Galluzzi L, Kepp O, Tajeddine N, Kroemer G
INSERM, U848, 39 rue C. Desmoulins, Villejuif, France.
Oncogene. 2008 Aug 7;27(34):4633-5. doi: 10.1038/onc.2008.114. Epub 2008 May 12.
Unlike mitochondria from most normal tissues, cancer cell mitochondria demonstrate an association between the glycolytic enzyme hexokinase (HK) and the voltage-dependent anion channel (VDAC). This provides a therapeutic opportunity, as the association appears to protect tumor cells from mitochondrial outer membrane permeabilization (MOMP), an event that marks the point of no return in multiple pathways leading to cell death. In this issue of Oncogene, the plant hormone methyl jasmonate (MJ) is shown to disrupt the interaction between human HK and VDAC, causing the inhibition of glycolysis and the induction of MOMP. MJ has already been shown to have selective anticancer activity in preclinical studies, and this finding may stimulate the development of a novel class of small anticancer compounds that inhibit the HK-VDAC interaction.
与大多数正常组织的线粒体不同,癌细胞线粒体显示出糖酵解酶己糖激酶(HK)与电压依赖性阴离子通道(VDAC)之间存在关联。这提供了一个治疗机会,因为这种关联似乎能保护肿瘤细胞免受线粒体外膜通透性改变(MOMP)的影响,而MOMP是导致细胞死亡的多种途径中不可逆转的标志。在本期《癌基因》杂志中,植物激素茉莉酸甲酯(MJ)被证明能破坏人HK与VDAC之间的相互作用,从而抑制糖酵解并诱导MOMP。在临床前研究中,MJ已被证明具有选择性抗癌活性,这一发现可能会推动一类新型小分子抗癌化合物的开发,这类化合物可抑制HK-VDAC相互作用。