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There is accumulating evidence that shows close relationship between (P)RR and autophagy. Soluble (P)RR consisting of the extracellular domain of (P)RR is generated from (P)RR by proteolytic enzymes. The aim of the present study was to clarify the influence of autophagy inhibition on soluble (P)RR expression in cancer cells. Autophagy was inhibited by treatment of bafilomycin A1 or chloroquine in MCF\u20107 and A549 cells for 72\u00a0hr. Western blot analysis showed that protein levels of soluble (P)RR were markedly elevated by autophagy inhibition, whereas no noticeable increases were observed in full\u2010length (P)RR. Secretion of soluble (P)RR into the medium was increased dose\u2010dependently by bafilomycin A1 or chloroquine. Autophagy inhibition was confirmed by enhanced accumulation of autophagy\u2010related proteins, LC3, p62 and LAMP1 in intracellular vesicles. Increased amount of soluble (P)RR by autophagy inhibition was decreased by site\u20101 protease inhibitor, whereas no noticeable increase in site\u20101 protease immunoreactivity was observed in cells with autophagy inhibition by immunocytochemistry. These findings suggest that soluble (P)RR protein accumulates by autophagy inhibition, possibly because of the reduced degradation of soluble (P)RR in the intracellular vesicles during autophagy inhibition.<\/jats:p>","DOI":"10.1111\/gtc.12776","type":"journal-article","created":{"date-parts":[[2020,4,21]],"date-time":"2020-04-21T03:55:29Z","timestamp":1587441329000},"page":"483-497","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Increased soluble (pro)renin receptor protein by autophagy inhibition in cultured cancer cells"],"prefix":"10.1111","volume":"25","author":[{"given":"Moe","family":"Endo","sequence":"first","affiliation":[{"name":"Department of Endocrinology and Applied Medical Science Tohoku University Graduate School of Medicine Sendai Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Koji","family":"Ohba","sequence":"additional","affiliation":[{"name":"Department of Endocrinology 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