结直肠癌患者肿瘤组织、粪便和血浆DNA中SFRP2启动子甲基化分析

Yong-Suk Kim, Song-Hak Kim, Myong-Nam Kim, Un-Rim Sim
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引用次数: 2

摘要

非侵入性癌症早期检测是一种有希望为人们提供更高质量医疗服务的方法。结直肠癌患者的血清和粪便中通常含有较高的游离DNA水平,这可能用于癌症检测。由于SFRP2(分泌卷曲相关蛋白2)被认为是一种Wnt抑制剂,其CpGs在几种人类癌症中经常高甲基化,因此我们通过MS-PCR研究了原发性肿瘤和结直肠癌患者血清或粪便样本中SFRP2启动子甲基化异常的频率。我们在117个结直肠癌石蜡包埋组织中的111个(94.9%)中检测到SFRP2甲基化。来自这些病例的68个可用血清样本中有59个(86.8%)携带可检测量的甲基化SFRP2启动子。来自同一病例的68份粪便样本中有61份(89.7%)携带SFRP2基因启动子区甲基化阳性。相比之下,60名健康对照者的血清和粪便样本中未检测到甲基化的SFRP2启动子DNA。68例健康对照中只有2例在结直肠组织中显示SFRP2启动子DNA甲基化。但SFRP2基因启动子甲基化频率高与临床病理特征无关。我们得出结论,SFRP2甲基化分析似乎是血清和/或粪便DNA中的非侵入性肿瘤标志物
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SFRP2 Promoter Methylation Analysis in Tumor Tissue, Stool, and Plasma DNA of Patients with Colorectal Cancer
Noninvasive method for early detection of human cancers is promising way to provide more quality health service to the population. The serum and stool of colorectal cancer patients often harbor increased free DNA levels, which can potentially be used for cancer detection. Because SFRP2 (secreted frizzled related protein 2) is considered a Wnt inhibitor whose CpGs were frequently hypermethylated in several human cancers, we investigated the frequency of aberrant SFRP2 promoter methylation in primary tumors and serum or stool samples of colorectal cancer patients by MS-PCR. We detected methylation of SFRP2 in 111 of 117 (94.9%) paraffin-embedded colorectal cancer tissues. Fifty-nine of the 68 (86.8%) available serum samples from these cases carried detectable amounts of the methylated SFRP2 promoter. Sixty-one of 68 (89.7%) available stool samples from the same cases carried positive methylation in the promoter region of SFRP2 gene. In contrast, no methylated SFRP2 promoter DNA was detected in serum and stool samples from 60 healthy controls. Only 2 cases of 68 healthy controls showed methylated SFRP2 promoter DNA in their colorectal tissue. But high frequency of methylated SFRP2 gene promoter has no correlation with the clinic-pathologic features. We concluded that SFRP2 methylation analysis appeared to be a noninvasive tumor marker in serum and/or stool DNA
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