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Targeting of epigenetic regulators in neuroblastoma
Luz Jubierre,Carlos Jiménez,Eric Rovira,Aroa Soriano,Constantino Sábado,Luis Gros,Anna Llort,Raquel Hladun,Josep Roma,Josep Sánchez de Toledo,Soledad Gallego,Miguel F. Segura 생화학분자생물학회 2018 Experimental and molecular medicine Vol.50 No.-
Approximately 15,000 new cases of pediatric cancer are diagnosed yearly in Europe, with 8–10% corresponding to neuroblastoma, a rare disease with an incidence of 8–9 cases per million children <15 years of age. Although the survival rate for low-risk and intermediate-risk patients is excellent, half of children with high-risk, refractory, or relapsed tumors will be cured, and two-thirds of the other half will suffer major side effects and life-long disabilities. Epigenetic therapies aimed at reversing the oncogenic alterations in chromatin structure and function are an emerging alternative against aggressive tumors that are or will become resistant to conventional treatments. This approach proposes targeting epigenetic regulators, which are proteins that are involved in the creation, detection, and interpretation of epigenetic signals, such as methylation or histone post-translational modifications. In this review, we focused on the most promising epigenetic regulators for targeting and current drugs that have already reached clinical trials.