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8/28/2014 9:54:00 AM | Browse: 613 | Download: 447
Publication Name World Journal of Gastroenterology
Manuscript ID 6825
Country China
Received
2013-10-29 12:18
Peer-Review Started
2013-10-30 08:55
To Make the First Decision
2013-12-26 11:35
Return for Revision
2013-12-27 15:42
Revised
2014-01-03 16:49
Second Decision
2014-02-27 11:21
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-02-27 11:26
Articles in Press
Publication Fee Transferred
Edit the Manuscript by Language Editor
2014-03-29 21:39
Typeset the Manuscript
2014-04-18 19:25
Publish the Manuscript Online
2014-05-14 10:58
ISSN 1007-9327 (print) and 2219-2840 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Medicine, Research & Experimental
Manuscript Type Autobiography
Article Title Growth inhibition of hepatocellular carcinoma tumor endothelial cells by miR-204-3p and underlying mechanism
Manuscript Source Invited Manuscript
All Author List Zhong-Hui Cui, Shi-Qiang Shen, Zu-Bing Chen and Chao Hu
Funding Agency and Grant Number
Corresponding Author Shi-Qiang Shen, MD, Department of General Surgery, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei Province, China. swsw2212@sina.com
Key Words Tumor vascular endothelial cells of hepatocellular carcinoma; Hepatic sinusoidal endothelial cells; MiRNA microarray; Mir-204-3p; Fibronectin 1
Core Tip This study first employed a microarray to detect differentially expressed miRNAs in hepatocellular carcinoma (HCC) tumor endothelial cells (TECs), as compared to hepatic sinusoidal endothelial cells with the goal of identifying specific miRNAs that play important roles in the angiogenesis of HCC. Our study proved that fibronectin 1 (FN1) is a potential target gene of miR-204-3p, suggesting that FN1 regulates the growth of HCC TECs via the miR-204-3p/FN1 signaling pathway. The underlying mechanism was also investigated to provide new targets and a theoretical basis for the anti-angiogenic gene therapy of HCC.
Publish Date 2014-05-14 10:58
Citation Cui ZH, Shen SQ, Chen ZB, Hu C. Growth inhibition of hepatocellular carcinoma tumor endothelial cells by miR-204-3p and underlying mechanism. World J Gastroenterol 2014; 20(18): 5493-5504
URL http://www.wjgnet.com/1007-9327/full/v20/i18/5493.htm
DOI http://dx.doi.org/10.3748/wjg.v20.i18.5493
Full Article (PDF) WJG-20-5493.pdf
Full Article (Word) WJG-20-5493.doc
Manuscript File 6825-Review.doc
Answering Reviewers 6825-Answering reviewers.pdf
Copyright License Agreement 6825-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate 6825-Language certificate.doc
Peer-review Report 6825-Peer review(s).pdf
Scientific Editor Work List 6825-Scientific editor work list.doc