English
| 正體中文 |
简体中文
|
全文筆數/總筆數 : 94201/94201 (100%)
造訪人次 : 81510126 線上人數 : 3151
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by
NTU Library IR team.
搜尋範圍
全部NCUIR
生醫理工學院
生醫科學與工程學系
--期刊論文
查詢小技巧:
您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
進階搜尋
主頁
‧
登入
‧
上傳
‧
說明
‧
關於NCUIR
‧
管理
NCU Institutional Repository
>
生醫理工學院
>
生醫科學與工程學系
>
期刊論文
>
Item 987654321/102985
資料載入中.....
書目資料匯出
Endnote RIS 格式資料匯出
Bibtex 格式資料匯出
引文資訊
資料載入中.....
資料載入中.....
請使用永久網址來引用或連結此文件:
https://ir.lib.ncu.edu.tw/handle/987654321/102985
題名:
SPANXA suppresses EMT by inhibiting c-JUN/SNAI2 signaling in lung adenocarcinoma
作者:
許藝瓊
;
Hsiao, Yi-Jing
;
Su, Kang-Yi
;
Hsu, Yi-Chiung
;
Chang, Gee-Chen
;
Chen, Jin-Shing
;
Chen, Hsuan-Yu
;
Hong, Qi-Sheng
;
Hsu, Shih-Chun
;
Kang, Po-Hsiang
;
Hsu, Chia-Ying
;
Ho, Bing-Ching
;
Yang, Tsung-Hui
;
Wang, Chia-Yu
;
Jou, Yuh-Shan
;
Yang, Pan-Chyr
;
Yu, Sung-Liang
貢獻者:
生醫理工學院生醫科學與工程學系
關鍵詞:
Adenocarcinoma - genetics
;
Adenocarcinoma - metabolism
;
Adenocarcinoma - pathology
;
Adenocarcinoma of Lung
;
Animals
;
Cell Line, Tumor
;
Epithelial-Mesenchymal Transition
;
Heterografts
;
Humans
;
Lung Neoplasms - genetics
;
Lung Neoplasms - metabolism
;
Lung Neoplasms - pathology
;
Mice
;
Mice, SCID
;
Nuclear Proteins - genetics
;
Nuclear Proteins - metabolism
;
Proto-Oncogene Proteins c-jun - antagonists & inhibitors
;
Proto-Oncogene Proteins c-jun - metabolism
;
Research Paper
;
Signal Transduction
;
Snail Family Transcription Factors - antagonists & inhibitors
;
Snail Family Transcription Factors - metabolism
;
Transfection
;
Up-Regulation
日期:
2016-01-01
上傳時間:
2026-04-23 11:21:25 (UTC+8)
出版者:
United States: Impact Journals LLC
摘要:
摘要: SPANXA (Sperm Protein Associated with the Nucleus on the X-chromosome, family members A1/A2) acts as a cancer-testis antigen expressed in normal testes, but dysregulated in various tumors. We found that SPANXA is highly expressed in low-invasive CL1-0 cells compared with isogenous high-invasive CL1-5 cells. SPANXA was preferably expressed in tumor tissues and associated with the prolonged survival of lung adenocarcinomas. SPANXA suppressed the invasion and metastasis of lung cancer cells in vitro and in vivo. By the expression microarray and pathway analysis, we found that the SPANXA-altered genes were enriched in the epithelial-mesenchymal transition (EMT) pathway. SPANXA reduced SNAI2 expression resulted in up-regulating E-cadherin. c-JUN acts as the positive-regulator of EMT. Silencing SPANXA increased c-JUN mRNA expression and blockage of c-JUN led to SNAI2 down-regulation. Our results clearly characterized SPANXA as an EMT inhibitor by suppressing c-JUN-SNAI2 axis in lung adenocarcinoma.
其他題名: Oncotarget
出版者: United States: Impact Journals LLC
出版日期: 2016-07-12
出處: Oncotarget, 2016-07, Vol.7 (28), p.44417-44429
版權: Copyright: © 2016 Hsiao et al. 2016
識別號: ISSN: 1949-2553
識別號: EISSN: 1949-2553
識別號: DOI: 10.18632/oncotarget.10088
識別號: PMID: 27323831
顯示於類別:
[生醫科學與工程學系] 期刊論文
文件中的檔案:
檔案
描述
大小
格式
瀏覽次數
index.html
0Kb
HTML
17
檢視/開啟
在NCUIR中所有的資料項目都受到原著作權保護.
社群 sharing
::: Copyright National Central University. | 國立中央大學圖書館版權所有 |
收藏本站
|
設為首頁
| 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
DSpace Software
Copyright © 2002-2004
MIT
&
Hewlett-Packard
/
Enhanced by
NTU Library IR team
Copyright ©
-
隱私權政策聲明