中南大学肿瘤研究所,中南大学湘雅二医院,中南大学肿瘤研究所,中南大学肿瘤研究所,中南大学肿瘤研究所,中南大学肿瘤研究所,中南大学肿瘤研究所,中南大学肿瘤研究所,中南大学肿瘤研究所
国家自然科学基金(30871282, 30871365, 30971147, 81172189, 81171930, 81272298), 湖南省自然科学基金(10JJ7003), 霍英东高校青年教师基金(121036), 中央高校基本科研业务费专项资金(2011JQ020), 中南大学米塔尔创新创业项目(11MX27), 中南大学贵重仪器设备开放共享基金及中南大学博士后科学基金资助项目
Caner Research Institute, Central South University;Xiangya Second Hospital, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University,Caner Research Institute, Central South University
This work was supported by grants from The National Natural Science Foundation of China (30871282, 30871365, 30971147, 81172189, 81171930, 81272298), The Hunan Province Natural Science Foundation of China (10JJ7003), The Fok Ying Tong Education Foundation (121036), The Fundamental Research Funds for The Central Universities (2011JQ020), The Mittal Innovative Entrepreneurial Project of Central South University(11MX27), The Open-End Fund for The Valuable and Precision Instruments of Central South University and The Postdoctoral Science Foundation of Central South University
TP53基因(编码p53蛋白)作为一个重要的抑瘤基因,通过调控一系列信号转导通路广泛参与了多种恶性肿瘤的发生发展,一直是肿瘤分子生物学研究领域的热点.最近的研究发现,microRNAs(miRNAs)参与了TP53的信号通路,它们之间存在着复杂的调控网络.一方面,p53通过调控一些miRNAs的转录及转录后成熟,促进细胞周期阻滞、诱导细胞凋亡和衰老,抑制肿瘤发生.另一方面,许多miRNAs,如miR-25、miR-30d、miR-125b和miR-504等可直接调控p53的表达与活性,参与TP53信号通路的调节,还有一些miRNAs则通过调节p53上下游基因,发挥重要的生物学功能.其中,最具有代表性的是miR-34家族,它们受p53直接调控并参与TP53信号通路,通过靶向抑制多个TP53信号通路关键分子的表达,发挥抑瘤作用.此外,它们还可以通过抑制沉默信息调节子,增强p53的活性,反馈调节TP53信号通路.miRNAs与TP53之间调控网络的研究,是对TP53抑瘤机制的重要补充.
The tumor suppressor TP53 gene, which encodes p53 protein, is a hotspot of all time in molecular oncology. p53 suppresses tumor initiation and progression through its regulation of many downstream genes. Recent studies have revealed that microRNAs (miRNAs) interact with the p53 pathway and form a complex regulatory network. On one hand, p53 promotes cell cycle arrest and induces cell apoptosis and senescence to suppress tumorigenesis by regulating the transcription and post-transcriptional maturation of multiple miRNAs. On the other hand, many miRNAs fine-tune the p53 pathway through regulation of TP53 and its upstream regulators or downstream effectors. The miR-34s family, directly transactivated by p53 represents a large number of p53-regulated miRNAs. They exert their tumor suppressing function via targeted inhibition of multiple key molecules in the p53 pathway. Furthermore, miR-34s enhance p53 activity through a feedback loop by inhibiting silent information regulator 1(SIRT 1). Investigation on the interaction between miRNAs and p53 is essential to fully understand the underline mechanisms of p53 tumor suppressing action.
龚朝建,黄宏斌,徐 柯,梁 芳,李小玲,熊 炜,曾朝阳,李桂源. microRNAs与TP53基因调控网络研究进展[J].生物化学与生物物理进展,2012,39(12):1133-1144
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