TY - JOUR
T1 - GPCRs as potential therapeutic targets in preeclampsia
AU - McGuane, J. T.
AU - Conrad, K. P.
PY - 2012
Y1 - 2012
N2 - Preeclampsia is an important obstetric complication that arises in 5% of women after the 20th week of gestation, for which there is no specific therapy and no cure. Although much of the recent investigation in this field has focused on soluble forms of the angiogenic membrane receptor tyrosine kinase Flt1 and the transforming growth factor b co-receptor Endoglin, there is significant clinical potential for several GPCR targets and their agonists or antagonists in preeclampsia. In this review, we discuss several of the most promising candidates in this category, including calcitonin receptor- like receptor/receptor activity modifying protein 1 complexes, the angiotensin AT1, 2 and Mas receptors, and the relaxin receptor RXFP1. We also address some of the controversies surrounding the roles and therapeutic potential of these GPCRs and their (ant)agonists in preeclampsia.
AB - Preeclampsia is an important obstetric complication that arises in 5% of women after the 20th week of gestation, for which there is no specific therapy and no cure. Although much of the recent investigation in this field has focused on soluble forms of the angiogenic membrane receptor tyrosine kinase Flt1 and the transforming growth factor b co-receptor Endoglin, there is significant clinical potential for several GPCR targets and their agonists or antagonists in preeclampsia. In this review, we discuss several of the most promising candidates in this category, including calcitonin receptor- like receptor/receptor activity modifying protein 1 complexes, the angiotensin AT1, 2 and Mas receptors, and the relaxin receptor RXFP1. We also address some of the controversies surrounding the roles and therapeutic potential of these GPCRs and their (ant)agonists in preeclampsia.
UR - http://www.scopus.com/inward/record.url?scp=84871438596&partnerID=8YFLogxK
U2 - 10.1016/j.ddmod.2012.05.001
DO - 10.1016/j.ddmod.2012.05.001
M3 - Review article
SN - 1740-6757
VL - 9
SP - e119-e127
JO - Drug Discovery Today: Disease Models
JF - Drug Discovery Today: Disease Models
IS - 3
ER -