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ID 112899
タイトル別表記
Nab-paclitaxelはin vitroでC-X-C motif chemokine 10を介したinterleukin-6制御により癌-間質相互作用を抑制する
著者
馮, 睿 徳島大学大学院医科学教育部(医学専攻)
キーワード
130nm albumin-bound paclitaxel
cancer-associated fibroblast
C-X-C motif chemokine 10
epithelial-mesenchymal transition
pancreatic neoplasms
chemokine CXCL10
資料タイプ
学位論文
抄録
Cancer‐associated fibroblasts (CAF), derived from stroma of cancer tissues, interact with cancer cells and play an important role in cancer initiation, growth, and metastasis. Nab‐paclitaxel (nab‐PTX) is a 130 nm albumin‐binding paclitaxel and recommended for many types of cancer chemotherapy. The nab‐PTX stromal‐disrupting effect during pancreatic cancer treatment has been reported. The aim of the present study was to determine the role of nab‐PTX in cancer cells and CAF interaction. Cancer cells (MIA PaCa‐2 and Panc‐1) were cocultured with CAF or treated with CAF conditioned medium, after which their migration and invasion ability, epithelial‐mesenchymal transition (EMT)‐related marker expression and C‐X‐C motif chemokine 10 (CXCL10) expression and secretion were detected. Nab‐PTX treatment was carried out during the coculture system or during preparation of CAF conditioned medium. Then cancer cell migration and invasion ability, EMT‐related marker expression, CXCL10 expression and secretion, and interleukin‐6 (IL‐6) expression and secretion by CAF were checked After coculture with CAF, migration and invasion ability of cancer cells increased. CAF also downregulated E‐cadherin and upregulated N‐cadherin and vimentin expression in cancer cells. During coculture or stimulation with cancer cell‐cultured medium, CAF significantly increased IL‐6 expression and secretion. However, nab‐PTX in the coculture system canceled CAF‐induced migration and invasion promotion and EMT-related gene changes. Moreover, nab‐PTX increased CXCL10 expression of cancer cells which blocked CAF IL‐6 expression and secretion. Nab‐PTX treatment could increase CXCL10 expression of cancer cells which blocks CAF cancer cell migration and invasion‐promoting effect by inhibiting IL‐6 expression.
掲載誌名
Cancer Science
ISSN
13497006
cat書誌ID
AA12100165
出版者
Wiley|Japanese Cancer Association
109
8
開始ページ
2509
終了ページ
2519
発行日
2018-06-14
備考
内容要旨・審査要旨・論文本文の公開
本論文は, 著者Rui Fengの学位論文として提出され, 学位審査・授与の対象となっている。
権利情報
© 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
EDB ID
出版社版DOI
出版社版URL
フルテキストファイル
言語
eng
著者版フラグ
博士論文全文を含む
文科省報告番号
甲第3242号
学位記番号
甲医第1391号
学位授与年月日
2018-10-25
学位名
博士(医学)
学位授与機関
徳島大学
部局
医学系
病院