摘要5064:Sirt6是人类尿路上皮癌中一种新的肿瘤抑制因子,可被甲基化酶激活

Dongjun Fu, N. Yokoyama, Mattew Tippin, X. Zi
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引用次数: 0

摘要

Sirtuin 6 (SIRT6)在长寿、代谢、dna修复和炎症反应中发挥重要作用。在人类尿路上皮癌中,SIRT6的高水平表达预示着患者更好的生存。我们发现SIRT6在人肌肉侵袭性膀胱癌细胞系J82中过表达可降低细胞迁移和侵袭,但不降低体外细胞生长。卡瓦是一种传统的精神药物饮料,由胡椒根状茎制成。以前的流行病学研究表明,在南太平洋岛屿国家,癌症发病率与卡瓦的消费量呈反比关系。我们已经证明,卡瓦植物中的一种主要的卡瓦内酯甲藻素(Methysticin)可以抑制膀胱癌细胞株的生长、迁移和侵袭。然而,在SIRT6低表达、酶促突变SIRT6表达或SIRT6敲除的细胞中,Methysticin的这些抗癌活性减弱,这表明Methysticin的抗癌活性至少部分依赖于SIRT6的表达。分子模型表明,Methysticin停靠在SIRT6乙酰化肽底物结合位点附近的环旁边。细胞热移实验(CETSA,一种体内实验)表明,甲基甲氧嘧啶显著降低了热诱导的SIRT6蛋白降解。Methysticin处理J82细胞也导致H3K18乙酰化的剂量依赖性降低。综上所述,这些结果表明,甲藻素是一种新的SIRT6激活剂,具有抗膀胱活性。进一步的研究表明,甲氧麻黄素通过增加TBK1的蛋白表达以及TBK1和STING的磷酸化,激活TBK1/IRF3/STING通路,提示甲氧麻黄素可能具有增强抗肿瘤免疫的作用。因此,我们的结果支持进一步研究甲基化对膀胱癌预防的作用。注:本摘要未在会议上提交。引用格式:付东军,Noriko N. Yokoyama, matthew Tippin, Xiaolin Zi。Sirt6是人类尿路上皮癌中一种新型肿瘤抑制因子,可被甲基化酶激活[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):5064。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 5064: Sirt6 is a novel tumor suppressor in human urothelial cancer and activated by methysticin
Sirtuin 6 (SIRT6) plays an important role in longevity, metabolism, DNA-repair, and inflammatory response. In human urothelial cancer, a high level of SIRT6 expression predicts a better survival for patients. We found that overexpression of SIRT6 in human muscle-invasive bladder cancer cell line J82 reduced cell migration and invasion, but didn’t reduce the in vitro cell growth. Kava is a traditional psychotropic beverage made from the rhizomes of Piper methysticum G. Forst. Previous epidemiological studies have shown an inverse relationship between cancer incidence and kava consumption in South Pacific Island Nations. We have shown that Methysticin, a major kavalactone in the Kava plant, inhibits the growth, migration and invasion of bladder cancer lines. However, these anti-cancer activities of Methysticin are attenuated in cells with low expression of SIRT6, expression of enzymatically mutant SIRT6 or SIRT6 knockout, which suggested that the anti-cancer activities of Methysticin are at least in part dependent on SIRT6 expression. Molecular modelling indicates that Methysticin docks into the site next to a loop near the acetylated peptide substrate binding site of SIRT6. The Cellular Thermal Shift Assay (CETSA, an in vivo assay) demonstrated that Methysticin significantly decreased heat-induced protein degradation of SIRT6. Treatment of J82 cells with Methysticin also resulted in a dose-dependent reduction of H3K18 acetylation. Taken together, these results suggest that Methysticin acts a novel SIRT6 activator for its anti-bladder activity. Further studies have demonstrated that Methysticin activates the TBK1/IRF3/STING pathway by increasing the protein expression of TBK1 and the phosphorylation of TBK1 and STING, which suggest that Methysticin may be able to enhance anti-tumor immunity. Therefore, our results support further investigation of Methylation for bladder cancer prevention. Note: This abstract was not presented at the meeting. Citation Format: DongJun Fu, Noriko N. Yokoyama, Mattew Tippin, Xiaolin Zi. Sirt6 is a novel tumor suppressor in human urothelial cancer and activated by methysticin [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 5064.
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