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Tumor-associated fibrosis as a regulator of tumor immunity and response to immunotherapy

期刊

CANCER IMMUNOLOGY IMMUNOTHERAPY
卷 66, 期 8, 页码 1037-1048

出版社

SPRINGER
DOI: 10.1007/s00262-017-2003-1

关键词

Fibrosis; Extracellular matrix; Tumor microenvironment; Tumor immunity; Pancreas cancer; Regulatory myeloid suppressor cells

资金

  1. NCI NIH HHS [R01 CA203890, P30 CA091842, R01 CA177670, F99 CA223043, P50 CA196510] Funding Source: Medline

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Tumor-associated fibrosis is characterized by unchecked pro-fibrotic and pro-inflammatory signaling. The components of fibrosis including significant numbers of cancer-associated fibroblasts, dense collagen deposition, and extracellular matrix stiffness, are well appreciated regulators of tumor progression but may also be critical regulators of immune surveillance. While this suggests that the efficacy of immunotherapy may be limited in highly fibrotic cancers like pancreas, it also suggests a therapeutic opportunity to target fibrosis in these tumor types to reawaken anti-tumor immunity. This review discusses the mechanisms by which fibrosis might subvert tumor immunity and how to overcome these mechanisms.

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