甲基化
DNA甲基化
寡核苷酸
照明菌甲基化试验
甲基化DNA免疫沉淀
分子生物学
去甲基化
DNA
亚硫酸氢盐测序
生物
基因
化学
生物化学
基因表达
作者
Jing Su,Shasha Song,Yanzhi Dou,Xiaolong Jia,Shiping Song,Xianting Ding
标识
DOI:10.1016/j.bios.2023.115587
摘要
Methylation of the promoter region of cancer related genes plays a crucial role in the occurrence and development of cancer, and the degree of methylation has great potential for the early cancer diagnosis. At present, the technology used to quantify DNA methylation is mainly based on the DNA sequencing which are time-consuming and high-cost in the relating application. We have developed an ultrasensitive method of methylation specific enzyme-linked oligonucleotide assays (MS-ELONA) to detect and quantify the level of DNA methylation. We could detect as little as 2 pg of methylated DNA in the 100000-fold excess of unmethylated genes, and discriminate prostate cancer from benign prostatic hyperplasia (BPH) and control with serum samples. We also demonstrate the reversibility of DNA methylation modification by treatment with demethylation drugs. With 16-channel electrochemical work station, our research reveals a simple and inexpensive method to quantify the methylation level of specially appointed genes, and have the potential to be applied in the clinical research.
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