Musa Julian, Aynaud Marie-Ming, Mirabeau Olivier, Delattre Olivier, Grünewald Thomas Gp
Max-Eder Research Group for Pediatric Sarcoma Biology, Institute for Pathology of the LMU Munich, Munich, Germany.
INSERM Unit 830 'Genetics and Biology of Cancers', Institut Curie Research Center, Paris, France.
Cell Death Dis. 2017 Jun 22;8(6):e2895. doi: 10.1038/cddis.2017.244.
Limitless cell proliferation, evasion from apoptosis, dedifferentiation, metastatic spread and therapy resistance: all these properties of a cancer cell contribute to its malignant phenotype and affect patient outcome. MYBL2 (alias B-Myb) is a transcription factor of the MYB transcription factor family and a physiological regulator of cell cycle progression, cell survival and cell differentiation. When deregulated in cancer cells, MYBL2 mediates the deregulation of these properties. In fact, MYBL2 is overexpressed and associated with poor patient outcome in numerous cancer entities. MYBL2 and players of its downstream transcriptional network can be used as prognostic and/or predictive biomarkers as well as potential therapeutic targets to offer less toxic and more specific anti-cancer therapies in future. In this review, we summarize current knowledge on the physiological roles of MYBL2 and highlight the impact of its deregulation on cancer initiation and progression.
无限的细胞增殖、逃避凋亡、去分化、转移扩散和治疗抗性:癌细胞的所有这些特性都促成了其恶性表型,并影响患者的预后。MYBL2(别名B-Myb)是MYB转录因子家族的转录因子,也是细胞周期进程、细胞存活和细胞分化的生理调节因子。当在癌细胞中失调时,MYBL2介导这些特性的失调。事实上,在众多癌症实体中,MYBL2表达上调且与患者预后不良相关。MYBL2及其下游转录网络的相关因子可作为预后和/或预测生物标志物以及潜在的治疗靶点,以便在未来提供毒性更小、更具特异性的抗癌疗法。在本综述中,我们总结了目前关于MYBL2生理作用的知识,并强调了其失调对癌症发生和进展的影响。