Title |
Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER+ breast cancer
|
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Published in |
Breast Cancer Research, October 2013
|
DOI | 10.1186/bcr3568 |
Pubmed ID | |
Authors |
Jing Deng, Anthony Letai |
Abstract |
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. |
X Demographics
Geographical breakdown
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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United States | 1 | 3% |
Unknown | 32 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 10 | 30% |
Researcher | 6 | 18% |
Student > Bachelor | 4 | 12% |
Student > Master | 2 | 6% |
Professor | 1 | 3% |
Other | 3 | 9% |
Unknown | 7 | 21% |
Readers by discipline | Count | As % |
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Agricultural and Biological Sciences | 10 | 30% |
Biochemistry, Genetics and Molecular Biology | 7 | 21% |
Pharmacology, Toxicology and Pharmaceutical Science | 3 | 9% |
Medicine and Dentistry | 3 | 9% |
Chemistry | 2 | 6% |
Other | 1 | 3% |
Unknown | 7 | 21% |