85% of which have BCL-2 expression, represents a new strategy to prime cancer cells for apoptosis and elicit better cancer cell death responses.
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spelling pubmed-40548762014-06-12 Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer Deng, Jing Letai, Anthony Breast Cancer Res Viewpoint The B-cell lymphoma/leukemia 2 protein (BCL-2) may help many types of cancers to evade cell death. However, identifying exactly where this is the case is a challenge. ABT-199 is a small molecule that selectively inhibits BCL-2, which is currently in clinical trials in lymphoid malignancies. While inhibiting BCL-2 by itself can cause cell death in hematopoietic tumors, single-agent activity is harder to observe in solid tumors. Combining ABT-199 with tamoxifen, the standard endocrine therapy for estrogen receptor-positive breast cancers, 85% of which have BCL-2 expression, represents a new strategy to prime cancer cells for apoptosis and elicit better cancer cell death responses. BioMed Central 2013 2013-10-31 /pmc/articles/PMC4054876/ /pubmed/24172207 http://dx.doi.org/10.1186/bcr3568 Text en Copyright © 2013 BioMed Central Ltd.
spellingShingle Viewpoint
Deng, Jing
Letai, Anthony
Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title_full Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title_fullStr Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title_full_unstemmed Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title_short Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER(+) breast cancer
title_sort priming bcl-2 to kill: the combination therapy of tamoxifen and abt-199 in er(+) breast cancer
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054876/
https://www.ncbi.nlm.nih.gov/pubmed/24172207
http://dx.doi.org/10.1186/bcr3568
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