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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 
 
 

A common polymorphism renders the luteinizing hormone receptor protein more active by improving signal peptide function and predicts adverse outcome in breast cancer patients.

CONTEXT: Epidemiological and animal studies indicate a carcinogenic role of estrogens in breast tissue. The pituitary gonadotropin LH is an important regulator of estrogen production in premenopausal women, whereas even in women after menopause, 10-25% of ovarian steroid hormone production is LH dependent. OBJECTIVE: We hypothesized that an LH receptor ( LHR) gene variant may affect LHR function and thereby influence disease outcome in breast cancer patients. DESIGN: The association of a polymorphic CTCCAG (Leu-Gln) insertion (insLQ), in the signal peptide encoded by exon 1 of the LHR gene with breast cancer risk, (disease-free) survival, and clinicopathological features was studied in a large cohort of 751 breast cancer patients with complete follow-up. Functional analysis of the insLQ- LHR and non-LQ- LHR (no LQ insertion) was carried out using transfection studies. RESULTS: We found a significant association between the insLQ- LHR and a shorter disease-free survival (hazard ratio, 1.34; confidence interval, 1.11-1.63; P = 0.003). The mechanism of the effect of insLQ on LHR function involves increased receptor sensitivity (insLQ- LHR has a 1.9 times lower EC(50) than non-LQ- LHR; P = 0.02) and plasma membrane expression (insLQ- LHR has 1.4 times higher B(max); P = 0.0006) rendering the insLQ- LHR allele more active. CONCLUSIONS: The insLQ polymorphism increases LHR activity, thereby shortening breast cancer disease-free survival, probably by increasing estrogen exposure in female carriers.[1]

References

  1. A common polymorphism renders the luteinizing hormone receptor protein more active by improving signal peptide function and predicts adverse outcome in breast cancer patients. Piersma, D., Berns, E.M., Verhoef-Post, M., Uitterlinden, A.G., Braakman, I., Pols, H.A., Themmen, A.P. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
 
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