Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, No. 88, Italia St, Keshavarz Blvd., Tehran, Iran.
Stem Cell Res Ther. 2022 Sep 5;13(1):459. doi: 10.1186/s13287-022-03145-y.
Over the last 2 decades, induced pluripotent stem cells (iPSCs) have had various potential applications in various medical research areas, from personalized medicine to disease treatment. Different cellular resources are accessible for iPSC generation, such as keratinocytes, skin fibroblasts, and blood or urine cells. However, all these sources are somatic cells, and we must make several changes in a somatic cell's transcriptome and chromatin state to become a pluripotent cell. It has recently been revealed that cancer cells can be a new source of iPSCs production. Cancer cells show similarities with iPSCs in self-renewal capacity, reprogramming potency, and signaling pathways. Although genetic abnormalities and potential tumor formation in cancer cells pose a severe risk, reprogrammed cancer-induced pluripotent stem cells (cancer-iPSCs) indicate that pluripotency can transiently overcome the cancer phenotype. This review discusses whether cancer cells can be a preferable source to generate iPSCs.
在过去的 20 年中,诱导多能干细胞(iPSCs)在从个性化医疗到疾病治疗等各个医学研究领域具有各种潜在应用。可用于生成 iPSC 的不同细胞资源包括角朊细胞、皮肤成纤维细胞以及血液或尿液细胞。然而,所有这些来源都是体细胞,我们必须对体细胞的转录组和染色质状态进行多次改变才能成为多能细胞。最近发现癌细胞可以成为生成 iPSC 的新来源。癌细胞在自我更新能力、重编程能力和信号通路方面与 iPSCs 具有相似性。尽管癌细胞中的遗传异常和潜在肿瘤形成构成了严重的风险,但重编程的癌源性诱导多能干细胞(cancer-iPSCs)表明多能性可以暂时克服癌症表型。本文综述讨论了癌细胞是否可以作为生成 iPSC 的首选来源。