| Literature DB >> 33458695 |
Ting Li1, Xinyuan Li1, Ali Zamani1, Wei Wang1, Chin-Nien Lee1, Mingyue Li1, George Luo1, Emily Eiler1, Honghong Sun1, Sankar Ghosh2, Jian Jin3,4, Ramachandran Murali5, Qingguo Ruan6, Weiyun Shi6, Youhai H Chen7.
Abstract
Immunotherapy that targets lymphoid cell checkpoints holds great promise for curing cancer. However, a majority of cancer patients do not respond to this form of therapy. In addition to lymphoid cells, myeloid cells play essential roles in controlling immunity to cancer. Whether myeloid checkpoints exist that can be targeted to treat cancer is not well established. Here we show that c-Rel, a member of the nuclear factor (NF)-B family, specified the generation of myeloid-derived suppressor cells (MDSCs) by selectively turning on pro-tumoral genes while switching off anti-tumoral genes through a c-Rel enhanceosome. c-Rel deficiency in myeloid cells markedly inhibited cancer growth in mice, and pharmaceutical inhibition of c-Rel had the same effect. Combination therapy that blocked both c-Rel and the lymphoid checkpoint protein PD1 was more effective in treating cancer than blocking either alone. Thus, c-Rel is a myeloid checkpoint that can be targeted for treating cancer.Entities:
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Year: 2020 PMID: 33458695 PMCID: PMC7808269 DOI: 10.1038/s43018-020-0061-3
Source DB: PubMed Journal: Nat Cancer ISSN: 2662-1347