Literature DB >> 20159523

Novel targets for pancreatic cancer therapy.

Philip A Philip1.   

Abstract

Pancreatic adenocarcinoma (PDA) is one of the cancers that is resistant to most conventional anticancer therapies. PDA-affected patients show a poor prognosis. The 5-year survival rate for PDA is 5% and has changed little over the past few decades. This has prompted extensive research to identify new agents that can be used for anticancer therapy. The only cytotoxic drug that has been approved by the Food and Drug Administration (FDA) is gemcitabine, which offers marginal benefits to patients in terms of symptom control and prolongation of life. Various strategies like targeting the epidermal growth factor receptor pathway and vascular endothelial growth factor receptor pathway have been researched upon. But these strategies have not provided promising results and none of the FDA-approved targeted agents have added any substantial clinical benefit to gemcitabine except for a marginal benefit from erlotinib. This article discusses various possible new targets and new agents for the anticancer therapy for PDA.

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Year:  2010        PMID: 20159523     DOI: 10.1016/j.soc.2009.11.012

Source DB:  PubMed          Journal:  Surg Oncol Clin N Am        ISSN: 1055-3207            Impact factor:   3.495


  6 in total

1.  Bioengineered human arginase I with enhanced activity and stability controls hepatocellular and pancreatic carcinoma xenografts.

Authors:  Evan S Glazer; Everett M Stone; Cihui Zhu; Katherine L Massey; Amir N Hamir; Steven A Curley
Journal:  Transl Oncol       Date:  2011-06-01       Impact factor: 4.243

2.  Suppression of the epidermal growth factor receptor inhibits epithelial-mesenchymal transition in human pancreatic cancer PANC-1 cells.

Authors:  Zhi-Gang Chang; Jun-Min Wei; Chang-Fu Qin; Kun Hao; Xiao-Dong Tian; Kun Xie; Xue-Hai Xie; Yin-Mo Yang
Journal:  Dig Dis Sci       Date:  2012-01-21       Impact factor: 3.199

3.  In vitro and in vivo anti-tumor activities of a gemcitabine derivative carried by nanoparticles.

Authors:  Brian R Sloat; Michael A Sandoval; Dong Li; Woon-Gye Chung; Dharmika S P Lansakara-P; Philip J Proteau; Kaoru Kiguchi; John DiGiovanni; Zhengrong Cui
Journal:  Int J Pharm       Date:  2011-03-01       Impact factor: 5.875

4.  Dual blockade of epidermal growth factor receptor and insulin-like growth factor receptor-1 signaling in metastatic pancreatic cancer: phase Ib and randomized phase II trial of gemcitabine, erlotinib, and cixutumumab versus gemcitabine plus erlotinib (SWOG S0727).

Authors:  Philip A Philip; Bryan Goldman; Ramesh K Ramanathan; Heinz-Josef Lenz; Andrew M Lowy; Robert P Whitehead; Takeru Wakatsuki; Syma Iqbal; Rakesh Gaur; Jacqueline K Benedetti; Charles D Blanke
Journal:  Cancer       Date:  2014-07-16       Impact factor: 6.860

5.  Psorinum therapy in treating stomach, gall bladder, pancreatic, and liver cancers: a prospective clinical study.

Authors:  Aradeep Chatterjee; Jaydip Biswas; Ashim Chatterjee; Sudin Bhattacharya; Bishnu Mukhopadhyay; Syamsundar Mandal
Journal:  Evid Based Complement Alternat Med       Date:  2010-12-08       Impact factor: 2.629

6.  Inhibiting the growth of pancreatic adenocarcinoma in vitro and in vivo through targeted treatment with designer gold nanotherapeutics.

Authors:  Rachel A Kudgus; Annamaria Szabolcs; Jameel Ahmad Khan; Chad A Walden; Joel M Reid; J David Robertson; Resham Bhattacharya; Priyabrata Mukherjee
Journal:  PLoS One       Date:  2013-03-06       Impact factor: 3.240

  6 in total

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