Metabolic reprogramming in colorectal cancer: regulatory networks and therapy

被引:21
作者
Zhang, Jieping [1 ,2 ]
Zou, Shaomin [1 ,2 ]
Fang, Lekun [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Gen Surg, Guangdong Prov Key Lab Colorectal & Pelv Floor Dis, 26 Yuanchun Er Heng Rd, Guangzhou 510655, Guangdong, Peoples R China
[2] Guangdong Inst Gastroenterol, Guangzhou 510655, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal cancer; Metabolic reprogramming; Metabolic enzymes; Signal transduction; Targeted therapy; PENTOSE-PHOSPHATE PATHWAY; FATTY-ACID SYNTHASE; PYRUVATE-KINASE M2; COLON-CANCER; AEROBIC GLYCOLYSIS; MALIC ENZYME; TRANSCRIPTIONAL REGULATION; GLUTAMINE-METABOLISM; CELL PROLIFERATION; TUMOR PROGRESSION;
D O I
10.1186/s13578-023-00977-w
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
With high prevalence and mortality, together with metabolic reprogramming, colorectal cancer is a leading cause of cancer-related death. Metabolic reprogramming gives tumors the capacity for long-term cell proliferation, making it a distinguishing feature of cancer. Energy and intermediate metabolites produced by metabolic reprogramming fuel the rapid growth of cancer cells. Aberrant metabolic enzyme-mediated tumor metabolism is regulated at multiple levels. Notably, tumor metabolism is affected by nutrient levels, cell interactions, and transcriptional and posttranscriptional regulation. Understanding the crosstalk between metabolic enzymes and colorectal carcinogenesis factors is particularly important to advance research for targeted cancer therapy strategies via the investigation into the aberrant regulation of metabolic pathways. Hence, the abnormal roles and regulation of metabolic enzymes in recent years are reviewed in this paper, which provides an overview of targeted inhibitors for targeting metabolic enzymes in colorectal cancer that have been identified through tumor research or clinical trials.
引用
收藏
页数:21
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