Nguyen Tran Ngoc Anh, Lai Hong-Toan, Fernandes Romain, Dall'Olio Filippo G, Blériot Camille, Ha-Duong Tap, Brenner Catherine
Aspects métaboliques et systémiques de l'oncogénèse pour de nouvelles approches thérapeutiques, CNRS, Institut Gustave Roussy, Université Paris- Saclay, Villejuif, France.
BioCIS, CNRS, Université Paris-Saclay, Orsay, 91400, France.
Cell Commun Signal. 2025 Jun 4;23(1):264. doi: 10.1186/s12964-025-02272-2.
Apoptosis-inducing factor (AIF), a mitochondrial NAD(P)H-dependent oxidoreductase, was initially studied as a cell death inducer in a process later named parthanatos. However, it has been revealed that AIF also participates in mitochondrial bioenergetics through interaction with its partner coiled-coil-helix-coiled-coil-helix domain containing 4 (CHCHD4) and involvement in mitochondrial protein import. These dual roles place AIF between pro-survival and pro-death cell fate decisions. In this review, we first describe the structure and the dual functions of AIF, highlighting its structure-function relationships. We then report previously identified AIFM1 mutations and their clinical phenotypes. Finally, we discuss the relevance of AIF in cancer and the potential of targeting this protein for the treatment of cancer.
凋亡诱导因子(AIF)是一种线粒体烟酰胺腺嘌呤二核苷酸(磷酸)依赖性氧化还原酶,最初被作为一种细胞死亡诱导因子进行研究,该过程后来被命名为细胞焦亡。然而,现已发现AIF还通过与其伴侣卷曲螺旋-螺旋-卷曲螺旋-螺旋结构域包含蛋白4(CHCHD4)相互作用参与线粒体生物能量学,并参与线粒体蛋白导入。这些双重作用使AIF处于细胞存活和细胞死亡命运决定之间。在本综述中,我们首先描述AIF的结构和双重功能,突出其结构-功能关系。然后我们报告先前鉴定的AIFM1突变及其临床表型。最后,我们讨论AIF在癌症中的相关性以及靶向该蛋白治疗癌症的潜力。