Lipid Metabolic Regulatory Crosstalk Between Cancer Cells and Tumor-Associated Macrophages

被引:2
作者
Liu, Shu [1 ]
Shen, Ying Ying [1 ]
Yin, Li Yang [1 ]
Liu, Jianghua [2 ,4 ]
Zu, Xuyu [1 ,3 ]
机构
[1] Univ South China, Affiliated Hosp 1, Canc Res Inst, Hengyang Med Sch, Hengyang, Hunan, Peoples R China
[2] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Metab & Endocrinol, Hengyang, Hunan, Peoples R China
[3] Univ South China, Affiliated Hosp 1, Canc Res Inst, Hengyang Med Sch, 69,Chuanshan Ave, Hengyang 421001, Hunan, Peoples R China
[4] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Metab & Endocrinol, 69,Chuanshan Ave, Hengyang 421001, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
tumor-associated macrophages; cancer cells; lipid metabolism; targeting therapy; ACID-BINDING PROTEIN; BREAST-CANCER; M2; MACROPHAGES; EXPRESSION; CHOLESTEROL; INHIBITION; GROWTH; MICROENVIRONMENT; 5-LIPOXYGENASE; ACCUMULATION;
D O I
10.1089/dna.2023.0071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the tumor microenvironment, tumor-associated macrophages (TAMs) are one of the most abundant cell populations, playing key roles in tumorigenesis, chemoresistance, immune evasion, and metastasis. There is an important interaction between TAMs and cancer cells: on the one hand, tumors control the function of infiltrating macrophages, contributing to reprogramming of TAMs, and on the other hand, TAMs affect the growth of cancer cells. This review focuses on lipid metabolism changes in the complex relationship between cancer cells and TAMs. We discuss how lipid metabolism in cancer cells affects macrophage phenotypic and metabolic changes and, subsequently, how altered lipid metabolism of TAMs influences tumor progression. Identifying the metabolic changes that influence the complex interaction between tumor cells and TAMs is also an important step in exploring new therapeutic approaches that target metabolic reprogramming of immune cells to enhance their tumoricidal potential and bypass therapy resistance. Our work may provide new targets for antitumor therapies.
引用
收藏
页码:445 / 455
页数:11
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