Metabolic synthetic lethality in cancer therapy

被引:50
作者
Zecchini, Vincent [1 ]
Frezza, Christian [1 ]
机构
[1] Univ Cambridge, MRC, Hutchison MRC Res Ctr, Canc Unit, Cambridge CB2 0XZ, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2017年 / 1858卷 / 08期
基金
英国医学研究理事会;
关键词
RENAL-CELL CARCINOMA; FUMARATE-HYDRATASE; SUCCINATE-DEHYDROGENASE; GERMLINE MUTATIONS; PYRUVATE CARBOXYLATION; SDH MUTATIONS; METFORMIN; INHIBITION; FH; PROLINE;
D O I
10.1016/j.bbabio.2016.12.003
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
Our understanding of cancer has recently seen a major paradigm shift resulting in it being viewed as a metabolic disorder, and altered cellular metabolism being recognised as a hallmark of cancer. This concept was spurred by the findings that the oncogenic mutations driving tumorigenesis induce a reprogramming of cancer cell metabolism that is required for unrestrained growth and proliferation. The recent discovery that mutations in key mitochondrial enzymes play a causal role in tumorigenesis suggested that dysregulation of metabolism could also be a driver of tumorigenesis. These mutations induce profound adaptive metabolic alterations that are a prerequisite for the survival of the mutated cells. Because these metabolic events are specific to cancer cells, they offer an opportunity to develop new therapies that specifically target tumour cells without affecting healthy tissue. Here, we will describe recent developments in metabolism-based cancer therapy, in particular focusing on the concept of metabolic synthetic lethality. This article is part of a Special Issue entitled Mitochondria in Cancer, edited by Giuseppe Gasparre, Rodrigue Rossignol and Pierre Sonveaux. (C) 2016 Elsevier B.V. All fights reserved.
引用
收藏
页码:723 / 731
页数:9
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