Literature DB >> 27374183

Pancreatic cancer actionable genes in precision medicine and personalized surgery.

Juehua Yu1, Shi-He Liu1, Robbi Sanchez1, John Nemunaitis2, Enrique Rozengurt3, F Charles Brunicardi4.   

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a deadly cancer with an overall 5-year survival rate less than 5% due to the poor early diagnosis and lack of effective therapeutic options. The most effective therapy remains surgery, however post-operative survival could be enhanced with effective adjuvant therapy. The massive information gained from Omics techniques on PDAC at the beginning of the 21st century is a remarkable accomplishment. However, the information gained from the omics data, including next generation sequencing data, has yet to successfully affect care of patients suffering with PDAC. Therefore, we propose the development of an actionable genomic platform that matches a patient's PDAC clinically actionable genes with potential targeted adjuvant therapies. Using this platform, PDX1 has been identified as a potential actionable gene for PDAC, therefore, RNAi therapy, gene therapy and small inhibitory drugs, all targeting PDX1, serve as potential targeted adjuvant therapies. Preclinical studies support the hypothesis that identification of PDAC actionable genes could permit translation of a patient's genomic information into precision targeted adjuvant therapy for PDAC.
Copyright © 2016 Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Actionable genes; Molecular surgery; Pancreatic cancer

Mesh:

Year:  2016        PMID: 27374183      PMCID: PMC5195911          DOI: 10.1016/j.surge.2016.05.002

Source DB:  PubMed          Journal:  Surgeon        ISSN: 1479-666X            Impact factor:   2.392


  55 in total

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3.  Persistent expression of PDX-1 in the pancreas causes acinar-to-ductal metaplasia through Stat3 activation.

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4.  Timing is everything: Brca2 and p53 mutations in pancreatic cancer.

Authors:  Jennifer P Morton; Colin W Steele; Owen J Sansom
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5.  Activation of the Wnt pathway through Wnt2 promotes metastasis in pancreatic cancer.

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Journal:  Am J Cancer Res       Date:  2014-09-06       Impact factor: 6.166

Review 6.  Pancreatic cancer genomics.

Authors:  David K Chang; Sean M Grimmond; Andrew V Biankin
Journal:  Curr Opin Genet Dev       Date:  2014-01-28       Impact factor: 5.578

Review 7.  Personalized cancer approach: using RNA interference technology.

Authors:  John Nemunaitis; Donald D Rao; Shi-He Liu; F Charles Brunicardi
Journal:  World J Surg       Date:  2011-08       Impact factor: 3.352

8.  Identification of K-ras mutations in pancreatic juice in the early diagnosis of pancreatic cancer.

Authors:  P Berthélemy; M Bouisson; J Escourrou; N Vaysse; J L Rumeau; L Pradayrol
Journal:  Ann Intern Med       Date:  1995-08-01       Impact factor: 25.391

9.  Metformin inhibition of mTORC1 activation, DNA synthesis and proliferation in pancreatic cancer cells: dependence on glucose concentration and role of AMPK.

Authors:  James Sinnett-Smith; Krisztina Kisfalvi; Robert Kui; Enrique Rozengurt
Journal:  Biochem Biophys Res Commun       Date:  2012-11-15       Impact factor: 3.575

10.  Specific gene expression and therapy for pancreatic cancer using the cytosine deaminase gene directed by the rat insulin promoter.

Authors:  Xiao-Ping Wang; Kazuyuki Yazawa; Jie Yang; Deborah Kohn; William E Fisher; F Charles Brunicardi
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  1 in total

Review 1.  Liquid biopsy in pancreatic cancer: the beginning of a new era.

Authors:  Dipesh Kumar Yadav; Xueli Bai; Rajesh Kumar Yadav; Alina Singh; Guogang Li; Tao Ma; Wei Chen; Tingbo Liang
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  1 in total

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