Targeting the PI3K/Akt signaling pathway in gastric carcinoma: A reality for personalized medicine?
Frequent activation of phosphatidylinositol-3 kinases(PI3K)/Akt/m TOR signaling pathway in gastric cancer(GC) is gaining immense popularity with identification of mutations and/or amplifications of PIK3 CA gene or loss of function of PTEN,a tumor suppressor protein,to name a few; both playing a cruc...
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Published in | World journal of gastroenterology : WJG Vol. 21; no. 43; pp. 12261 - 12273 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
United States
Baishideng Publishing Group Inc
21.11.2015
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Subjects | |
Online Access | Get full text |
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Summary: | Frequent activation of phosphatidylinositol-3 kinases(PI3K)/Akt/m TOR signaling pathway in gastric cancer(GC) is gaining immense popularity with identification of mutations and/or amplifications of PIK3 CA gene or loss of function of PTEN,a tumor suppressor protein,to name a few; both playing a crucial role in regulating this pathway. These aberrations result in dysregulation of this pathway eventually leading to gastric oncogenesis,hence,there is a need for targeted therapy for more effective anticancer treatment. Several inhibitors are currently in either preclinical or clinical stages for treatment of solid tumors like GC. With so many inhibitors under development,further studies on predictive biomarkers are needed to measure the specificity of any therapeutic intervention. Herein,we review the common dysregulation of PI3K/Akt/m TOR pathway in GC and the various types of single or dual pathway inhibitors under development that might have a superior role in GC treatment. We also summarize the recent developments in identification of predictive biomarkers and propose use of predictive biomarkers to facilitate more personalized cancer therapy with effective PI3K/Akt/m TOR pathway inhibition. |
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Bibliography: | Epidemiology;Gastric cancer;PI3K/Akt/ m TOR pathwa Frequent activation of phosphatidylinositol-3 kinases(PI3K)/Akt/m TOR signaling pathway in gastric cancer(GC) is gaining immense popularity with identification of mutations and/or amplifications of PIK3 CA gene or loss of function of PTEN,a tumor suppressor protein,to name a few; both playing a crucial role in regulating this pathway. These aberrations result in dysregulation of this pathway eventually leading to gastric oncogenesis,hence,there is a need for targeted therapy for more effective anticancer treatment. Several inhibitors are currently in either preclinical or clinical stages for treatment of solid tumors like GC. With so many inhibitors under development,further studies on predictive biomarkers are needed to measure the specificity of any therapeutic intervention. Herein,we review the common dysregulation of PI3K/Akt/m TOR pathway in GC and the various types of single or dual pathway inhibitors under development that might have a superior role in GC treatment. We also summarize the recent developments in identification of predictive biomarkers and propose use of predictive biomarkers to facilitate more personalized cancer therapy with effective PI3K/Akt/m TOR pathway inhibition. Shikha Satendra Singh;Wei Ney Yap;Frank Arfuso;Shreya Kar;Chao Wang;Wanpei Cai;Arunasalam M Dharmarajan;Gautam Sethi;Alan Prem Kumar;Cancer Science Institute of Singapore,National University of Singapore;Department of Pharmacology,Yong Loo Lin School of Medicine,National University of Singapore;Davos Life Science Pte Ltd;School of Biomedical Sciences,Curtin Health Innovation Research Institute,Curtin University;National University Cancer Institute;Department of Biological Sciences,University of North Texas ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Author contributions: Singh SS, Yap WN, Arfuso F, Kar S, Wang C, Cai W did the research and wrote the draft review paper; Dharmarajan MA, Sethi G and Kumar AP did all the editing and inclusion of additional information for the final review paper. Telephone: +65-65165456 Fax: +65-68739664 Correspondence to: Dr. Alan Prem Kumar, PhD, Cancer Science Institute of Singapore, National University of Singapore, Singapore City 117597, Singapore. csiapk@nus.edu.sg |
ISSN: | 1007-9327 2219-2840 2219-2840 |
DOI: | 10.3748/wjg.v21.i43.12261 |