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A study of signaling blocks involved in ACSM of relaxin in comparison with that of insulin previously detected showed a close similarity throughout the post\u2010receptor signaling chain of both hormones. The inhibitory action of tyrosine kinase blockers on the hormone AC activating effect indicates that the relaxin receptor involved in ACSM is likely to be of the tyrosine kinase type. However, a recent discovery of a relaxin receptor with serpentine architecture leaves open the question concerning the existence of receptor of the tyrosine kinase type. The structural\u2010functional organization of the ACSM due to the action of relaxin\u2014shown here for the first time\u2014can be presented as the following signaling sequence: relaxin receptor \u21d2 G<jats:sub>i<\/jats:sub> protein (\u03b2\u03b3\u2010dimer) \u21d2 phosphatidylinositol 3\u2010kinase \u21d2 protein kinase C\u03b6 \u21d2 G<jats:sub>s<\/jats:sub> protein \u21d2 adenylyl cyclase. According to our hypothesis, the regulatory action of the insulin superfamily peptides on cell processes (proliferation, apoptosis, and metabolism) is mediated via ACSM.<\/jats:p>","DOI":"10.1016\/j.cellbi.2005.12.015","type":"journal-article","created":{"date-parts":[[2006,3,3]],"date-time":"2006-03-03T12:34:11Z","timestamp":1141389251000},"page":"533-540","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Adenylyl cyclase signaling mechanisms of relaxin and insulin action: Similarities and 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