Molecular mechanisms of ETS transcription factor-mediated tumorigenesis

被引:113
作者
Kar, Adwitiya [1 ]
Gutierrez-Hartmann, Arthur [1 ,2 ,3 ,4 ]
机构
[1] Univ Colorado, Canc Biol Training Program, Aurora, CO 80045 USA
[2] Univ Colorado, Program Mol Biol, Aurora, CO 80045 USA
[3] Univ Colorado, Dept Med, Aurora, CO 80045 USA
[4] Univ Colorado, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
关键词
ETS; ETS activator/repressor switch; ETS fusion; ETS in stroma; ETS in tumorigenesis; ETS overexpression; ETS post-translational modifications; ETS tumorigenic mechanism; ACUTE MYELOID-LEUKEMIA; TERT PROMOTER MUTATIONS; DNA-BINDING SPECIFICITY; BREAST-CANCER; EWINGS-SARCOMA; GROWTH-FACTOR; TERNARY COMPLEX; FUSION PROTEIN; ANDROGEN RECEPTOR; GENE-EXPRESSION;
D O I
10.3109/10409238.2013.838202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The E26 transformation-specific (ETS) family of transcription factors is critical for development, differentiation, proliferation and also has a role in apoptosis and tissue remodeling. Changes in expression of ETS proteins therefore have a significant impact on normal physiology of the cell. Transcriptional consequences of ETS protein deregulation by overexpression, gene fusion, and modulation by RAS/MAPK signaling are linked to alterations in normal cell functions, and lead to unlimited increased proliferation, sustained angiogenesis, invasion and metastasis. Existing data show that ETS proteins control pathways in epithelial cells as well as stromal compartments, and the crosstalk between the two is essential for normal development and cancer. In this review, we have focused on ETS factors with a known contribution in cancer development. Instead of focusing on a prototype, we address cancer associated ETS proteins and have highlighted the diverse mechanisms by which they affect carcinogenesis. Finally, we discuss strategies for ETS factor targeting as a potential means for cancer therapeutics.
引用
收藏
页码:522 / 543
页数:22
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