1. Barts and the London School of Medicine and Dentistry, Greater London, E1 2AD, United Kingdom ; 2. Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
2. Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
Int J Med Sci. 2015 Jan 20;12(3):201-13. doi: 10.7150/ijms.11047. eCollection 2015.
In the last five years, IDH1 mutations in human malignancies have significantly shaped the diagnosis and management of cancer patients. Ongoing intense research efforts continue to alter our understanding of the role of the IDH1 mutation in tumor formation. Currently, evidence suggests the IDH1 mutation to be an early event in tumorigenesis with multiple downstream oncogenic consequences including maintenance of a hypermethylator phenotype, alterations in HIF signalling, and disruption of collagen maturation contributing to a cancer-promoting extracellular matrix. The most recent reports elucidating these mechanisms is described in this review with an emphasis on the pathogenesis of the IDH1 mutation in glioma. Conflicting findings from various studies are discussed, in order to highlight areas warranting further research. Finally, the latest progress in developing novel therapies against the IDH1 mutation is presented, including recent findings from ongoing phase 1 clinical trials and the exciting prospect of vaccine immunotherapy targeting the IDH1 mutant protein.
在过去的五年中,IDH1 突变在人类恶性肿瘤中的作用极大地改变了癌症患者的诊断和治疗方式。目前,仍在进行大量的研究工作,这些工作不断改变我们对 IDH1 突变在肿瘤形成中作用的认识。目前有证据表明,IDH1 突变是肿瘤发生的早期事件,具有多种下游致癌后果,包括维持高甲基化表型、改变 HIF 信号转导以及破坏胶原成熟,从而促进有利于癌症的细胞外基质。本综述重点阐述了 IDH1 突变在神经胶质瘤中的发病机制,描述了这些机制的最新研究进展。同时讨论了来自不同研究的相互矛盾的结果,以突出需要进一步研究的领域。最后,本文还介绍了针对 IDH1 突变的新型治疗方法的最新进展,包括正在进行的 1 期临床试验的最新发现以及针对 IDH1 突变蛋白的疫苗免疫治疗的令人兴奋的前景。