The role of pancreatic stellate cells in pancreatic cancer

被引:62
|
作者
Moir, John A. G. [1 ,2 ]
Mann, Jelena [2 ]
White, Steve A. [1 ]
机构
[1] Freeman Rd Hosp, Dept HPB & Transplant Surg, Newcastle Upon Tyne NE7 7XL, Tyne & Wear, England
[2] Inst Cellular Med, Fibrosis Lab, Newcastle Upon Tyne, Tyne & Wear, England
来源
SURGICAL ONCOLOGY-OXFORD | 2015年 / 24卷 / 03期
关键词
Pancreatic cancer; Pancreatic stellate cells; Tumour stroma; EXTRACELLULAR-MATRIX; TRANSFORMING GROWTH-FACTOR-BETA-1; MESENCHYMAL TRANSITION; MALIGNANT PHENOTYPE; INDUCE FIBROSIS; I COLLAGEN; EXPRESSION; METASTASIS; CARCINOMA; HYPOXIA;
D O I
10.1016/j.suronc.2015.05.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The prognosis of pancreatic cancer remains desperately poor, with little progress made over the past 30 years despite the development of new combination chemotherapy regimens. Stromal activity is especially prominent in the tissue surrounding pancreatic tumours, and has a profound influence in dictating tumour development and dissemination. Pancreatic stellate cells (PaSCs) have a key role in this tumour microenvironment, and have been the subject of much research in the past decade. This review examines the relationship between PaSCs and cancer cells. Methods: A comprehensive literature search was performed of multiple databases up to March 2014, including Medline, Pubmed and Google Scholar. Results: A complex bidirectional interplay exists between PaSCs and cancer cells, resulting in a perpetuating loop of increased activity and an overriding pro-tumorigenic effect. This involves a number of signalling pathways that also impacts on other stromal components and vasculature, contributing to chemoresistance. The Reverse Warburg Effect is also introduced as a novel concept in tumour stroma. Conclusion: This review highlights the pancreatic tumour microenvironment, and in particular PaSCs, as an ideal target for therapeutics. There are a number of cellular processes involving PaSCs which could hold the key to more effectively treating pancreatic cancer. The feasibility of targeting these pathways warrant further in depth investigation, with the aim of reducing the aggressiveness of pancreatic cancer and improving chemodelivery. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:232 / 238
页数:7
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