タナベ ケンジ
Tanabe Kenji
田邊 賢司 所属 研究施設 研究施設 職種 准教授 |
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論文種別 | 総説 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Involvement of a novel ADP-ribosylation factor GTPase-activating protein, SMAP, in membrane trafficking: implications in cancer cell biology. |
掲載誌名 | 正式名:Cancer science |
巻・号・頁 | 97,pp.801-806 |
著者・共著者 | Tanabe, Kenji Kon, Shunsuke Natsume, Waka Torii, Tetsuo Watanabe, Toshio Satake, Masanobu |
担当区分 | 筆頭著者 |
発行年月 | 2006 |
概要 | The endocytosis of cell membrane proteins is initiated by the binding of activated Arf6, a member of Ras-related GTPases, to the PM. A GAP specific for Arf6 triggers the budding of endocytotic vesicles from the PM by inactivating GTP-bound Arf6. We recently identified the SMAP gene that encodes an ArfGAP and is involved in the endocytosis of TfnR and possibly E-cadherin. In this review, we summarize the process of intracellular membrane trafficking, highlighting the roles played by the SMAP gene. Progression of cancer to malignancy occurs in parallel with the disappearance of E-cadherin, a central component of the adherens junction in epithelial cells. Therefore, elucidation of the molecular mechanism of E-cadherin endocytosis should be one of the key elements in tumor cell biology. |