Contribution of Epithelial-to-Mesenchymal Transition and Cancer Stem Cells to Pancreatic Cancer Progression

被引:102
作者
Krantz, Seth B. [2 ]
Shields, Mario A. [1 ]
Dangi-Garimella, Surabhi [1 ]
Munshi, Hidayatullah G. [1 ,3 ,4 ]
Bentrem, David J. [2 ,3 ,4 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Surg, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[4] Jesse Brown VA Med Ctr, Chicago, IL USA
关键词
pancreatic cancer; epithelial-mesenchymal transition; microRNA; stem cells; drug resistance; TGF-BETA; LIVER FIBROSIS; MIR-200; FAMILY; TRANSCRIPTIONAL REGULATION; DRUG-RESISTANCE; SPLICE VARIANTS; UP-REGULATION; TUMOR-GROWTH; HEDGEHOG; EXPRESSION;
D O I
10.1016/j.jss.2011.09.020
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
Pancreatic adenocarcinoma remains among the most lethal of human malignancies. Overall 5-y survival is less than 5%, and only 20% of patients presenting with localized disease amenable to surgical resection. Even in patients who undergo resection, long-term survival remains extremely poor. A major contributor to the aggressiveness of multiple cancers, and pancreatic cancer in particular, is the process of epithelial-to-mesenchymal transition (EMT). This review highlights the growing evidence of EMT in pancreatic cancer progression, focusing on the contribution of EMT to the development of cancer stem cells and on interaction of EMT with other pathways central to cancer progression, such as Hedgehog signaling, the K-ras oncogene, and transforming growth factor-beta (TGF-beta). We will also discuss EMT-targeting agents currently in development and in clinical trials that may help to reduce the morbidity and mortality associated with pancreatic cancer. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:105 / 112
页数:8
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