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巴西结直肠癌患者微卫星不稳定性评估。

Assessment of microsatellite instability in colorectal cancer patients from Brazil.

作者信息

Leite Sinara M O, Gomes Karina B, Pardini Victor C, Ferreira Alessandro C S, Oliveira Vanessa C, Cruz Geraldo M G

机构信息

Department of Coloproctology, Santa Casa de Belo Horizonte, MG, Brazil.

出版信息

Mol Biol Rep. 2010 Jan;37(1):375-80. doi: 10.1007/s11033-009-9807-9.

Abstract

UNLABELLED

The replication error status analysis of DNA, through microsatellite instability detection, has become an indispensable tool for hereditary non-polyposis colorectal cancer screening. This study investigated the microsatellite instability in Brazilian individuals presenting colorectal cancer. In this study, 66 patients were clinically analyzed according to Amsterdam II and Bethesda guidelines. Normal and tumour tissues were collected and analyzed for MSI degree according to molecular markers BAT25, BAT26, BAT40, APC-D5S346, D2S123, and D17S250. Eight patients (12.1%) fulfilled the Amsterdam II guidelines, and 15 (22.7%) met the Bethesda guidelines. BAT25 was the most sensitive marker (86.7%), while BAT26 was the least sensitive (66.7%). The specificity of both markers was 100%, but all of the markers must be used since the contribution of each marker to the sensitivity and specificity of the test is complementary. Proximal tumours were significantly predominant among RER+ patients.

CONCLUSIONS

Patients with a family history of colorectal cancer with the tumour in the proximal colon must be screened to replication error status as early as possible in order to avoid the progression of the disease.

摘要

未标注

通过微卫星不稳定性检测对DNA的复制错误状态进行分析,已成为遗传性非息肉病性结直肠癌筛查不可或缺的工具。本研究调查了患有结直肠癌的巴西个体的微卫星不稳定性。在本研究中,根据阿姆斯特丹II和贝塞斯达指南对66例患者进行了临床分析。收集正常组织和肿瘤组织,并根据分子标记物BAT25、BAT26、BAT40、APC-D5S346、D2S123和D17S250分析微卫星不稳定性程度。8例患者(12.1%)符合阿姆斯特丹II指南,15例(22.7%)符合贝塞斯达指南。BAT25是最敏感的标记物(86.7%),而BAT26最不敏感(66.7%)。两种标记物的特异性均为100%,但必须使用所有标记物,因为每个标记物对检测的敏感性和特异性的贡献是互补的。RER+患者中近端肿瘤明显占优势。

结论

有结直肠癌家族史且肿瘤位于近端结肠的患者必须尽早进行复制错误状态筛查,以避免疾病进展。

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