Donada A, Basso-Valentina F, Arkoun B, Monte-Mor B, Plo I, Raslova H
INSERM, UMR1287, Université Paris Sud, Université Paris Saclay, Gustave Roussy, Equipe Labellisée LNCC, Villejuif, France.
Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
Stem Cell Res. 2020 Dec;49:102060. doi: 10.1016/j.scr.2020.102060. Epub 2020 Oct 24.
The derivation of human pluripotent stem cell (iPSC) lines by in vitro reprogramming of somatic cells revolutionized research: iPSCs have been used for disease modeling, drug screening and regenerative medicine for many disorders, especially when combined with cutting-edge genome editing technologies. In hematology, malignant transformation is often a multi-step process, that starts with either germline or acquired genetic alteration, followed by progressive acquisition of mutations combined with the selection of one or more pre-existing clones. iPSCs are an excellent model to study the cooperation between different genetic alterations and to test relevant therapeutic drugs. In this review, we will describe the use of iPSCs for pathophysiological studies and drug testing in inherited and acquired hematological malignancies.
通过体细胞的体外重编程来获得人多能干细胞(iPSC)系,这一技术给研究带来了革命性的变化:iPSC已被用于多种疾病的疾病建模、药物筛选和再生医学,尤其是与前沿的基因组编辑技术相结合时。在血液学中,恶性转化通常是一个多步骤过程,始于种系或获得性基因改变,随后逐渐获得突变并伴随着一个或多个预先存在的克隆的选择。iPSC是研究不同基因改变之间协同作用以及测试相关治疗药物的理想模型。在这篇综述中,我们将描述iPSC在遗传性和获得性血液系统恶性肿瘤的病理生理学研究和药物测试中的应用。