Abstract 2089: Epigenetic regulation of sprouty2 in colorectal cancer

Alexei J. Stuckel, S. Khare
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引用次数: 0

Abstract

Background: The specific role of Sprouty-2 in colorectal cancer (CRC) as either a tumor suppressor or an oncogene is unclear. This is further obscured by the fact that no known driver mutations of Sprouty-2 have been reported. Therefore, for the first time, alterations of DNA 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) were investigated to better understand the regulation of Sprouty-2 in CRC. Methods: Sprouty-2 transcript expression was evaluated in CRC patient samples and Sprouty-2 protein expression was evaluated in CRC cells. The DNA methylation status spanning Sprouty-2 gene was evaluated using combined bisulfite restriction analysis (COBRA). The 5hmC status in the Sprouty-2 gene body and promoter was analyzed using previously performed nano-hmC-seal data from colon cancers and adjacent normal colonic mucosa. Publicly available RNA-seq and methylation data from The Cancer Genome Atlas (TCGA) were extracted from tumors from CRC patients. Results: Variable Sprouty-2 mRNA expression was observed among CRC patient tumors compared to adjacent normal appearing colonocytes. For the first time, differential methylation between adjacent normal colon and CRC samples was identified in 2 CTCF binding sites and in the promoter near the Transcriptional Start Site (TSS) of Sprouty-2, where the 5mC status in 1 of the CTCF binding sites correlated with transcript abundance. In CRC, this is the first study to reveal increases of 5hmC deposition in the gene body and promoter region of Sprouty-2 compared to normal colon. In metastatic CRC, an inverse correlation of increased Sprouty-2 promoter 5mC and decreased mRNA expression was found in patients registered in TCGA. Conclusions: In terms of tumor growth, epigenetic aberrations including Sprouty-2 promoter hypomethylation and increased 5hmC may play a prominent role in positive regulation of Sprouty-2 in CRC. In metastatic stages of CRC, increases in Sprouty-2 promoter 5mC may downregulate Sprouty-2 expression, which may ultimately label Sprouty-2 as a tumor suppressor in CRC. Citation Format: Alexei Stuckel, Sharad Khare. Epigenetic regulation of sprouty2 in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2089.
2089: sprouty2在结直肠癌中的表观遗传调控
背景:Sprouty-2在结直肠癌(CRC)中作为肿瘤抑制因子或致癌基因的具体作用尚不清楚。Sprouty-2没有已知的驱动突变的报道,这一事实进一步模糊了这一点。因此,我们首次研究了DNA 5-甲基胞嘧啶(5mC)和5-羟甲基胞嘧啶(5hmC)的改变,以更好地了解Sprouty-2在结直肠癌中的调控作用。方法:检测CRC患者样本中Sprouty-2转录物的表达,检测CRC细胞中Sprouty-2蛋白的表达。采用复合亚硫酸氢盐限制性分析(COBRA)对Sprouty-2基因的DNA甲基化状态进行了评价。5hmC在Sprouty-2基因体和启动子中的状态使用先前从结肠癌和邻近正常结肠粘膜中获得的纳米hmc -seal数据进行了分析。从结直肠癌患者的肿瘤中提取癌症基因组图谱(TCGA)中公开可用的RNA-seq和甲基化数据。结果:与邻近正常结肠细胞相比,结直肠癌患者肿瘤中Sprouty-2 mRNA表达变化。首次在相邻正常结肠和结直肠癌样本的2个CTCF结合位点和Sprouty-2转录起始位点(Transcriptional Start Site, TSS)附近的启动子中发现了差异甲基化,其中1个CTCF结合位点的5mC状态与转录物丰度相关。在结直肠癌中,本研究首次发现与正常结肠相比,Sprouty-2基因体和启动子区域的5hmC沉积增加。在转移性结直肠癌中,在TCGA登记的患者中发现Sprouty-2启动子5mC升高与mRNA表达降低呈负相关。结论:在肿瘤生长方面,Sprouty-2启动子低甲基化和5hmC升高等表观遗传畸变可能在CRC中Sprouty-2的正调控中发挥突出作用。在CRC的转移阶段,Sprouty-2启动子5mC的增加可能下调Sprouty-2的表达,这可能最终将Sprouty-2标记为CRC的肿瘤抑制因子。引文格式:Alexei Stuckel, Sharad Khare。结直肠癌中sprouty2的表观遗传调控[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第2089期。
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