Common Themes of Dedifferentiation in Somatic Cell Reprogramming and Cancer

被引:59
作者
Daley, G. Q. [1 ]
机构
[1] Childrens Hosp Boston, Div Pediat Hematol & Oncol, Boston, MA 02115 USA
来源
CONTROL AND REGULATION OF STEM CELLS | 2008年 / 73卷
关键词
D O I
10.1101/sqb.2008.73.041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With its hallmarks of unregulated cell proliferation and compromised differentiation. cancer represents a derangement of normal tissue homeostasis. A common set of pathways are activated in the transformed state, through either mutation or altered epigenetic regulation, and both heritable effects sustain the tumor. Classical views of cancer have invoked tissue dedifferentiation in the oncogenic process, whereas modern views embodied in the cancer stem cell hypothesis hold that cancer emerges from primitive tissue stem cells or specific progenitor populations that through mutations assume the self-renewal properties of stem cells. Recently, somatic tissues have been reprogrammed to it pluripotent state resembling embryonic stem (ES) cells by ectopic expression of a cocktail of transcription factors. The factors that drive reprogramming are oncogenes or have been linked to cellular transformation, suggesting that tumorigenesis and somatic cell reprogramming might indeed share common mechanisms of dedifferentiation.
引用
收藏
页码:171 / 174
页数:4
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共 43 条
[1]  
Abelev G I, 1971, Adv Cancer Res, V14, P295, DOI 10.1016/S0065-230X(08)60523-0
[2]   Control of differentiation in progression of epithelial tumors [J].
Abelev, Garry I. ;
Lazarevich, Natalia L. .
ADVANCES IN CANCER RESEARCH, VOL 95, 2006, 95 :61-113
[3]   let-7 microRNA functions as a potential growth suppressor in human colon cancer cells [J].
Akao, Yukihiro ;
Nakagawa, Yoshihito ;
Naoe, Tomoki .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (05) :903-906
[4]   HETEROCHRONIC MUTANTS OF THE NEMATODE CAENORHABDITIS-ELEGANS [J].
AMBROS, V ;
HORVITZ, HR .
SCIENCE, 1984, 226 (4673) :409-416
[5]   Generation of pluripotent stem cells from adult mouse liver and stomach cells [J].
Aoi, Takashi ;
Yae, Kojiro ;
Nakagawa, Masato ;
Ichisaka, Tomoko ;
Okita, Keisuke ;
Takahashi, Kazutoshi ;
Chiba, Tsutomu ;
Yamanaka, Shinya .
SCIENCE, 2008, 321 (5889) :699-702
[6]   Regulation by let-7 and lin-4 miRNAs results in target mRNA degradation [J].
Bagga, S ;
Bracht, J ;
Hunter, S ;
Massirer, K ;
Holtz, J ;
Eachus, R ;
Pasquinelli, AE .
CELL, 2005, 122 (04) :553-563
[7]   Localization of the developmental timing regulator Lin28 to mRNP complexes, P-bodies and stress granules [J].
Balzer, Erica ;
Moss, Eric G. .
RNA BIOLOGY, 2007, 4 (01) :16-25
[8]   Transitions between epithelial and mesenchymal states in development and disease [J].
Baum, Buzz ;
Settleman, Jeffrey ;
Quinlan, Margaret P. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (03) :294-308
[9]   An embryonic stem cell-like gene expression signature in poorly differentiated aggressive human tumors [J].
Ben-Porath, Ittai ;
Thomson, Matthew W. ;
Carey, Vincent J. ;
Ge, Ruping ;
Bell, George W. ;
Regev, Aviv ;
Weinberg, Robert A. .
NATURE GENETICS, 2008, 40 (05) :499-507
[10]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353