A Starring Role for Stellate Cells in the Pancreatic Cancer Microenvironment

被引:398
作者
Apte, Minoti V. [1 ,2 ]
Wilson, Jeremy S. [1 ,2 ]
Lugea, Aurelia [1 ,3 ,4 ]
Pandol, Stephen J. [1 ,3 ,4 ,5 ]
机构
[1] Univ New S Wales, Pancreat Res Grp, Sydney, NSW, Australia
[2] Univ New S Wales, Fac Med, South Western Sydney Clin Sch, Sydney, NSW, Australia
[3] Dept Vet Affairs, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
[5] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
关键词
Pancreatic Stellate Cells; Pancreatic Cancer; Inflammation; Immune Surveillance; NERVE GROWTH-FACTOR; DUCTAL ADENOCARCINOMA; TRANSFORMING GROWTH-FACTOR-BETA-1; INDUCE FIBROSIS; GENE-EXPRESSION; POOR-PROGNOSIS; BETA-CATENIN; OXIDIZED LDL; MOUSE MODEL; KAPPA-B;
D O I
10.1053/j.gastro.2012.11.037
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Pancreatic ductal adenocarcinoma is a devastating disease, and patient outcomes have not improved in decades. Treatments that target tumor cells have largely failed. This could be because research has focused on cancer cells and the influence of the stroma on tumor progression has been largely ignored. The focus of pancreatic cancer research began to change with the identification of pancreatic stellate cells, which produce the pancreatic tumor stroma. There is compelling in vitro and in vivo evidence for the influence of pancreatic stellate cells on pancreatic cancer development; several recent preclinical studies have reported encouraging results with approaches designed to target pancreatic stellate cells and the stroma. We review the background and recent advances in these areas, along with important areas of future research that could improve therapy.
引用
收藏
页码:1210 / 1219
页数:10
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