Pancreatic cancer: The microenvironment needs attention too!

被引:69
作者
Apte, M. V. [1 ,2 ]
Xu, Z. [1 ,2 ]
Pothula, S. [1 ,2 ]
Goldstein, D. [1 ,3 ,4 ]
Pirola, R. C. [1 ,2 ]
Wilson, J. S. [1 ,2 ]
机构
[1] Univ New South Wales, South Western Sydney Clin Sch, Pancreat Res Grp, Fac Med, Sydney, NSW, Australia
[2] Ingham Inst Appl Med Res, Sydney, NSW, Australia
[3] Prince Wales Hosp, Dept Med Oncol, Sydney, NSW, Australia
[4] Univ New South Wales, Fac Med, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Pancreatic stellate cells; Pancreatic ductal adenocarcinoma; Stromal-tumour interactions; Pancreatic fibrogenesis; Pancreatic cancer; Tumour microenvironment;
D O I
10.1016/j.pan.2015.02.013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The abundant stromal/desmoplastic reaction, a characteristic feature of a majority of pancreatic adenocarcinomas (PDAC), has only recently been receiving some attention regarding its possible role in the pathobiology of pancreatic cancer. It is now well established that the cells predominantly responsible for producing the collagenous stroma are pancreatic stellate cells (PSCs). In addition to extracellular matrix proteins, the stroma also exhibits cellular elements including, immune cells, endothelial cells and neural cells. Evidence is accumulating to indicate the presence of significant interactions between PSCs and cancer cells as well as between PSCs and other cell types in the stroma. The majority of research reports to date, using in vitro and in vivo approaches, suggest that these interactions facilitate local growth as well as distant metastasis of pancreatic cancer, although a recent study using animals depleted of myofibroblasts has raised some questions regarding the central role of myofibroblasts in cancer progression. Nonetheless, novel therapeutic strategies have been assessed, mainly in the pre-clinical setting, in a bid to interrupt stromal-tumour interactions and inhibit disease progression. The next important challenge is for the translation of such pre-clinical strategies to the clinical situation so as to improve the outcome of patients with pancreatic cancer. Copyright (C) 2015, IAP and EPC. Published by Elsevier India, a division of Reed Elsevier India Pvt. Ltd. All rights reserved.
引用
收藏
页码:S32 / S38
页数:7
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