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Advances and Challenges on Cancer Cells Reprogramming Using Induced Pluripotent Stem Cells Technologies

机译:利用诱导多能干细胞技术对癌细胞进行重编程的进展和挑战

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摘要

Cancer cells transformation into a normal state or into a cancer cell population which is less tumorigenic than the initial one is a challenge that has been discussed during last decades and it is still far to be solved. Due to the highly heterogeneous nature of cancer cells, such transformation involves many genetic and epigenetic factors which are specific for each type of tumor. Different methods of cancer cells reprogramming have been established and can represent a possibility to obtain less tumorigenic or even normal cells. These methods are quite complex, thus a simple and efficient method of reprogramming is still required. As soon as induced pluripotent stem cells (iPSC) technology, which allowed to reprogram terminally differentiated cells into embryonic stem cells (ESC)-like, was developed, the method strongly attracted the attention of researches, opening new perspectives for stem cell (SC) personalized therapies and offering a powerful in vitro model for drug screening. This technology is also used to reprogram cancer cells, thus providing a modern platform to study cancer-related genes and the interaction between these genes and the cell environment before and after reprogramming, in order to elucidate the mechanisms of cancer initiation and progression. The present review summarizes recent advances on cancer cells reprogramming using iPSC technology and shows the progress achieved in such field.
机译:癌细胞转变成正常状态或致癌性低于最初的癌细胞群体是近几十年来一直在讨论的一个挑战,并且仍然有待解决。由于癌细胞的高度异质性,这种转化涉及许多对每种类型的肿瘤都具有特异性的遗传和表观遗传因素。已经建立了癌细胞重编程的不同方法,并且可以代表获得较少致瘤性或什至正常细胞的可能性。这些方法非常复杂,因此仍然需要一种简单而有效的重新编程方法。一旦诱导多能干细胞(iPSC)技术可以将最终分化的细胞重编程为胚胎干细胞(ESC)样,该方法就引起了研究的广泛关注,为干细胞(SC)开辟了新的前景。个性化疗法,并提供强大的体外药物筛选模型。该技术还用于对癌细胞进行重编程,从而提供了一个现代化的平台来研究与癌症相关的基因以及这些基因在重编程之前和之后与细胞环境之间的相互作用,从而阐明了癌症发生和发展的机制。本综述总结了使用iPSC技术进行癌细胞重编程的最新进展,并显示了在该领域所取得的进展。

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