Reprogramming cancer cells: overview & current progress

被引:13
|
作者
Lim, Kian Lam [1 ]
Teoh, Hoon Koon [1 ,2 ]
Choong, Pei Feng [1 ,2 ]
Teh, Hui Xin [1 ]
Cheong, Soon Keng [1 ]
Kamarul, Tunku [3 ]
机构
[1] Univ Tunku Abdul Rahman, Fac Med & Hlth Sci, Sungai Long 43000, Selangor, Malaysia
[2] Univ Kebangsaan Malaysia, PPUKM MAKNA Canc Ctr, Med Ctr, Cheras, Malaysia
[3] Univ Malaya, Dept Orthopaed Surg, Tissue Engn Grp,Fac Med, Natl Orthopaed Ctr Excellence Res & Learning, Kuala Lumpur 50603, Malaysia
关键词
iPSC; iPC; pluripotent; reprogramming cancer cells; stem cells; PLURIPOTENT STEM-CELLS; FGF PATHWAYS COOPERATE; HUMAN FIBROBLASTS; MOUSE; DIFFERENTIATION; EXPRESSION; ACTIVIN; LINES; HETEROGENEITY; GENERATION;
D O I
10.1517/14712598.2016.1174211
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Cancer is a disease with genetic and epigenetic origins, and the possible effects of reprogramming cancer cells using the defined sets of transcription factors remain largely uninvestigated. In the handful of publications available so far, findings have shown that reprogramming cancer cells changed the characteristics of the cells to differ from the parental cancer cells. These findings indicated the possibility of utilizing reprogramming technology to create a disease model in the laboratory to be used in studying the molecular pathogenesis or for drug screening of a particular cancer model.Areas covered: Despite numerous methods employed in generating induced pluripotent stem cells (iPSCs) from cancer cells only a few studies have successfully reprogrammed malignant human cells. In this review we will provide an overview on i) methods to reprogram cancer cells, ii) characterization of the reprogrammed cancer cells, and iii) the differential effects of reprogramming on malignancy, epigenetics and response of the cancer cells to chemotherapeutic agents.Expert opinion: Continued technical progress in cancer cell reprogramming technology will be instrumental for more refined in vitro disease models and ultimately for the development of directed and personalized therapy for cancer patients in the future.
引用
收藏
页码:941 / 951
页数:11
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