Center for iPS Cell Research and Application, Kyoto University.
Division of Stem Cell Pathology, Center for Experimental Medicine and Systems Biology, Institute of Medical Science, the University of Tokyo.
Proc Jpn Acad Ser B Phys Biol Sci. 2018;94(6):235-247. doi: 10.2183/pjab.94.016.
There is increasing evidence that cancer cells acquire epigenetic abnormalities as well as genetic mutations during cancer initiation, maintenance, and progression. However, the role of epigenetic regulation in cancer development, especially at the organismal level, remains to be elucidated. Here, we describe the causative role of epigenetic abnormalities in cancer, referring to our in vivo studies using induced pluripotent stem cell technology. We first summarize epigenetic reorganization during cellular reprogramming and introduce our in vivo reprogramming system for investigating the impact of dedifferentiation-driven epigenetic disruption in cancer development. Accordingly, we propose that particular types of cancer, in which causative mutations are not often detectable, such as pediatric cancers like Wilms' tumor, may develop mainly through alterations in epigenetic regulation triggered by dedifferentiation. Finally, we discuss issues that still remain to be resolved, and propose possible future applications of in vivo reprogramming to study cancer and other biological phenomena including organismal aging.
越来越多的证据表明,癌细胞在癌症的起始、维持和进展过程中会获得表观遗传异常和基因突变。然而,表观遗传调控在癌症发展中的作用,特别是在机体水平上,仍有待阐明。在这里,我们描述了表观遗传异常在癌症中的因果作用,参考了我们使用诱导多能干细胞技术进行的体内研究。我们首先总结了细胞重编程过程中的表观遗传重组,并介绍了我们的体内重编程系统,用于研究去分化驱动的表观遗传破坏对癌症发展的影响。因此,我们提出,在某些类型的癌症中,如儿童癌症如肾母细胞瘤,由于常见的致癌突变不易检测到,可能主要通过去分化触发的表观遗传调控的改变而发展。最后,我们讨论了仍有待解决的问题,并提出了体内重编程在研究癌症和其他生物学现象(包括机体衰老)方面的可能未来应用。