Literature DB >> 15956720

Signaling pathways of the LGR7 and LGR8 receptors determined by reporter genes.

Michelle L Halls1, Ross A Bathgate, Peter J Roche, Roger J Summers.   

Abstract

Although much is known about the pleiotropic effects mediated by relaxin, the exact signaling pathways involved remain relatively elusive. This study examines LGR7 and LGR8 signaling using reporter gene technology. The greatest response was observed at the CRE reporter (indicates activation of cAMP-PKA and p38/JNK pathways), although INSL3 treatment of LGR8 produced a lower response than H2 relaxin treatment of LGR7. AP1 (which indicates activation of JNK pathways) was stimulated to a lesser degree. Three other reporters produced no response. The reporter gene studies suggest that ligand stimulation of LGR7 and LGR8 involves cAMP-PKA and p38/JNK signaling.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15956720     DOI: 10.1196/annals.1282.043

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  2 in total

1.  Dual blockade of PKA and NF-κB inhibits H2 relaxin-mediated castrate-resistant growth of prostate cancer sublines and induces apoptosis.

Authors:  Ruth L Vinall; Christopher M Mahaffey; Ryan R Davis; Zunping Luo; Regina Gandour-Edwards; Paramita M Ghosh; Clifford G Tepper; Ralph W de Vere White
Journal:  Horm Cancer       Date:  2011-08       Impact factor: 3.869

2.  Relaxin induces matrix-metalloproteinases-9 and -13 via RXFP1: induction of MMP-9 involves the PI3K, ERK, Akt and PKC-ζ pathways.

Authors:  Nisar Ahmad; Wei Wang; Remi Nair; Sunil Kapila
Journal:  Mol Cell Endocrinol       Date:  2012-07-24       Impact factor: 4.102

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.