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
相关论文
共 192 条
[81]   Pancreatic intraepithelial neoplasia -: A new nomenclature and classification system for pancreatic duct lesions [J].
Hruban, RH ;
Adsay, NV ;
Albores-Saavedra, J ;
Compton, C ;
Garrett, ES ;
Goodman, SN ;
Kern, SE ;
Klimstra, DS ;
Klöppel, G ;
Longnecker, DS ;
Lüttges, J ;
Offerhaus, GJA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (05) :579-586
[82]   Towards personalized, tumour-specific, therapeutic vaccines for cancer [J].
Hu, Zhuting ;
Ott, Patrick A. ;
Wu, Catherine J. .
NATURE REVIEWS IMMUNOLOGY, 2018, 18 (03) :168-182
[83]   Hepatocyte growth factor attenuates renal fibrosis through TGF-β1 suppression by apoptosis of myofibroblasts [J].
Iekushi, Kazuma ;
Taniyama, Yoshiaki ;
Azuma, Junya ;
Sanada, Fumihiro ;
Kusunoki, Hiroshi ;
Yokoi, Toyohiko ;
Koibuchi, Nobutaka ;
Okayama, Keita ;
Rakugi, Hiromi ;
Morishita, Ryuichi .
JOURNAL OF HYPERTENSION, 2010, 28 (12) :2454-2461
[84]   Hyaluronan impairs vascular function and drug delivery in a mouse model of pancreatic cancer [J].
Jacobetz, Michael A. ;
Chan, Derek S. ;
Neesse, Albrecht ;
Bapiro, Tashinga E. ;
Cook, Natalie ;
Frese, Kristopher K. ;
Feig, Christine ;
Nakagawa, Tomoaki ;
Caldwell, Meredith E. ;
Zecchini, Heather I. ;
Lolkema, Martijn P. ;
Jiang, Ping ;
Kultti, Anne ;
Thompson, Curtis B. ;
Maneval, Daniel C. ;
Jodrell, Duncan I. ;
Frost, Gregory I. ;
Shepard, H. M. ;
Skepper, Jeremy N. ;
Tuveson, David A. .
GUT, 2013, 62 (01) :112-U153
[85]   Novel allogeneic granulocyte-macrophage colony-stimulating factor-secreting tumor vaccine for pancreatic cancer: A phase I trial of safety and immune activation [J].
Jaffee, EM ;
Hruban, RH ;
Biedrzycki, B ;
Laheru, D ;
Schepers, K ;
Sauter, PR ;
Goemann, M ;
Coleman, J ;
Grochow, L ;
Donehower, RC ;
Lillemoe, KD ;
O'Reilly, S ;
Abrams, RA ;
Pardoll, DM ;
Cameron, JL ;
Yeo, CJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (01) :145-156
[86]   Crosstalk between Regulatory T Cells and Tumor-Associated Dendritic Cells Negates Anti-tumor Immunity in Pancreatic Cancer [J].
Jang, Jung-Eun ;
Hajdu, Cristina H. ;
Liot, Caroline ;
Miller, George ;
Dustin, Michael L. ;
Bar-Sagi, Dafna .
CELL REPORTS, 2017, 20 (03) :558-571
[87]   Inhibition of CCR2 potentiates checkpoint inhibitor immunotherapy in murine model of pancreatic cancer [J].
Janson, Christine ;
Jung, Heiyoun ;
Ertl, Linda ;
Liu, Shirley ;
Dang, Ton ;
Zeng, Yibin ;
Krasinski, Antoni ;
McMahon, Jeff ;
Zhang, Penglie ;
Charo, Israel ;
Singh, Rajinder ;
Schall, Thomas J. .
CANCER RESEARCH, 2017, 77
[88]   Development of resistance to FAK inhibition in pancreatic cancer is linked to stromal depletion [J].
Jiang, Hong ;
Liu, Xiuting ;
Knolhoff, Brett L. ;
Hegde, Samarth ;
Lee, Kyung Bae ;
Jiang, Hongmei ;
Fields, Ryan C. ;
Pachter, Jonathan A. ;
Lim, Kian-Huat ;
DeNardo, David G. .
GUT, 2020, 69 (01) :122-132
[89]   Targeting focal adhesion kinase renders pancreatic cancers responsive to checkpoint immunotherapy [J].
Jiang, Hong ;
Hegde, Samarth ;
Knolhoff, Brett L. ;
Zhu, Yu ;
Herndon, John M. ;
Meyer, Melissa A. ;
Nywening, Timothy M. ;
Hawkins, William G. ;
Shapiro, Irina M. ;
Weaver, David T. ;
Pachter, Jonathan A. ;
Wang-Gillam, Andrea ;
DeNardo, David G. .
NATURE MEDICINE, 2016, 22 (08) :851-+
[90]   Comprehensive analysis of matrix metalloproteinase and tissue inhibitor expression in pancreatic cancer: Increased expression of matrix metalloproteinase-7 predicts poor survival [J].
Jones, LE ;
Humphreys, MJ ;
Campbell, F ;
Neoptolemos, JP ;
Boyd, MT .
CLINICAL CANCER RESEARCH, 2004, 10 (08) :2832-2845