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8/29/2014 2:41:00 PM | Browse: 719 | Download: 557
Publication Name World Journal of Gastroenterology
Manuscript ID 6588
Country Taiwan
Received
2013-10-24 18:06
Peer-Review Started
2013-10-25 18:55
To Make the First Decision
2013-12-16 17:53
Return for Revision
2013-12-18 10:16
Revised
2013-12-26 09:33
Second Decision
2014-02-27 11:20
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-02-27 11:27
Articles in Press
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-03-26 19:02
Publish the Manuscript Online
2014-04-14 10:49
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 Biochemistry & Molecular Biology
Manuscript Type Topic Highlights
Article Title Somatic alterations in mitochondrial DNA and mitochondrial dysfunction in gastric cancer progression
Manuscript Source Invited Manuscript
All Author List Hsin-Chen Lee, Kuo-Hung Huang, Tien-Shun Yeh and Chin-Wen Chi
Funding Agency and Grant Number
Funding Agency Grant Number
Center of Excellence for Cancer Research at Taipei Veterans General, the Ministry of Health and Welfare DOH102-TDC-111-007
Ministry of Education, Aim for the Top University Plan
National Science Council, Taiwan NSC101-2320-B-010-068-MY3
Corresponding Author Hsin-Chen Lee, Professor, Institute of Pharmacology, School of Medicine, National Yang-Ming University, No. 155, Li-Nong St., Sec. 2, Taipei 112, Taiwan. hclee2@ym.edu.tw
Key Words Gastric cancer; Somatic mitochondrial DNA mutations; Mitochondrial dysfunction
Core Tip In this review, we summarize recent somatic mitochondrial DNA (mtDNA) alterations identified in gastric cancer, and the relationship between these alterations and the clinicopathological features of gastric cancer. We suggest that point mutations and mtDNA copy number decreases are the two most common mtDNA alterations that potentially result in mitochondrial dysfunction in gastric cancer. Mitochondrial dysfunction-generated reactive oxygen species may be involved in the malignant changes of gastric cancer. The search for strategies to prevent the mtDNA alterations and inhibit the mitochondrial retrograde signaling will benefit the development of novel treatments for gastric cancer and other malignancies.
Publish Date 2014-04-14 10:49
Citation Lee HC, Huang KH, Yeh TS, Chi CW. Somatic alterations in mitochondrial DNA and mitochondrial dysfunction in gastric cancer progression. World J Gastroenterol 2014; 20(14): 3950-3959
URL http://www.wjgnet.com/1007-9327/full/v20/i14/3950.htm
DOI http://dx.doi.org/10.3748/wjg.v20.i14.3950
Full Article (PDF) WJG-20-3950.pdf
Full Article (Word) WJG-20-3950.doc
Manuscript File 6588-Review.docx
Answering Reviewers 6588-Answering reviewers.pdf
Copyright License Agreement 6588-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate 6588-Language certificate.pdf
Peer-review Report 6588-Peer review.pdf
Scientific Editor Work List 6588-Scientific editor work list.doc