イチノエ アキマサ
Ichinoe Akimasa
一戸 晶元 所属 医学部 医学科(附属足立医療センター) 職種 講師 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Identification of the Critical Site of Calponin 1 for Suppression of Ovarian Cancer Properties. |
掲載誌名 | 正式名:Anticancer research 略 称:Anticancer Res ISSNコード:02507005/17917530 |
巻・号・頁 | 35(11),pp.5996-5999 |
著者・共著者 | TAKAKO YAMANE†, KAZUO ASANOMA, HIROAKI KOBAYASHI, GE LIU, HIROSHI YAGI, TATSUHIRO OHGAMI, AKIMASA ICHINOE, KENZO SONODA, NORIO WAKE, KIYOKO KATO |
発行年月 | 2015/11 |
概要 | Background: Although several studies have
demonstrated the tumor suppressive function of CNN1 (calponin 1), no studies have performed a site-specific analysis of CNN1 on tumor cell activities. Materials and Methods: We herein studied the site-specific effects of CNN1 in ovarian cancer cells using full-length CNN1 (fCNN1), three CNN1 repeats (3CNRs), or the first CNN1 repeat (CNR1) expression vectors. Ovarian cancer cells stably expressing each construct were analyzed for in vitro proliferation, cell motility, invasion, and soft agar assays. An in vitro model of pleural dissemination was also established. Results: Cell proliferation, anchorageindependent colony formation, cell motility, and cell invasion were all suppressed in fCNN1, 3CNRs, and CNR1- stably-expressing cells. CNN1 expression in mesothelial cells suppressed cancer cell invasion into a monolayer of mesothelial cells. Conclusion: CNR1 showed similar suppressive effects as fCNN1. Results suggest CNR1 as a potential small synthetic peptide candidate for therapeutic strategies against ovarian cancer. |