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8/20/2014 6:38:00 PM | Browse: 999 | Download: 768
Publication Name World Journal of Gastroenterology
Manuscript ID 6830
Country China
Received
2013-10-29 12:40
Peer-Review Started
2013-10-29 17:38
To Make the First Decision
2013-12-16 17:41
Return for Revision
2013-12-20 13:34
Revised
2014-02-13 18:09
Second Decision
2014-04-09 09:18
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-04-09 10:58
Articles in Press
2014-05-23 10:10
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-08-20 10:42
Publish the Manuscript Online
2014-08-20 18:38
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 Topic Highlights
Article Title Novel therapeutic targets for pancreatic cancer
Manuscript Source Invited Manuscript
All Author List Shing-Chun Tang and Yang-Chao Chen
Funding Agency and Grant Number
Corresponding Author Yang-Chao Chen, Professor, School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China. frankch@cuhk.edu.hk
Key Words Pancreatic cancer; CTHRC1; RAC1; RalGEF-RAl; Notch Signaling; Nodal/Activin Signaling; NDRG1; Hypoxic condition; DR5; PAR2; HER3; IAP; Non-coding RNA; HDAC; BMI1; EZH2; Pancreatic cancer stem cell; Tumour microenvironment
Core Tip Some of the targets discussed here have been discovered to enhance the effectiveness of gemcitabine upon co-administration of the corresponding agents, for instance, hyaluronidase can deplete hyaluronan in stromal region to enhance gemcitabine delivery. Besides, some signaling molecules, e.g., RalGEF-RAl, Rac1, and PAR2 are being targeted to suppress metastasis. Tumour proliferation is limited upon DR5 activated apoptosis and others promising therapeutic areas like epigenetic modifiers; IAP, miR, lncRNA, and cancer stem cells-tumour microenvironment will also be discussed.
Publish Date 2014-08-20 18:38
Citation Tang SC, Chen YC. Novel therapeutic targets for pancreatic cancer. World J Gastroenterol 2014; 20(31): 10825-10844
URL http://www.wjgnet.com/1007-9327/full/v20/i31/10825.htm
DOI http://dx.doi.org/10.3748/wjg.v20.i31.10825
Full Article (PDF) WJG-20-10825.pdf
Full Article (Word) WJG-20-10825.doc
Manuscript File 6830-Review.docx
Answering Reviewers 6830-Answering reviewers.pdf
Copyright License Agreement 6830-Copyright assignment.pdf
Peer-review Report 6830-Peer review(s).pdf
Scientific Editor Work List 6830-Scientific editor work list.doc