HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The potential role of estrogen receptors and the SRC family as targets for the treatment of breast cancer.

AbstractBACKGROUND:
Breast cancer has a number of subtypes, the main ones are estrogen-receptor (ER)-positive, luminal type A and B. Treatment selection, with respect to hormonal therapy, is based upon ER expression. Whilst for ER-positive cancers, endocrine therapy is highly successful in the adjuvant setting, a significant proportion of cancers exhibit hormone resistance, often associated with altered growth factor receptor or ER signalling. Modulation of steroid receptor function by receptor co-activators or repressors is a potential mechanism of resistance. The p160 or SRC proto-oncogene family of co-activators are important in breast cancer response to endocrine therapy and can act as a paradigm of co-activator function.
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.
AuthorsMelanie Spears, John Bartlett
JournalExpert opinion on therapeutic targets (Expert Opin Ther Targets) Vol. 13 Issue 6 Pg. 665-74 (Jun 2009) ISSN: 1744-7631 [Electronic] England
PMID19456271 (Publication Type: Journal Article, Review)
Chemical References
  • Estrogen Receptor Modulators
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Ligands
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • src-Family Kinases
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)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: