| Literature DB >> 26966191 |
Stephanie C Casey1, Ling Tong1, Yulin Li1, Rachel Do1, Susanne Walz2, Kelly N Fitzgerald1, Arvin M Gouw1, Virginie Baylot1, Ines Gütgemann3, Martin Eilers4, Dean W Felsher5.
Abstract
The MYC oncogene codes for a transcription factor that is overexpressed in many human cancers. Here we show that MYC regulates the expression of two immune checkpoint proteins on the tumor cell surface: the innate immune regulator CD47 (cluster of differentiation 47) and the adaptive immune checkpoint PD-L1 (programmed death-ligand 1). Suppression of MYC in mouse tumors and human tumor cells caused a reduction in the levels of CD47 and PD-L1 messenger RNA and protein. MYC was found to bind directly to the promoters of the Cd47 and Pd-l1 genes. MYC inactivation in mouse tumors down-regulated CD47 and PD-L1 expression and enhanced the antitumor immune response. In contrast, when MYC was inactivated in tumors with enforced expression of CD47 or PD-L1, the immune response was suppressed, and tumors continued to grow. Thus, MYC appears to initiate and maintain tumorigenesis, in part, through the modulation of immune regulatory molecules.Entities:
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Year: 2016 PMID: 26966191 PMCID: PMC4940030 DOI: 10.1126/science.aac9935
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728