核仁
核糖体
生物
核糖体RNA
抄写(语言学)
核糖体蛋白
癌症
癌症研究
基因
转录活性
核糖体生物发生
转录因子
核糖核酸
细胞生物学
遗传学
细胞质
语言学
哲学
作者
Nadine Hein,Katherine M. Hannan,Amee J. George,Elaine Sanij,Ross D. Hannan
标识
DOI:10.1016/j.molmed.2013.07.005
摘要
For over 100 years, pathologists have utilised an increase in size and number of nucleoli, the subnuclear site of ribosome synthesis, as a marker of aggressive tumours. Despite this, the contribution of the nucleolus and ribosomal RNA synthesis to cancer has been largely overlooked. This concept has recently changed with the demonstration that the nucleolus indirectly controls numerous other cellular functions, in particular, the cellular activity of the critical tumour suppressor protein, p53. Moreover, selective inhibition of ribosomal gene transcription in the nucleolus has been shown to be an effective therapeutic strategy to promote cancer-specific activation of p53. This article reviews the largely untapped potential of the nucleolus and ribosomal gene transcription as exciting new targets for cancer therapy.
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