Metabolic reprogramming and epigenetic modifications on the path to cancer
Метаболическое перепрограммирование и эпигенетические модификации на пути к раку
2021-05-29
SCID: 54.1/6z9zpzaq
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cancer metabolismepigenetic remodelinghistone acetylation and methylationimmune escapemetabolic reprogramming
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Abstract (AI)
Metabolic rewiring and epigenetic remodeling, which are closely linked and reciprocally regulate each other, are among the well-known cancer hallmarks. Recent evidence suggests that many metabolites serve as substrates or cofactors of chromatin-modifying enzymes as a consequence of the translocation or spatial regionalization of enzymes or metabolites. Various metabolic alterations and epigenetic modifications also reportedly drive immune escape or impede immunosurveillance within certain contexts, playing important roles in tumor progression. In this review, we focus on how metabolic reprogramming of tumor cells and immune cells reshapes epigenetic alterations, in particular the acetylation and methylation of histone proteins and DNA. We also discuss other eminent metabolic modifications such as, succinylation, hydroxybutyrylation, and lactylation, and update the current advances in metabolism- and epigenetic modification-based therapeutic prospects in cancer.
Key Findings
1
Metabolic alterations and epigenetic modifications can promote tumor progression by enabling immune escape or impairing immunosurveillance in context-dependent ways.
2
Metabolic rewiring and epigenetic remodeling reciprocally regulate each other and represent interconnected hallmarks of cancer.
3
Metabolites can act as substrates or cofactors for chromatin-modifying enzymes, particularly following enzyme translocation or metabolite spatial compartmentalization.
4
Therapeutic strategies targeting cancer metabolism and epigenetic modifications are emerging as promising prospects for cancer treatment.
5
Tumor-cell and immune-cell metabolism reshapes histone and DNA acetylation and methylation, as well as emerging modifications including succinylation, hydroxybutyrylation, and lactylation.
Research Object
Metabolic reprogramming and epigenetic modifications in tumor cells and immune cells during cancer development
Research Subject
Reciprocal regulation between altered metabolism and epigenetic modifications—including histone and DNA acetylation and methylation, succinylation, hydroxybutyrylation, and lactylation—and their roles in immune escape and tumor progression
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2021-05-29
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