Targeting Energy Metabolism in Cancer Treatment

被引:16
|
作者
Kubik, Joanna [1 ]
Humeniuk, Ewelina [1 ]
Adamczuk, Grzegorz [1 ]
Madej-Czerwonka, Barbara [2 ]
Korga-Plewko, Agnieszka [1 ]
机构
[1] Med Univ Lublin, Fac Pharm, Independent Med Biol Unit, PL-20093 Lublin, Poland
[2] Med Univ Lublin, Dept Human Anat, Fac Med, PL-20090 Lublin, Poland
关键词
cancer metabolism; cancer treatment; glycolysis; oxidative phosphorylation; FATTY-ACID SYNTHASE; PENTOSE-PHOSPHATE PATHWAY; ACUTE MYELOID-LEUKEMIA; PYRUVATE-KINASE M2; ADENINE-NUCLEOTIDE TRANSLOCASE; KIDNEY-TYPE GLUTAMINASE; BCL-2 FAMILY PROTEINS; CELL-CYCLE ARREST; LACTATE-DEHYDROGENASE; IN-VITRO;
D O I
10.3390/ijms23105572
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
Cancer is the second most common cause of death worldwide after cardiovascular diseases. The development of molecular and biochemical techniques has expanded the knowledge of changes occurring in specific metabolic pathways of cancer cells. Increased aerobic glycolysis, the promotion of anaplerotic responses, and especially the dependence of cells on glutamine and fatty acid metabolism have become subjects of study. Despite many cancer treatment strategies, many patients with neoplastic diseases cannot be completely cured due to the development of resistance in cancer cells to currently used therapeutic approaches. It is now becoming a priority to develop new treatment strategies that are highly effective and have few side effects. In this review, we present the current knowledge of the enzymes involved in the different steps of glycolysis, the Krebs cycle, and the pentose phosphate pathway, and possible targeted therapies. The review also focuses on presenting the differences between cancer cells and normal cells in terms of metabolic phenotype. Knowledge of cancer cell metabolism is constantly evolving, and further research is needed to develop new strategies for anti-cancer therapies.
引用
收藏
页数:39
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