结直肠癌
医学
DNA甲基化
内科学
生物标志物
癌症
甲基化
胃肠病学
CpG站点
肿瘤科
生物
基因
遗传学
基因表达
作者
Yuguang Shen,Dongyang Wang,Tianli Yuan,Hongsheng Fang,Chen Zhu,Juan Qin,Xiaojing Xu,Cheng Zhang,Jiahua Liu,Yuanruohan Zhang,Zhoujin Wen,Jian Tang,Zheng Wang
标识
DOI:10.1186/s13148-023-01443-7
摘要
Early detection and prevention of precancerous lesions can significantly reduce the morbidity and mortality of colorectal cancer (CRC). Here, we developed new candidate CpG site biomarkers for CRC and evaluated the diagnostic value of their expression in blood and stool samples of CRC and precancerous lesions.We analyzed 76 pairs of CRC and adjacent normal tissue samples, 348 stool samples, and 136 blood samples. Candidate biomarkers for CRC were screened using a bioinformatics database and identified using a quantitative methylation-specific PCR method. The methylation levels of the candidate biomarkers were validated using blood and stool samples. The divided stool samples were used to construct and validate a combined diagnostic model and to analyze the independent or combined diagnostic value of candidate biomarkers in stool samples of CRC and precancerous lesions.Two candidate CpG site biomarkers for CRC, cg13096260 and cg12993163, were identified. Although both biomarkers demonstrated diagnostic performance to a certain extent when using blood samples, they showed better diagnostic value for different stages of CRC and AA with stool samples.cg13096260 and cg12993163 detection in stool samples could be a promising approach for screening and early diagnosis of CRC and precancerous lesions.
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