Functions and mechanisms of lactylation in carcinogenesis and immunosuppression

被引:18
作者
Su, Jing [1 ,2 ,3 ]
Zheng, Zhuangzhuang [1 ,2 ,3 ]
Bian, Chenbin [1 ,2 ,3 ]
Chang, Sitong [1 ,2 ,3 ]
Bao, Jindian [1 ,2 ,3 ]
Yu, Huiyuan [1 ,2 ,3 ]
Xin, Ying [4 ]
Jiang, Xin [1 ,2 ,3 ]
机构
[1] First Hosp Jilin Univ, Jilin Prov Key Lab Radiat Oncol & Therapy, Changchun, Peoples R China
[2] First Hosp Jilin Univ, Dept Radiat Oncol, Changchun, Peoples R China
[3] Jilin Univ, NHC Key Lab Radiobiol, Sch Publ Hlth, Changchun, Peoples R China
[4] Jilin Univ, Key Lab Pathobiol, Minist Educ, Changchun, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
immunosuppression; lactylation (Kla); metabolic reprogramming; tumor microenvironment (TME); Warburg effect; REGULATORY T-CELLS; LACTIC-ACID; DICHLOROACETATE DCA; GLUCOSE-METABOLISM; TGF-BETA; LACTATE; TUMOR; CANCER; GROWTH; GUT;
D O I
10.3389/fimmu.2023.1253064
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As critical executors regulating many cellular operations, proteins determine whether living activities can be performed in an orderly and efficient manner. Precursor proteins are inert and must be modified posttranslationally to enable a wide range of protein types and functions. Protein posttranslational modifications (PTMs) are well recognized as being directly associated with carcinogenesis and immune modulation and have emerged as important targets for cancer detection and treatment. Lactylation (Kla), a novel PTM associated with cellular metabolism found in a wide range of cells, interacts with both histone and nonhistone proteins. Unlike other epigenetic changes, Kla has been linked to poor tumor prognosis in all current studies. Histone Kla can affect gene expression in tumors and immunological cells, thereby promoting malignancy and immunosuppression. Nonhistone proteins can also regulate tumor progression and treatment resistance through Kla. In this review, we aimed to summarize the role of Kla in the onset and progression of cancers, metabolic reprogramming, immunosuppression, and intestinal flora regulation to identify new molecular targets for cancer therapy and provide a new direction for combined targeted therapy and immunotherapy.
引用
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页数:13
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