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Publication Name World Journal of Gastroenterology
Manuscript ID 8215
Country Germany
Received
2013-12-22 11:31
Peer-Review Started
2013-12-23 12:19
To Make the First Decision
2014-01-24 12:03
Return for Revision
2014-01-25 16:15
Revised
Second Decision
2014-04-09 08:21
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-04-09 09:09
Articles in Press
2014-05-23 09:43
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-06-09 15:13
Publish the Manuscript Online
2014-06-27 10:37
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 Gastroenterology & Hepatology
Manuscript Type Autobiography
Article Title Distinct antifibrogenic effects of erlotinib, sunitinib and sorafenib on rat pancreatic stellate cells
Manuscript Source Unsolicited Manuscript
All Author List Anne Elsner, Falko Lange, Brit Fitzner, Martin Heuschkel, Bernd Joachim Krause and Robert Jaster
Funding Agency and Grant Number
Funding Agency Grant Number
Deutsche Forschungsgemeinschaft to RJ
Corresponding Author Robert Jaster, MD, Department of Medicine Ⅱ, Division of Gastroenterology, University Medicine Rostock, E.-Heydemann-Str. 6, 18057 Rostock, Germany. jaster@med.uni-rostock.de
Key Words Pancreatic stellate cell; Fibrosis; Erlotinib; Sunitinib; Sorafenib
Core Tip There are no specific therapies available to treat pancreatic fibrosis, a key feature of chronic pancreatitis and pancreatic cancer. Here we show that three clinically available small molecule kinase inhibitors (SMI), erlotinib, sunitinib and sorafenib, exert antifibrogenic effects in vitro by inhibiting key functions of rat pancreatic stellate cells (PSC), the main source of extracellular matrix proteins in the diseased pancreas. Furthermore, additive effects of the drugs were observed. Our studies also provide insight into molecular mechanisms of SMI action in PSC. We suggest that the antifibrotic efficiency of SMI, especially sorafenib, should be further evaluated in preclinical studies.
Publish Date 2014-06-27 10:37
Citation Elsner A, Lange F, Fitzner B, Heuschkel M, Krause BJ, Jaster R. Distinct antifibrogenic effects of erlotinib, sunitinib and sorafenib on rat pancreatic stellate cells. World J Gastroenterol 2014; 20(24): 7914-7925
URL http://www.wjgnet.com/1007-9327/full/v20/i24/7914.htm
DOI http://dx.doi.org/10.3748/wjg.v20.i24.7914
Full Article (PDF) WJG-20-7914.pdf
Full Article (Word) WJG-20-7914.doc
Manuscript File 8215-Review.doc
Answering Reviewers 8215-Answering reviewers.pdf
Copyright License Agreement 8215-Copyright assignment.pdf
Peer-review Report 8215-Peer review(s).pdf
Scientific Editor Work List 8215-Scientific editor work list.doc