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本文引用的文献

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Detection in fecal DNA of colon cancer-specific methylation of the nonexpressed vimentin gene.在粪便DNA中检测未表达的波形蛋白基因的结肠癌特异性甲基化。
J Natl Cancer Inst. 2005 Aug 3;97(15):1124-32. doi: 10.1093/jnci/dji204.
2
Fecal DNA biomarkers for the detection of colorectal neoplasia: attractive, but is it feasible?用于检测结直肠肿瘤的粪便DNA生物标志物:有吸引力,但可行吗?
J Natl Cancer Inst. 2005 Aug 3;97(15):1107-9. doi: 10.1093/jnci/dji244.
3
Fecal DNA versus fecal occult blood for colorectal-cancer screening in an average-risk population.平均风险人群中粪便DNA与粪便潜血用于结直肠癌筛查的比较
N Engl J Med. 2004 Dec 23;351(26):2704-14. doi: 10.1056/NEJMoa033403.
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Methylation changes in faecal DNA: a marker for colorectal cancer screening?粪便DNA中的甲基化变化:结直肠癌筛查的标志物?
Lancet. 2004 Apr 17;363(9417):1283-5. doi: 10.1016/S0140-6736(04)16002-9.
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Fecal multiple molecular tests to detect colorectal cancer in stool.
Clin Gastroenterol Hepatol. 2003 Sep;1(5):377-83. doi: 10.1053/s1542-3565(03)00186-1.
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High frequency of mutations of the PIK3CA gene in human cancers.PIK3CA基因在人类癌症中突变频率较高。
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Preferential isolation of fragmented DNA enhances the detection of circulating mutated k-ras DNA.
Clin Chem. 2004 Jan;50(1):211-3. doi: 10.1373/clinchem.2003.026914.
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Fecal occult blood screening--trial evidence, practice and beyond.
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Sensitivity and specificity of a stool DNA multitarget assay panel for the detection of advanced colorectal neoplasia.用于检测晚期结直肠肿瘤的粪便DNA多靶点检测试剂盒的敏感性和特异性
Clin Colorectal Cancer. 2003 May;3(1):47-53. doi: 10.3816/CCC.2003.n.011.
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Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status.肿瘤发生:RAF/RAS癌基因与错配修复状态。
Nature. 2002 Aug 29;418(6901):934. doi: 10.1038/418934a.

在多阶段结直肠癌筛查中,检测粪便潜血检测卡粪便样本中的K-ras突变。

Detecting K-ras mutations in stool from fecal occult blood test cards in multiphasic screening for colorectal cancer.

作者信息

Rennert Gad, Kislitsin Dimitry, Brenner Dean E, Rennert Hedy S, Lev Zeev

机构信息

Department of Community Medicine and Epidemiology, CHS National Cancer Control Center, Carmel Medical Center, Technion, Haifa 34362, Israel.

出版信息

Cancer Lett. 2007 Aug 18;253(2):258-64. doi: 10.1016/j.canlet.2007.01.023. Epub 2007 Mar 8.

DOI:10.1016/j.canlet.2007.01.023
PMID:17349741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2712669/
Abstract

Fecal occult blood testing (FOBT) is proven an efficient way of reducing mortality from colorectal cancer but has a relatively low positive predictive value (PPV). This study evaluated the ability to detect K-ras mutations in stool DNA from FOBT cards and to improve the PPV of the screening process. Two hundred and five consecutive positive FOBT cards and an arbitrary sample of 38 negative cards from a population-based screening program were included. K-ras mutations in FOBT card stool were sought using allele-specific hybridization. DNA was successfully amplified from 87.2% of cards. In 130 cases with positive FOBT and amplifiable DNA 23 malignancies and 25 adenomas were detected. In 34.8% of the malignancies, a mutation in K-ras was detected. The PPV for malignancies increased from 17.7% (all positive cards) to 60.0% if cards with four or more fields were positive and K-ras was positive (RR=2.66, 95% CI: 1.2-6.1). Testing for K-ras mutations in DNA extracted from stool from positive FOBT cards is feasible. Sequential detection of cancer-associated genetic markers from FOBT-based stool samples may potentially help separate true from false positives in a FOBT-based screening process.

摘要

粪便潜血检测(FOBT)已被证明是降低结直肠癌死亡率的有效方法,但阳性预测值(PPV)相对较低。本研究评估了从FOBT卡检测粪便DNA中K-ras突变的能力以及提高筛查过程PPV的能力。研究纳入了基于人群筛查项目中连续的205张阳性FOBT卡以及38张阴性卡的任意样本。使用等位基因特异性杂交法检测FOBT卡粪便中的K-ras突变。87.2%的卡片成功扩增出DNA。在130例FOBT阳性且DNA可扩增的病例中,检测到23例恶性肿瘤和25例腺瘤。在34.8%的恶性肿瘤中检测到K-ras突变。如果四张或更多视野的卡片呈阳性且K-ras呈阳性,恶性肿瘤的PPV从17.7%(所有阳性卡片)增至60.0%(RR=2.66,95%CI:1.2 - 6.1)。检测FOBT阳性卡粪便中提取的DNA的K-ras突变是可行的。从基于FOBT的粪便样本中顺序检测癌症相关遗传标志物可能有助于在基于FOBT的筛查过程中区分真阳性和假阳性。