z-logo
open-access-imgOpen Access
Dual roles of myeloid‑derived suppressor cells induced by Toll‑like receptor signaling in cancer (Review)
Author(s) -
Hongyue Zhou,
Mengyu Jiang,
Hongyan Yuan,
Weihua Ni,
Guixiang Tai
Publication year - 2020
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2020.12410
Subject(s) - myeloid derived suppressor cell , immunotherapy , cancer research , tumor microenvironment , immunosuppression , cancer immunotherapy , cancer , toll like receptor , immune system , immunology , biology , oncogene , signal transduction , myeloid , suppressor , cell cycle , innate immune system , microbiology and biotechnology , genetics
Myeloid-derived suppressor cells (MDSCs) are one of the major components of the tumor microenvironment (TME), and are the main mediators of tumor-induced immunosuppression. Recent studies have reported that the survival, differentiation and immunosuppressive activity of MDSCs are affected by the Toll-like receptor (TLR) signaling pathway. However, the regulatory effect of TLR signaling on MDSCs remains controversial. TLR-induced MDSC can acquire different immunosuppressive activities to influence the immune response that can be either beneficial or detrimental to cancer immunotherapy. The present review summarizes the effects of TLR signals on the number, phenotype and inhibitory activity of MDSCs, and their role in cancer immunotherapy, which cannot be ignored if effective cancer immunotherapies are to be developed for the immunosuppression of the TME.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom