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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-4054876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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