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FAK and paxillin, two potential targets in pancreatic cancer

Pancreatic ductal adenocarcinoma (PDAC) is a devastating cancer in large part due to late diagnosis and a lack of effective screening tests. In spite of recent progress in imaging, surgery and new therapeutic options for pancreatic cancer, the overall five-year survival still remains unacceptably lo...

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Autores principales: Kanteti, Rajani, Batra, Surinder K., Lennon, Frances E., Salgia, Ravi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058780/
https://www.ncbi.nlm.nih.gov/pubmed/26980710
http://dx.doi.org/10.18632/oncotarget.8040
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author Kanteti, Rajani
Batra, Surinder K.
Lennon, Frances E.
Salgia, Ravi
author_facet Kanteti, Rajani
Batra, Surinder K.
Lennon, Frances E.
Salgia, Ravi
author_sort Kanteti, Rajani
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) is a devastating cancer in large part due to late diagnosis and a lack of effective screening tests. In spite of recent progress in imaging, surgery and new therapeutic options for pancreatic cancer, the overall five-year survival still remains unacceptably low. Numerous studies have shown that focal adhesion kinase (FAK) is activated in many cancers including PDAC and promotes cancer progression and metastasis. Paxillin, an intracellular adaptor protein that plays a key role in cytoskeletal organization, connects integrins to FAK and plays a key role in assembly and disassembly of focal adhesions. Here, we have reviewed evidence in support of FAK as a potential therapeutic target and summarized related combinatorial therapies.
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spelling pubmed-50587802016-10-15 FAK and paxillin, two potential targets in pancreatic cancer Kanteti, Rajani Batra, Surinder K. Lennon, Frances E. Salgia, Ravi Oncotarget Review Pancreatic ductal adenocarcinoma (PDAC) is a devastating cancer in large part due to late diagnosis and a lack of effective screening tests. In spite of recent progress in imaging, surgery and new therapeutic options for pancreatic cancer, the overall five-year survival still remains unacceptably low. Numerous studies have shown that focal adhesion kinase (FAK) is activated in many cancers including PDAC and promotes cancer progression and metastasis. Paxillin, an intracellular adaptor protein that plays a key role in cytoskeletal organization, connects integrins to FAK and plays a key role in assembly and disassembly of focal adhesions. Here, we have reviewed evidence in support of FAK as a potential therapeutic target and summarized related combinatorial therapies. Impact Journals LLC 2016-03-13 /pmc/articles/PMC5058780/ /pubmed/26980710 http://dx.doi.org/10.18632/oncotarget.8040 Text en Copyright: © 2016 Kanteti et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Kanteti, Rajani
Batra, Surinder K.
Lennon, Frances E.
Salgia, Ravi
FAK and paxillin, two potential targets in pancreatic cancer
title FAK and paxillin, two potential targets in pancreatic cancer
title_full FAK and paxillin, two potential targets in pancreatic cancer
title_fullStr FAK and paxillin, two potential targets in pancreatic cancer
title_full_unstemmed FAK and paxillin, two potential targets in pancreatic cancer
title_short FAK and paxillin, two potential targets in pancreatic cancer
title_sort fak and paxillin, two potential targets in pancreatic cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058780/
https://www.ncbi.nlm.nih.gov/pubmed/26980710
http://dx.doi.org/10.18632/oncotarget.8040
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