Patient-derived induced pluripotent stem cells for models of cancer and cancer stem cell research

被引:25
|
作者
Chao, Hsiao-Mei [1 ,2 ]
Chern, Edward [1 ]
机构
[1] Natl Taiwan Univ, Dept Biochem Sci & Technol, NiChe Lab Stem Cell & Regenerat Med, Taipei, Taiwan
[2] Taipei Med Univ, Wan Fang Hosp, Dept Pathol, Taipei, Taiwan
关键词
Induced pluripotent stem cells (iPSCs); Cell reprogramming; Tumorigenesis; Cancer stem cell; C VIRUS-INFECTION; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; MESENCHYMAL TRANSITION; COLORECTAL-CANCER; SELF-RENEWAL; IPSC LINE; EXPRESSION; DISEASE; TUMORIGENESIS;
D O I
10.1016/j.jfma.2018.06.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Induced pluripotent stem cells (iPSCs) are embryonic stem cell-like cells reprogrammed from somatic cells by four transcription factors, OCT4, SOX2, KLF4 and c-MYC. iPSCs derived from cancer cells (cancer-iPSCs) could be a novel strategy for studying cancer. During cancer cell reprogramming, the epigenetic status of the cancer cell may be altered, such that it acquires stemness and pluripotency. The cellular behavior of the reprogrammed cells exhibits dynamic changes during the different stages of reprogramming. The cells may acquire the properties of cancer stem cells (CSCs) during the process of reprogramming, and lose their carcinogenic properties during reprogramming into a cancer-iPSCs. Differentiation of cancer-iPSCs by teratoma formation or organoid culturing could mimic the process of tumorigenesis. Some of the molecular mechanisms associated with cancer progression could be elucidated using the cancer-iPSC model. Furthermore, cancer-iPSCs could be expanded in culture system or bioreactors, and serve as cell sources for research, and as personal disease models for therapy and drug screening. This article introduces cancer studies that used the cell reprogramming strategy. Copyright (C) 2018, Formosan Medical Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:1046 / 1057
页数:12
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