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线粒体与癌症。

Mitochondria and cancer.

机构信息

Children's Hospital of Philadelphia, Center for Mitochondrial and Epigenomic Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

Nat Rev Cancer. 2012 Oct;12(10):685-98. doi: 10.1038/nrc3365.


DOI:10.1038/nrc3365
PMID:23001348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4371788/
Abstract

Contrary to conventional wisdom, functional mitochondria are essential for the cancer cell. Although mutations in mitochondrial genes are common in cancer cells, they do not inactivate mitochondrial energy metabolism but rather alter the mitochondrial bioenergetic and biosynthetic state. These states communicate with the nucleus through mitochondrial 'retrograde signalling' to modulate signal transduction pathways, transcriptional circuits and chromatin structure to meet the perceived mitochondrial and nuclear requirements of the cancer cell. Cancer cells then reprogramme adjacent stromal cells to optimize the cancer cell environment. These alterations activate out-of-context programmes that are important in development, stress response, wound healing and nutritional status.

摘要

与传统观点相反,功能线粒体对于癌细胞是必不可少的。尽管线粒体基因的突变在癌细胞中很常见,但它们并没有使线粒体能量代谢失活,而是改变了线粒体的生物能量和生物合成状态。这些状态通过线粒体“逆行信号”与核进行通讯,以调节信号转导途径、转录回路和染色质结构,从而满足癌细胞对线粒体和核的感知需求。然后,癌细胞重新编程相邻的基质细胞,以优化癌细胞的环境。这些改变激活了在发育、应激反应、伤口愈合和营养状态中很重要的脱离上下文的程序。

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本文引用的文献

[1]
IDH1(R132H) mutation increases murine haematopoietic progenitors and alters epigenetics.

Nature. 2012-8-30

[2]
Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development.

Proc Natl Acad Sci U S A. 2012-6-11

[3]
Autophagy and senescence in cancer-associated fibroblasts metabolically supports tumor growth and metastasis via glycolysis and ketone production.

Cell Cycle. 2012-6-15

[4]
Inhibition of α-KG-dependent histone and DNA demethylases by fumarate and succinate that are accumulated in mutations of FH and SDH tumor suppressors.

Genes Dev. 2012-6-7

[5]
A mitochondrial pyruvate carrier required for pyruvate uptake in yeast, Drosophila, and humans.

Science. 2012-5-24

[6]
Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespan.

Oncogene. 2012-5-7

[7]
Regulation of oxidative phosphorylation complex activity: effects of tissue-specific metabolic stress within an allometric series and acute changes in workload.

Am J Physiol Regul Integr Comp Physiol. 2012-2-29

[8]
mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination.

Genes Dev. 2012-2-15

[9]
IDH mutation impairs histone demethylation and results in a block to cell differentiation.

Nature. 2012-2-15

[10]
Transformation by the (R)-enantiomer of 2-hydroxyglutarate linked to EGLN activation.

Nature. 2012-2-15

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