Stacking the DEK From chromatin topology to cancer stem cells

被引:61
作者
Vinnedge, Lisa M. Privette [1 ]
Kappes, Ferdinand [2 ]
Nassar, Nicolas [1 ]
Wells, Susanne I. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Canc & Blood Dis Inst, Cincinnati, OH USA
[2] Rhein Westfal TH Aachen, Sch Med, Inst Biochem & Mol Biol, Aachen, Germany
基金
美国国家卫生研究院;
关键词
chromatin organization; stem cells; cancer stem cells; DEK; heterochromatin; ACUTE MYELOID-LEUKEMIA; SOLUTION NMR STRUCTURE; TUMOR-SUPPRESSOR P53; N-TERMINAL DOMAIN; SELF-RENEWAL; PROTEIN DEK; INITIATING CELLS; IN-VITRO; FUNCTIONAL ASSAYS; SIDE POPULATION;
D O I
10.4161/cc.23121
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stem cells are essential for development and tissue maintenance and display molecular markers and functions distinct from those of differentiated cell types in a given tissue. Malignant cells that exhibit stem cell-like activities have been detected in many types of cancers and have been implicated in cancer recurrence and drug resistance. Normal stem cells and cancer stem cells have striking commonalities, including shared cell surface markers and signal transduction pathways responsible for regulating quiescence vs. proliferation, self-renewal, pluripotency and differentiation. As the search continues for markers that distinguish between stem cells, progenitor cells and cancer stem cells, growing evidence suggests that a unique chromatin-associated protein called DEK may confer stem cell-like qualities. Here, we briefly describe current knowledge regarding stem and progenitor cells. We then focus on new findings that implicate DEK as a regulator of stem and progenitor cell qualities, potentially through its unusual functions in the regulation of local or global chromatin organization.
引用
收藏
页码:51 / 66
页数:16
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