Abstract | BACKGROUND: OBJECTIVE/METHODS: This review focuses on the role of ER and ER co-activators in breast cancer and current approaches to targeting SRC co-factors for treatment of hormone-receptor-positive breast cancer. RESULTS/CONCLUSIONS: There is a drive to selectively apply aromatase inhibitors on the basis of either risk or biological evidence of resistance to tamoxifen treatment. Both strategies may yield improved treatment to benefit ratios.
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Authors | Melanie Spears, John Bartlett |
Journal | Expert opinion on therapeutic targets
(Expert Opin Ther Targets)
Vol. 13
Issue 6
Pg. 665-74
(Jun 2009)
ISSN: 1744-7631 [Electronic] England |
PMID | 19456271
(Publication Type: Journal Article, Review)
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Chemical References |
- Estrogen Receptor Modulators
- Estrogen Receptor alpha
- Estrogen Receptor beta
- Ligands
- MAS1 protein, human
- Proto-Oncogene Mas
- src-Family Kinases
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Topics |
- Breast Neoplasms
(drug therapy, enzymology, metabolism)
- Estrogen Receptor Modulators
(therapeutic use)
- Estrogen Receptor alpha
(drug effects, metabolism)
- Estrogen Receptor beta
(drug effects, metabolism)
- Humans
- Ligands
- Proto-Oncogene Mas
- Signal Transduction
- src-Family Kinases
(drug effects, metabolism)
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