基因敲除
小干扰RNA
核糖核酸
下调和上调
信使核糖核酸
化学
PD-L1
癌细胞
N6-甲基腺苷
细胞
癌症研究
细胞生物学
脱甲基酶
生物
分子生物学
免疫系统
癌症
基因
生物化学
免疫学
甲基转移酶
免疫疗法
甲基化
表观遗传学
遗传学
作者
Nobuhiro Tsuruta,Kazufumi Tsuchihashi,Hirofumi Ohmura,Kyoko Yamaguchi,Mamoru Ito,Hiroshi Ariyama,Hitoshi Kusaba,Koichi Akashi,Eishi Baba
标识
DOI:10.1016/j.bbrc.2020.06.153
摘要
Fat mass and obesity-associated protein (FTO) is an enzyme that demethylates N6-methyladenosine (m6A), the most abundant RNA modifications in a cell. The upregulated expression of FTO promotes the progression of various types of cancer by modulating cell-intrinsic genes which relate to malignant potential. However, the impact of FTO on the expression of immune-checkpoint molecules in the tumor cells, which are important for immune escape, has not been well understood. We examined the relevance of FTO to programmed cell death-ligand 1 (PD-L1) expression in colon cancer cells. HCT-116 cells showed high expression of both FTO and PD-L1 proteins. The knockdown of FTO by small interfering RNA decreased mRNA and protein levels of PD-L1 in HCT-116 cells. To elucidate the underlying mechanism by which FTO regulates the expression of PD-L1, we depleted FTO in HCT-116 in the presence of IFN-γ, which is a major stimulus to upregulate PD-L1 expression. Depletion of FTO reduced PD-L1 expression in an IFN-γ signaling-independent manner. RNA immunoprecipitation assay revealed the m6A modification of the PD-L1 mRNA and the binding of FTO to the PD-L1 mRNA in HCT-116. Taken together, our results indicated that FTO could regulate PD-L1 expression in colon cancer cells and provides new insights into the regulation of PD-L1 expression by RNA modification.
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