Li Qingdi Quentin, Hao Jian-Jiang, Zhang Zheng, Hsu Iawen, Liu Yi, Tao Zhen, Lewi Keidren, Metwalli Adam R, Agarwal Piyush K
Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Poochon Scientific, Frederick, MD 21704, USA.
Int J Oncol. 2016 Jun;48(6):2591-607. doi: 10.3892/ijo.2016.3478. Epub 2016 Apr 7.
The Cancer Genome Atlas (TCGA) project recently identified the importance of mutations in chromatin remodeling genes in human carcinomas. These findings imply that epigenetic modulators might have a therapeutic role in urothelial cancers. To exploit histone deacetylases (HDACs) as targets for cancer therapy, we investigated the HDAC inhibitors (HDACIs) romidepsin, trichostatin A, and vorinostat as potential chemotherapeutic agents for bladder cancer. We demonstrate that the three HDACIs suppressed cell growth and induced cell death in the bladder cancer cell line 5637. To identify potential mechanisms associated with the anti-proliferative and cytotoxic effects of the HDACIs, we used quantitative proteomics to determine the proteins potentially involved in these processes. Our proteome studies identified a total of 6003 unique proteins. Of these, 2472 proteins were upregulated and 2049 proteins were downregulated in response to HDACI exposure compared to the untreated controls (P<0.05). Bioinformatic analysis further revealed that those differentially expressed proteins were involved in multiple biological functions and enzyme-regulated pathways, including cell cycle progression, apoptosis, autophagy, free radical generation and DNA damage repair. HDACIs also altered the acetylation status of histones and non-histone proteins, as well as the levels of chromatin modification proteins, suggesting that HDACIs exert multiple cytotoxic actions in bladder cancer cells by inhibiting HDAC activity or altering the structure of chromatin. We conclude that HDACIs are effective in the inhibition of cell proliferation and the induction of apoptosis in the 5637 bladder cancer cells through multiple cell death-associated pathways. These observations support the notion that HDACIs provide new therapeutic options for bladder cancer treatment and thus warrant further preclinical exploration.
癌症基因组图谱(TCGA)项目最近确定了染色质重塑基因中的突变在人类癌症中的重要性。这些发现表明,表观遗传调节剂可能在尿路上皮癌中具有治疗作用。为了将组蛋白去乙酰化酶(HDAC)作为癌症治疗的靶点,我们研究了HDAC抑制剂(HDACI)罗米地辛、曲古抑菌素A和伏立诺他作为膀胱癌潜在化疗药物的作用。我们证明,这三种HDACI在膀胱癌细胞系5637中抑制细胞生长并诱导细胞死亡。为了确定与HDACI的抗增殖和细胞毒性作用相关的潜在机制,我们使用定量蛋白质组学来确定可能参与这些过程的蛋白质。我们的蛋白质组研究共鉴定出6003种独特的蛋白质。其中,与未处理的对照相比,有2472种蛋白质在HDACI处理后上调,2049种蛋白质下调(P<0.05)。生物信息学分析进一步表明,这些差异表达的蛋白质参与多种生物学功能和酶调节途径,包括细胞周期进程、凋亡、自噬、自由基生成和DNA损伤修复。HDACI还改变了组蛋白和非组蛋白的乙酰化状态,以及染色质修饰蛋白的水平,这表明HDACI通过抑制HDAC活性或改变染色质结构在膀胱癌细胞中发挥多种细胞毒性作用。我们得出结论,HDACI通过多种与细胞死亡相关的途径有效抑制5637膀胱癌细胞的增殖并诱导其凋亡。这些观察结果支持了HDACI为膀胱癌治疗提供新的治疗选择这一观点,因此值得进一步的临床前探索。