Zhou Ying, Xu Fei, Tao Feng, Feng Dingqing, Ling Bin, Qian Lili, Yang Xia, Wang Qingyuan, Wang Huiyan, Zhao Weidong, Cheng Yong, Shan Ge, Kalvakolanu Dhan V, Xiao Weihua
1 Department of Obstetrics and Gynecology, Anhui Provincial Hospital Affiliated to Anhui Medical University , Hefei, China .
2 Department of Oncological Radiotherapy, Anhui Provincial Hospital Affiliated to Anhui Medical University , Hefei, China .
J Interferon Cytokine Res. 2016 Aug;36(8):506-15. doi: 10.1089/jir.2015.0125. Epub 2016 May 4.
High telomerase activity promotes tumor growth by stabilizing damaged chromosomes and their mitotic replication. Overactivation of telomerase activity has been reported in cervical cancer, a malignancy caused by high-risk human papillomaviruses (HR-HPVs). The HR-HPV E6 can activate hTERT promoter by interacting with E6AP or other binding proteins and by stabilizing the interaction between hTERT and E6AP. GRIM-19 is a novel tumor suppressor that affects multiple targets in a cell to regulate growth. We have previously reported the interaction of GRIM-19 with 18E6 and E6AP to disrupt the E6/E6AP complex and increase the autoubiquitination of E6AP. In this study, we characterized the interaction of GRIM-19 with 16E6 (an oncoprotein produced by HPV16) and identified the binding sites that mediate this interaction. We also found that GRIM-19 expression in cervical cancer cells could inhibit telomerase activity by inhibiting the transactivation of the hTERT promoter by E6, thereby promoting cervical cancer cell senescence. Moreover, we identified a negative correlation between GRIM-19 and hTERT expression in cervical cancer tissues. Suppression of GRIM-19 and induction of hTERT levels were associated with lymph node metastasis, advanced clinical stage, and poor prognosis. This study identified another important novel antitumor molecular link associated with GRIM-19 in the tumorigenesis.
端粒酶活性升高通过稳定受损染色体及其有丝分裂复制来促进肿瘤生长。在宫颈癌(一种由高危型人乳头瘤病毒(HR-HPVs)引起的恶性肿瘤)中,已报道端粒酶活性过度激活。HR-HPV E6可通过与E6相关蛋白(E6AP)或其他结合蛋白相互作用,并通过稳定人端粒酶逆转录酶(hTERT)与E6AP之间的相互作用来激活hTERT启动子。GRIM-19是一种新型肿瘤抑制因子,可影响细胞中的多个靶点以调节生长。我们之前报道过GRIM-19与18E6和E6AP相互作用,破坏E6/E6AP复合物并增加E6AP的自身泛素化。在本研究中,我们对GRIM-19与16E6(一种由HPV16产生的癌蛋白)的相互作用进行了表征,并确定了介导这种相互作用的结合位点。我们还发现,GRIM-19在宫颈癌细胞中的表达可通过抑制E6对hTERT启动子的反式激活来抑制端粒酶活性,从而促进宫颈癌细胞衰老。此外,我们在宫颈癌组织中发现GRIM-19与hTERT表达呈负相关。GRIM-19的抑制和hTERT水平的诱导与淋巴结转移、临床晚期和预后不良有关。本研究确定了GRIM-19在肿瘤发生过程中另一个重要的新型抗肿瘤分子联系。