INSERM U917, Microenvironnement et Cancer, Rennes, France; Université de Rennes 1, Rennes, France.
INSERM U917, Microenvironnement et Cancer, Rennes, France; Université de Rennes 1, Rennes, France; Etablissement Français du Sang, Rennes, France.
Cancer Lett. 2014 Apr 1;345(1):1-16. doi: 10.1016/j.canlet.2013.11.016. Epub 2013 Dec 11.
ING genes (ING1-5) were identified has tumor suppressor genes. ING proteins are characterized as Type II TSGs since they are involved in the control of cell proliferation, apoptosis and senescence. They may also function as Type I TSGs since they are also involved in DNA replication and repair. Most studies have reported that they are frequently lost in human tumors and epigenetic mechanisms or misregulation of their transcription may be involved. Recently, studies have described that this loss may be caused by microRNA inhibition. Here, we summarize the current knowledge on ING functions, their involvement in tumor suppression and, in order to give a full assessment of the current knowledge, we review all the studies that have examined ING status in human cancers.
ING 基因(ING1-5)被鉴定为肿瘤抑制基因。ING 蛋白的特点是 II 型 TSGs,因为它们参与控制细胞增殖、凋亡和衰老。它们也可能作为 I 型 TSGs 发挥作用,因为它们也参与 DNA 复制和修复。大多数研究报告称,它们在人类肿瘤中经常丢失,并且可能涉及表观遗传机制或转录的失调。最近的研究表明,这种丢失可能是由 microRNA 抑制引起的。在这里,我们总结了 ING 功能的最新知识,它们在肿瘤抑制中的作用,为了全面评估目前的知识,我们回顾了所有研究 ING 在人类癌症中的状态的研究。