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在培养的人类肠道干细胞中的顺序癌症突变
Jarno Drost1, Richard H van Jaarsveld2, Bas Ponsioen2
11] Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and UMC Utrecht, 3584CT Utrecht, The Netherlands [2] Cancer Genomics Netherlands, UMC Utrecht, 3584CG Utrecht, The Netherlands.
Nature
|April 30, 2015
概括
人类肠道干细胞被基因改造,以研究结直肠癌的发展. 关键癌症基因 (APC,P53,KRAS,SMAD4) 的突变产生了在小鼠中形成侵入性瘤的器官,揭示了癌症进展的洞察力.
科学领域:
- 胃肠病学 胃肠病学
- 在瘤学瘤学.
- 干细胞生物学 干细胞生物学
背景情况:
- 肠道干细胞是结直肠癌的起源.
- 人体肠道干细胞可以培养成稳定的上皮器官有机体.
- 像APC,P53,KRAS和SMAD4这样的关键基因在结直肠癌中经常发生突变.
研究的目的:
- 使用CRISPR/Cas9.9进行人类肠道干细胞的基因改造.
- 调查常见的结直肠癌基因突变在有机体发育和瘤形成中的作用.
- 了解结直肠癌进展的早期事件.
主要方法:
- 利用CRISPR/Cas9用于培养人类肠道干细胞中的向基因编辑.
- 开发的转基因肠道有机体.
- 通过操纵培养基生长因子来选择突变器官.
- 异种移植的突变器官在小鼠中进行瘤形成研究.
主要成果:
- 产生的有机体具有APC,P53,KRAS和SMAD4中的突变.
- 四重突变有机体的生长独立于干细胞的利基因素.
- 突变的有机体耐受P53稳定.
- 异种移植的四重突变物在小鼠中形成了侵入性癌瘤.
- 损失APC和P53诱导了体积,这是瘤进展的标志.
结论:
- 经过基因工程的人体肠道干细胞有机体作为结直肠癌的模型.
- 特定的基因突变驱动瘤的开始和进展.
- 结合APC和P53的损失足以在肠道瘤中启动形积分.
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