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ANT2在癌细胞中的具体作用是什么?

[What is the specific role of ANT2 in cancer cells?].

作者信息

Chevrollier Arnaud, Loiseau Dominique, Stepien Georges

机构信息

Laboratoire d'étude des molécules marquées, Inserm U.484, 58, rue Montalembert, 63005 Clermont-Ferrand, France.

出版信息

Med Sci (Paris). 2005 Feb;21(2):156-61. doi: 10.1051/medsci/2005212156.

Abstract

In the mitochondrial internal membrane, the adenine nucleotide translocator (ANT) carries out the ATP/ADP exchange between cytoplasm and mitochondrial matrix. Three isoforms with different kinetic properties are encoded from three different genes in Human: the muscle specific ANT1 and the ubiquitary ANT3 isoforms export ATP produced by mitochondrial oxidative phosphorylation (OXPHOS). The ANT2 isoform is specifically expressed in proliferative cells with a predominant glycolytic metabolism and is associated with cellular undifferentiation which is a major characteristic in carcinogenesis. Its role would be to import into mitochondria ATP produced by the glycolysis, energy essential to several intramitochondrial functions, particularly to maintenance of the membrane potential (Delta Psi m), conditioning cellular survival and proliferation. The mechanism of regeneration of this Delta Psi m gradient would involve at least three major proteins: the hexokinase II isoform, the ANT2 isoform and the F1 part of the mitochondrial ATP synthase complex. Taking into account this major role of ANT2 in cell proliferation and the very low expression of this isoform in differentiated tissues, this protein or its transcript could be chosen as a target for an anticancer strategy. Furthermore, previous studies showed that molecules of the cisplatin family, used as chemotherapeutic agents, led to the destruction of the mitochondrial membrane potential and thus to cell death. Does the anticancer effect of these molecules result, at least partially, from this mitochondrial aggression? If it is the case, the ANT2 isoform, mainly involved in the generation of this potential by its ATP4-/ADP3- exchange, could be considered as a more specific targeting by an RNA interference approach.

摘要

在线粒体内膜中,腺嘌呤核苷酸转运体(ANT)负责细胞质与线粒体基质之间的ATP/ADP交换。人类的三个不同基因编码了三种具有不同动力学特性的异构体:肌肉特异性的ANT1和普遍存在的ANT3异构体输出线粒体氧化磷酸化(OXPHOS)产生的ATP。ANT2异构体在具有主要糖酵解代谢的增殖细胞中特异性表达,并且与细胞未分化相关,而细胞未分化是致癌作用的一个主要特征。其作用是将糖酵解产生的ATP导入线粒体,这是几种线粒体内功能所必需的能量,特别是维持膜电位(ΔΨm),决定细胞的存活和增殖。这种ΔΨm梯度的再生机制至少涉及三种主要蛋白质:己糖激酶II异构体、ANT2异构体和线粒体ATP合酶复合体的F1部分。考虑到ANT2在细胞增殖中的这一主要作用以及该异构体在分化组织中的极低表达,这种蛋白质或其转录本可被选为抗癌策略的靶点。此外,先前的研究表明,用作化疗药物的顺铂家族分子会导致线粒体膜电位的破坏,从而导致细胞死亡。这些分子的抗癌作用至少部分是由这种线粒体攻击导致的吗?如果是这样,主要通过其ATP4-/ADP3-交换参与这种电位产生的ANT2异构体,可以通过RNA干扰方法被视为更特异性的靶向目标。

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