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

被引:18
作者
Azmi, Asfar S. [1 ]
Philip, Philip A. [2 ]
Zafar, Syed F. [2 ]
Sarkar, Fazlul H. [1 ]
Mohammad, Ramzi M. [2 ]
机构
[1] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Hematol Oncol, Detroit, MI 48201 USA
关键词
apoptosis; pancreatic cancer; Par-4; NF-KAPPA-B; SMALL-MOLECULE INHIBITOR; TUMOR-SUPPRESSOR PAR-4; ZIPPER PROTEIN PAR-4; PRO-APOPTOTIC GENE; PHASE-II TRIAL; PROSTATE-CANCER; DOWN-REGULATION; KRAS MUTATIONS; K-RAS;
D O I
10.1517/14728222.2010.487066
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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-kappa B 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.
引用
收藏
页码:611 / 620
页数:10
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