Tyrosine metabolic reprogramming coordinated with the tricarboxylic acid cycle to drive glioma immune evasion by regulating PD‐L1 expression
نویسندگان
چکیده
Due to the existence of blood–brain barrier in glioma, traditional drug therapy has a poor therapeutic outcome. Emerging immunotherapy been shown have satisfactory effects solid tumors, and it is clinically instructive explore possibility glioma. We performed retrospective analysis RNA-seq data clinical information 1027 glioma patients, utilizing machine learning relationship between tyrosine metabolizing enzymes characteristics. In addition, we also assessed role immune microenvironment including infiltration evasion. Highly expressed 4-hydroxyphenylpyruvate dioxygenase, homogentisate 1,2-dioxygenase, fumarylacetoacetate hydrolase not only promote malignant phenotype but are closely related prognosis. The expression could distinguish malignancy degree More importantly, regulate adaptive process Mechanistically, multiple metabolic remodel fumarate metabolism, α-ketoglutarate production, induce programmed death-ligand 1 expression, help evade surveillance. Our suggest that subclass driven by metabolism provides promising targets for
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ژورنال
عنوان ژورنال: Ibrain
سال: 2023
ISSN: ['2769-2795', '2313-1934']
DOI: https://doi.org/10.1002/ibra.12107