Cook Cody C, Higuchi Masahiro
Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Biochim Biophys Acta. 2012 May;1820(5):652-62. doi: 10.1016/j.bbagen.2011.08.017. Epub 2011 Sep 2.
In only months-to-years a primary cancer can progress to an advanced phenotype that is metastatic and resistant to clinical treatments. As early as the 1900s, it was discovered that the progression of a cancer to the advanced phenotype is often associated with a shift in the metabolic profile of the disease from a state of respiration to anaerobic fermentation - a phenomenon denoted as the Warburg Effect.
Reports in the literature strongly suggest that the Warburg Effect is generated as a response to a loss in the integrity of the sequence and/or copy number of the mitochondrial genome content within a cancer.
Multiple studies regarding the progression of cancer indicate that mutation, and/or, a flux in the copy number, of the mitochondrial genome content can support the early development of a cancer, until; the mutational load and/or the reduction-to-depletion of the copy number of the mitochondrial genome content induces the progression of the disease to an advanced phenotype.
Collectively, evidence has revealed that the human cell has incorporated the mitochondrial genome content into a cellular mechanism that, when pathologically actuated, can de(un)differentiate a cancer from the parental tissue of origin into an autonomous disease that disrupts the hierarchical structure-and-function of the human body. This article is part of a Special Issue entitled: Biochemistry of Mitochondria.
在短短数月至数年时间里,原发性癌症可发展为具有转移能力且对临床治疗产生抗性的晚期表型。早在20世纪初就已发现,癌症进展至晚期表型通常与疾病代谢特征从呼吸状态转变为无氧发酵有关——这一现象被称为瓦伯格效应。
文献报道有力地表明,瓦伯格效应是癌症中线粒体基因组内容序列完整性和/或拷贝数缺失的一种反应。
多项关于癌症进展的研究表明,线粒体基因组内容的突变和/或拷贝数变化可支持癌症的早期发展,直到线粒体基因组内容的突变负荷和/或拷贝数减少至耗尽促使疾病进展为晚期表型。
总体而言,证据表明人类细胞已将线粒体基因组内容纳入一种细胞机制,当该机制被病理激活时,可使癌症从其起源的亲代组织中去(未)分化,成为一种破坏人体层次结构和功能的自主性疾病。本文是名为《线粒体生物化学》特刊的一部分。