Di Jiehui, Tang Juanjuan, Qian Heya, Franklin Derek A, Deisenroth Chad, Itahana Yoko, Zheng Junnian, Zhang Yanping
Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, P.R. China.
Department of Radiation Oncology and Lineberger Comprehensive Cancer Center, School of Medicine, the University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Oncotarget. 2017 May 23;8(39):64657-64669. doi: 10.18632/oncotarget.18112. eCollection 2017 Sep 12.
The tumor suppressor p53 plays a pivotal role in numerous cellular responses as it regulates cell proliferation, metabolism, cellular growth, and autophagy. In order to identify novel p53 target genes, we utilized an unbiased microarray approach and identified as a robust candidate, which belongs to the Ras-related GTP-binding protein superfamily and exhibits increased expression in various human cancers. We demonstrated that p53 increases the intracellular IP3 and Ca levels and decreases the LC3 protein levels through its target gene Rap2B, suggesting that p53 can inhibit the autophagic response triggered by starvation via upregulation of the Rap2B-PLCε-IP3-Ca pathway. As a confirmed target gene of p53, we believe that further investigating potential functions of Rap2B in autophagy and tumorigenesis will provide a novel strategy for cancer therapy.
肿瘤抑制因子p53在众多细胞反应中起关键作用,因为它调节细胞增殖、代谢、细胞生长和自噬。为了鉴定新的p53靶基因,我们采用了一种无偏向性的微阵列方法,并鉴定出一个强有力的候选基因,它属于Ras相关GTP结合蛋白超家族,且在多种人类癌症中表达增加。我们证明,p53通过其靶基因Rap2B增加细胞内IP3和Ca水平,并降低LC3蛋白水平,这表明p53可通过上调Rap2B-PLCε-IP3-Ca途径抑制饥饿触发的自噬反应。作为p53的一个已确认的靶基因,我们相信进一步研究Rap2B在自噬和肿瘤发生中的潜在功能将为癌症治疗提供一种新策略。