Recent advances in searching c-Myc transcriptional cofactors during tumorigenesis

被引:41
作者
Caforio, Matteo [1 ]
Sorino, Cristina [2 ]
Iacovelli, Stefano [1 ]
Fanciulli, Maurizio [2 ]
Locatelli, Franco [1 ,3 ]
Folgiero, Valentina [1 ]
机构
[1] Bambino Gesu Pediat Hosp, Dept Pediat Hematol Oncol & Cell & Gene Therapy, I-00146 Rome, Italy
[2] Regina Elena Inst Canc Res, SAFU, Dept Res Adv Diagnost & Technol Innovat, Translat Res Area, I-00144 Rome, Italy
[3] Univ Pavia, Dept Pediat Sci, I-27100 Pavia, Italy
来源
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH | 2018年 / 37卷
关键词
c-Myc; Transcription cofactors; Tumorigenesis; YES-ASSOCIATED PROTEIN; DNA-DAMAGE RESPONSE; CELL-PROLIFERATION; HIPPO PATHWAY; HEPATOCELLULAR-CARCINOMA; BIOINFORMATIC ANALYSIS; DEPENDENT REPRESSION; SIGNALING PATHWAY; SWI/SNF COMPLEX; POOR-PROGNOSIS;
D O I
10.1186/s13046-018-0912-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The mechanism by which c-Myc exerts its oncogenic functions is not completely clear and different hypotheses are still under investigation. The knowledge of the capacity of c-Myc to bind exclusively E-box sequences determined the discrepancy between, on the one hand, genomic studies showing the binding of c-Myc to all active promoters and, on the other hand, the evidence that only 60% or less of the binding sites have E-box sequences. Main body: In this review, we provide support to the hypothesis that the cooperation of c-Myc with transcriptional cofactors mediates c-Myc-induced cellular functions. We produce evidence that recently identified cofactors are involved in c-Myc control of survival mechanisms of cancer cells. Conclusion: The identification of new c-Myc cofactors could favor the development of therapeutic strategies able to compensate the difficulty of targeting c-Myc.
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页数:9
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