The tumour microenvironment in pancreatic cancer - clinical challenges and opportunities

被引:857
作者
Ho, Won Jin [1 ,2 ]
Jaffee, Elizabeth M. [1 ,2 ]
Zheng, Lei [1 ,2 ]
机构
[1] Johns Hopkins Univ, Skip Viragh Pancreat Canc Ctr Clin Res & Care, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Bloomberg Kimmel Inst Immunotherapy, Baltimore, MD USA
关键词
COLONY-STIMULATING FACTOR; FOCAL ADHESION KINASE; REGULATORY T-CELLS; MATRIX-METALLOPROTEINASE; DUCTAL ADENOCARCINOMA; STELLATE CELLS; INTRAEPITHELIAL NEOPLASIA; INFILTRATING MACROPHAGES; PEPTIDE VACCINATION; IMMUNE ACTIVATION;
D O I
10.1038/s41571-020-0363-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal solid tumours despite the use of multi-agent conventional chemotherapy regimens. Such poor outcomes have fuelled ongoing efforts to exploit the tumour microenvironment (TME) for therapy, but strategies aimed at deconstructing the surrounding desmoplastic stroma and targeting the immunosuppressive pathways have largely failed. In fact, evidence has now shown that the stroma is multi-faceted, which illustrates the complexity of exploring features of the TME as isolated targets. In this Review, we describe ways in which the PDAC microenvironment has been targeted and note the current understanding of the clinical outcomes that have unexpectedly contradicted preclinical observations. We also consider the more sophisticated therapeutic strategies under active investigation - multi-modal treatment approaches and exploitation of biologically integrated targets - which aim to remodel the TME against PDAC. Important research efforts are being made to develop therapeutic strategies targeting the tumour microenvironment in pancreatic adenocarcinoma. The authors of this Review describe the apparent contradiction between preclinical studies and clinical outcomes observed to date, presenting more sophisticated strategies under active investigation.
引用
收藏
页码:527 / 540
页数:14
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