Metabolic reprogramming in cervical cancer and metabolomics perspectives

被引:32
|
作者
Li, Boning [1 ]
Sui, Long [1 ,2 ,3 ]
机构
[1] Fudan Univ, Obstet & Gynecol Hosp, Shanghai 200011, Peoples R China
[2] Fudan Univ, Obstet & Gynecol Hosp, Stetr & Gynecol Hosp, Ctr Diag & Treatment Cerv Dis, Shanghai 200011, Peoples R China
[3] Shanghai Key Lab Female Reprod Endocrine Related, Shanghai 200011, Peoples R China
关键词
Cervical cancer; HPV; p53; Metabolomics; Warburg effect; FATTY-ACID OXIDATION; ENERGY-METABOLISM; GLUTAMINASE; EXPRESSION; P53; MACROPHAGES; LIPOGENESIS; INHIBITION; GLYCOLYSIS; CISPLATIN;
D O I
10.1186/s12986-021-00615-7
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Cumulative studies have shown that metabolic reprogramming is a hallmark of malignant tumors. The emergence of technological advances, such as omics studies, has strongly contributed to the knowledge of cancer metabolism. Cervical cancer is among the most common cancers in women worldwide. Because cervical cancer is a virus-associated cancer and can exist in a precancerous state for years, investigations targeting the metabolic phenotypes of cervical cancer will enhance our understanding of the interference of viruses on host cells and the progression of cervical carcinogenesis. The purpose of this review was to illustrate metabolic perturbations in cervical cancer, the role that human papillomavirus (HPV) plays in remodeling cervical cell metabolism and recent approaches toward application of metabolomics in cervical disease research. Cervical cancer displays typical cancer metabolic profiles, including glycolytic switching, high lactate levels, lipid accumulation and abnormal kynurenine/tryptophan levels. HPV, at least in part, contributes to these alterations. Furthermore, emerging metabolomics data provide global information on the metabolic traits of cervical diseases and may aid in the discovery of biomarkers for diagnosis and therapy.
引用
收藏
页数:14
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