Src: coordinating metabolism in cancer

被引:53
作者
Pelaz, Sara G. [1 ]
Tabernero, Arantxa [1 ]
机构
[1] Univ Salamanca, Inst Neurociencias Castilla & Leon INCYL, Dept Bioquim & Biol Mol, Inst Invest Biomed Salamanca IBSAL, Calle Pintor Fernando Gallego 1, Salamanca 37007, Spain
关键词
ROUS-SARCOMA-VIRUS; DEPENDENT TYROSINE PHOSPHORYLATION; C-SRC; FAMILY KINASES; GLUCOSE-TRANSPORTER; GROWTH-FACTOR; OXIDATIVE-PHOSPHORYLATION; ONCOGENIC PROPERTIES; PHOSPHATASE-ACTIVITY; MEDIATED ACTIVATION;
D O I
10.1038/s41388-022-02487-4
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
Metabolism must be tightly regulated to fulfil the dynamic requirements of cancer cells during proliferation, migration, stemness and differentiation. Src is a node of several signals involved in many of these biological processes, and it is also an important regulator of cell metabolism. Glucose uptake, glycolysis, the pentose-phosphate pathway and oxidative phosphorylation are among the metabolic pathways that can be regulated by Src. Therefore, this oncoprotein is in an excellent position to coordinate and finely tune cell metabolism to fuel the different cancer cell activities. Here, we provide an up-to-date summary of recent progress made in determining the role of Src in glucose metabolism as well as the link of this role with cancer cell metabolic plasticity and tumour progression. We also discuss the opportunities and challenges facing this field.
引用
收藏
页码:4917 / 4928
页数:12
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