Links between cancer metabolism and cisplatin resistance

被引:67
作者
Cocetta, Veronica [1 ]
Ragazzi, Eugenio [1 ]
Montopoli, Monica [1 ,2 ]
机构
[1] Univ Padua, Dept Pharmaceut & Pharmacol Sci, Padua, Italy
[2] VIMM Veneto Inst Mol Med, Padua, Italy
关键词
FATTY-ACID SYNTHASE; PYRUVATE-KINASE M2; PENTOSE-PHOSPHATE PATHWAY; X(C)(-) CYSTINE/GLUTAMATE ANTIPORTER; CITRATE LYASE EXPRESSION; TRIGLYCERIDE LIPASE ATGL; SQUAMOUS-CELL CARCINOMA; ADVANCED BLADDER-CANCER; SEROUS OVARIAN-CANCER; GLUTAMINE-METABOLISM;
D O I
10.1016/bs.ircmb.2020.01.005
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
Cisplatin is one of the most potent and widely used chemotherapeutic agent in the treatment of several solid tumors, despite the high toxicity and the frequent relapse of patients due to the onset of drug resistance. Resistance to chemotherapeutic agents, either intrinsic or acquired, is currently one of the major problems in oncology. Thus, understanding the biology of chemoresistance is fundamental in order to overcome this challenge and to improve the survival rate of patients. Studies over the last 30 decades have underlined how resistance is a multifactorial phenomenon not yet completely understood. Recently, tumor metabolism has gained a lot of interest in the context of chemoresistance; accumulating evidence suggests that the rearrangements of the principal metabolic pathways within cells, contributes to the sensitivity of tumor to the drug treatment. In this review, the principal metabolic alterations associated with cisplatin resistance are highlighted. Improving the knowledge of the influence of metabolism on cisplatin response is fundamental to identify new possible metabolic targets useful for combinatory treatments, in order to overcome cisplatin resistance.
引用
收藏
页码:107 / 164
页数:58
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