Fujii Masayuki, Sato Toshiro
Department of Gastroenterology, School of Medicine, Keio University Tokyo, Japan.
Front Genet. 2014 Jun 5;5:169. doi: 10.3389/fgene.2014.00169. eCollection 2014.
Recent advance of sequencing technology has revealed genetic alterations in colorectal cancer (CRC). The biological function of recurrently mutated genes has been intensively investigated through mouse genetic models and CRC cell lines. Although these experimental models may not fully reflect biological traits of human intestinal epithelium, they provided insights into the understanding of intestinal stem cell self-renewal, leading to the development of novel human intestinal organoid culture system. Intestinal organoid culture enabled to expand normal or tumor epithelial cells in vitro retaining their stem cell self-renewal and multiple differentiation. Gene manipulation of these cultured cells may provide an attractive tool for investigating genetic events involved in colorectal carcinogenesis.
测序技术的最新进展揭示了结直肠癌(CRC)中的基因改变。通过小鼠遗传模型和CRC细胞系,对反复突变基因的生物学功能进行了深入研究。尽管这些实验模型可能无法完全反映人类肠道上皮的生物学特性,但它们为理解肠道干细胞自我更新提供了见解,从而推动了新型人类肠道类器官培养系统的发展。肠道类器官培养能够在体外扩增正常或肿瘤上皮细胞,同时保留其干细胞自我更新和多种分化能力。对这些培养细胞进行基因操作可能为研究结直肠癌发生过程中的遗传事件提供一个有吸引力的工具。