Ring box protein-1 is associated with a poor prognosis and tumor progression in esophageal cancer.

• 資料種別: 博士論文
• ISSN: 1792-1074
• タイトル: Ring box protein-1 is associated with a poor prognosis and tumor progression in esophageal cancer.
• 巻次・部編番号: 20 3
• 著者・編者: Kunishige, Tomohiro; Migita, Kazuhiro; Matsumoto, Sohei; Wakatsuki, Kohei; Nakade, Hiroshi; Miyao, Shintaro; Kuniyasu, Hiroki; Sho, Masayuki
• 著者標目: Kunishige, Tomohiro; Migita, Kazuhiro; Matsumoto, Sohei; Wakatsuki, Kohei; Nakade, Hiroshi; Miyao, Shintaro; Kuniyasu, Hiroki; Sho, Masayuki
• 出版事項: Spandidos Publications
• 出版年月日等: 2020-09; 20 3
• 出版年（W3CDTF）: 2020-09
• 並列タイトル等: Ring box protein-1 は食道癌の予後不良因子であり、腫瘍の進行と関連している
• タイトル（掲載誌）: Oncology letters
• 授与機関名: 奈良県立医科大学
• 授与年月日: 2020-12-24
• 授与年月日（W3CDTF）: 2020-12-24
• 報告番号: 乙第1480号
• 学位: 博士（医学）
• 博論授与番号: 乙第1480号
• 本文の言語コード: eng
• 件名標目: ring box protein-1; prognostic factor; proliferation; chemotherapy; esophageal cancer
• 対象利用者: 一般
• 一般注記: type:Thesis; Ring box protein-1 (RBX1) is an essential component of the S-phase kinase-associated protein, Cullin and F-box containing ubiquitin ligases. Overexpression of RBX1 has been reported in several cancer types; however, little is known regarding the prognostic value and role of RBX1 in esophageal cancer. The present study examined 120 patients with esophageal cancer (EC) who underwent curative esophagectomy and 61 patients with EC who underwent neoadjuvant combination chemotherapy with docetaxel, cisplatin and 5-fluorouracil (5-FU; DCF) using immunohistochemistry. All specimens were classified into two groups according to the percentage of RBX1-positive tumor cells. In addition, the impact of RBX1 expression on cancer cell proliferation was analyzed in vitro using a small interfering RNA silencing technique. RBX1 expression levels showed significant differences according to tumor size (P<0.001), tumor depth (P=0.002), lymph node metastasis (P=0.004), pathological stage (P=0.001), lymphatic invasion (P=0.001) and venous invasion (P=0.001). The overall survival (OS) rate in the RBX1 high expression group was significantly lower compared with that in the low group (P=0.004). Multivariate analysis demonstrated that RBX1 status was an independent prognostic factor. RBX1 gene silencing inhibited the proliferation of human EC cells and enhanced the antitumor effect of 5-FU. Among patients who underwent neoadjuvant DCF therapy, the RBX1 high expression group had a significantly lower OS rate compared with that of the RBX1-low group (P<0.001). In conclusion, RBX1 has notable prognostic value, and RBX1 may serve an important function in the tumor progression of EC.; 博士（医学）・乙第1480号・令和2年12月24日; Copyright: © Kunishigeet al. This is an open access article distributed under theterms of CreativeCommons Attribution License(https://creativecommons.org/licenses/by-nc-nd/4.0/).; identifier:Oncology letters Vol.20 No.3 p.2919-2927 (2020 Sep); identifier:17921074; identifier:http://ginmu.naramed-u.ac.jp/dspace/handle/10564/3825; identifier:Oncology letters, 20(3): 2919-2927
• DOI: info:doi/10.3892/ol.2020.11840; https://doi.org/info:doi/10.3892/ol.2020.11840
• 国立国会図書館永続的識別子: info:ndljp/pid/11674105; https://dl.ndl.go.jp/pid/11674105
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文; https://dl.ndl.go.jp/collections/A00014
• 収集根拠: 博士論文（自動収集）
• 受理日（W3CDTF）: 2021-05-23T18:24:43+09:00
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: http://hdl.handle.net/10564/3825
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

目次

2024-05-04 再収集

2024-05-04 再収集

2024-05-04 再収集