Targeting the tumor microenvironment in pancreatic ductal adenocarcinoma

被引:23
|
作者
Pandey, Veethika [1 ]
Storz, Peter [1 ]
机构
[1] Mayo Clin, Dept Canc Biol, Jacksonville, FL 32224 USA
基金
美国国家卫生研究院;
关键词
Pancreatic cancer; tumor microenvironment; stellate cells; fibroblasts; tumor-associated macrophages; myeloid derived suppressor cells; MYELOID SUPPRESSOR-CELLS; STELLATE CELLS; T-CELL; EXTRACELLULAR-MATRIX; CANCER-CELLS; STIMULATING PROLIFERATION; POTENTIAL MECHANISMS; IMMUNE SUPPRESSION; ANTITUMOR-ACTIVITY; MACROPHAGES;
D O I
10.1080/14737140.2019.1622417
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The dismally slow improvement in patient survival over the years for pancreatic cancer patients is mainly due to two factors: the late diagnosis, at which point the disease is spread to distant organs; and the fact that tumor cells are surrounded by a dense, highly immunosuppressive microenvironment. The tumor microenvironment not only shields pancreatic cancer cells from chemotherapy but also leaves it unsusceptible to various immunotherapeutic strategies that have been proven successful in other types of cancer. Areas covered: This review highlights the main components of the pancreatic tumor microenvironment, how they cross-talk with each other to generate stroma and promote tumor growth. Additionally, we discuss the most promising treatment targets in the microenvironment whose modulation can be robustly tested in combination with standard of care chemotherapy. Currently, active clinical trials for pancreatic cancer involving components of the microenvironment are also listed. Expert opinion: Although immunotherapeutic approaches involving checkpoint inhibition are being pursued enthusiastically, there is still more work to be done with several other emerging immune targets that could provide therapeutic benefit.
引用
收藏
页码:473 / 482
页数:10
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