The poorly immunogenic tumor microenvironment of pancreatic cancer: the impact of radiation therapy, and strategies targeting resistance

被引:3
|
作者
Hughes, Robert [1 ]
Snook, Adam E. [2 ,3 ,4 ]
Mueller, Adam C. [1 ]
机构
[1] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Pharmacol & Expt Therapeut, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
关键词
immunotherapy; lymphoid cells; myeloid cells; pancreatic cancer; PDAC; radiation therapy; SBRT; tumor microenvironment; REGULATORY T-CELLS; DUCTAL ADENOCARCINOMA; SUPPRESSOR-CELLS; NEOADJUVANT CHEMORADIOTHERAPY; HYPOXIC CORE; MURINE MODEL; IMMUNOTHERAPY; IMMUNITY; SURVIVAL; RADIOTHERAPY;
D O I
10.2217/imt-2022-0046
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pancreatic cancer is one of the most lethal cancers, due to its uniquely aggressive behavior and resistance to therapy. The tumor microenvironment of pancreatic cancer is immunosuppressive, and attempts at utilizing immunotherapies have been unsuccessful. Radiation therapy (RT) results in immune activation and antigen presentation in other cancers, but in pancreatic cancer has had limited success in stimulating immune responses. RT activates common pathways of fibrosis and chronic inflammation seen in pancreatic cancer, resulting in immune suppression. Here we describe the pancreatic tumor microenvironment with regard to fibrosis, myeloid and lymphoid cells, and the impact of RT. We also describe strategies of targeting these pathways that have promise to improve outcomes by harnessing the cytotoxic and immune-activating aspects of RT.
引用
收藏
页码:1393 / 1405
页数:13
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