Literature DB >> 20426700

PAR-4 as a possible new target for pancreatic cancer therapy.

Asfar S Azmi1, Philip A Philip, Syed F Zafar, Fazlul H Sarkar, Ramzi M Mohammad.   

Abstract

IMPORTANCE OF THE FIELD: Pancreatic cancer (PC) is a deadly disease that is intractable to currently available treatment regimens. Although well described in different tumors types, the importance of apoptosis inducer prostate apoptosis response-4 (Par-4) in PC has not been appreciated. PC is an oncogenic kras driven disease, which is known to downregulate Par-4. Therefore, this review highlights its significance and builds a strong case supporting the role of Par-4 as a possible therapeutic target in PC. AREAS COVERED IN THIS REVIEW: Literature-based evidence spanning the last 15 years on Par-4 and its significance in PC. WHAT THE READER WILL GAIN: This review provides comprehensive knowledge of the significance of Par-4 and its association with kras status in PC, along with the crosstalk with crucial resistance and survival molecules NF-kappaB and Bcl-2 that ultimately are responsible for the overall poor outcome of different therapeutic approaches in this disease. TAKE HOME MESSAGE: Par-4 holds promise as a potential therapeutic target that can be induced by chemopreventive agents and small-molecule inhibitors either alone or in combination with standard chemotherapeutics leading to selective apoptosis in PC cells. It also acts as a chemosensitizer and therefore warrants further clinical investigations in this disease.

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Year:  2010        PMID: 20426700      PMCID: PMC2883466          DOI: 10.1517/14728222.2010.487066

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  93 in total

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Review 5.  BCL-2 family antagonists for cancer therapy.

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6.  KRAS mutations: an old oncogene becomes a new predictive biomarker.

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Review 9.  Apoptosis by Par-4 in cancer and neurodegenerative diseases.

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7.  Inhibition of AKT promotes FOXO3a-dependent apoptosis in prostate cancer.

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8.  Post-translational regulation of the cleaved fragment of Par-4 in ovarian and endometrial cancer cells.

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  9 in total

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