資料載入中.....
|
請使用永久網址來引用或連結此文件:
https://ir.cnu.edu.tw/handle/310902800/31739
|
| 標題: | Serglycin in tumor microenvironment promotes non-small cell lung cancer aggressiveness in a CD44-dependent manner |
| 作者: | Guo, J-Y
Hsu, H-S
Tyan, S-W
Li, F-Y
Shew, J-Y
Lee, W-H
Chen, J-Y |
| 貢獻者: | Acad Sinica, Inst Biomed Sci
Taipei Vet Gen Hosp, Dept Thorac Surg
Chia Nan Univ Pharm & Sci, Dept Biotechnol
Taipei Vet Gen Hosp, Dept Pathol
Acad Sinica, Genom Res Ctr
China Med Univ, Inst Clin Med
Natl Yang Ming Univ, Dept Life Sci
Natl Yang Ming Univ, Inst Genome Sci |
| 關鍵字: | Epithelial-Mesenchymal Transition
Nf-Kappa-B
Hepatocellular-Carcinoma
Colon-Cancer
Cd44
Fibroblasts
Expression
Overexpression
Activation
Adhesion |
| 日期: | 201-04-277 |
| 上傳時間: | 2018-11-30 15:54:53 (UTC+8) |
| 出版者: | Nature Publishing Group |
| 摘要: | Tumor microenvironment (TME) plays an active role in promoting tumor progression. To further understand the communication between TME and tumor cells, this study aimed at investigating the involvement of CD44, a type I cell surface receptor, in the crosstalk between tumor cells and TME. We have previously shown that chondroitin sulfate proteoglycan serglycin (SRGN), a CD44-interacting factor, was preferentially secreted by cancer-associated fibroblasts (CAFs) for promoting tumor growth in breast cancer patients. In this study, we show that SRGN is overexpressed in primary non-small cell lung cancers (NSCLCs), by both carcinoma and stromal cells. Using gain-of-function and loss-of-function approaches, we show that SRGN promotes NSCLC cell migration and invasion as well as colonization in the lung and liver in a CD44-dependent manner. SRGN induces lung cancer cell stemness, as demonstrated by its ability to enhance NSCLC cell sphere formation via Nanog induction, accompanied with increased chemoresistance and anoikis-resistance. SRGN promotes epithelial-mesenchymal transition by enhancing vimentin expression via CD44/NF-kappa B/claudin-1(CLDN1) axis. In support, CLDN1 and SRGN expression are tightly linked together in primary NSCLC. Most importantly, increased expression of SRGN and/or CLDN1 predicts poor prognosis in primary lung adenocarcinomas. In summary, we demonstrate that SRGN secreted by tumor cells and stromal components in the TME promotes malignant phenotypes through interacting with tumor cell receptor CD44, suggesting that a combined therapy targeting both CD44 and its ligands in the TME may be an attractive approach for cancer therapy. |
| 關聯: | Oncogene, v.36, n.17, pp.2457-2471 |
| 顯示於類別: | [生物科技系(所)] 期刊論文
|
文件中的檔案:
| 檔案 |
描述 |
大小 | 格式 | 瀏覽次數 |
|---|
| 10.1038-onc.2016.404.pdf | | 5427Kb | Adobe PDF | 0 | 檢視/開啟 | | index.html | | 0Kb | HTML | 1200 | 檢視/開啟 |
|
在CNU IR中所有的資料項目都受到原著作權保護.
|
