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本文引用的文献

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Incidence of hereditary non-polyposis colorectal cancer in a population-based study of 1137 consecutive cases of colorectal cancer.在一项基于人群的1137例连续结直肠癌病例研究中遗传性非息肉病性结直肠癌的发病率
Br J Surg. 1997 Sep;84(9):1281-5.
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Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.不符合阿姆斯特丹标准的遗传性非息肉病性结直肠癌家族中,错配修复基因突变的频率极低。
Am J Hum Genet. 1997 Aug;61(2):329-35. doi: 10.1086/514847.
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Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review.遗传性非息肉病性结直肠癌(林奇综合征)。最新综述。
Cancer. 1996 Sep 15;78(6):1149-67. doi: 10.1002/(SICI)1097-0142(19960915)78:6<1149::AID-CNCR1>3.0.CO;2-5.
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Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.遗传性非息肉病性结直肠癌患者错配修复基因分析
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Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology.利用微卫星和荧光DNA技术快速检测结直肠肿瘤中的等位基因缺失
Br J Cancer. 1993 Jun;67(6):1262-7. doi: 10.1038/bjc.1993.236.
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Clues to the pathogenesis of familial colorectal cancer.家族性结直肠癌的发病机制线索。
Science. 1993 May 7;260(5109):812-6. doi: 10.1126/science.8484121.
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Genetic mapping of a locus predisposing to human colorectal cancer.一个易患人类结直肠癌位点的基因定位。
Science. 1993 May 7;260(5109):810-2. doi: 10.1126/science.8484120.
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Cancer risk in relatives of patients with common colorectal cancer.常见结直肠癌患者亲属的癌症风险
Ann Intern Med. 1993 May 15;118(10):785-90. doi: 10.7326/0003-4819-118-10-199305150-00005.
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Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history.结直肠癌中的基因组不稳定性:与临床病理变量及家族史的关系。
Cancer Res. 1993 Dec 15;53(24):5849-52.
10
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.DNA错配修复基因同源物hMLH1的突变与遗传性非息肉病性结直肠癌相关。
Nature. 1994 Mar 17;368(6468):258-61. doi: 10.1038/368258a0.

结直肠癌中复制错误的频率及其与家族史的关联。

Frequency of replication errors in colorectal cancer and their association with family history.

作者信息

Brown S R, Finan P J, Cawkwell L, Quirke P, Bishop D T

机构信息

Centre for Digestive Diseases, Leeds General Infirmary, Leeds, UK.

出版信息

Gut. 1998 Oct;43(4):553-7. doi: 10.1136/gut.43.4.553.

DOI:10.1136/gut.43.4.553
PMID:9824585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1727271/
Abstract

BACKGROUND

Replication errors (RERs) characterise tumours of hereditary non-polyposis colorectal cancer (HNPCC). RER status may therefore improve identification of such families previously diagnosed by family history alone.

AIMS

To assess RER and HNPCC frequency within a population of colorectal cancer patients and a regional population of family history defined (Amsterdam criteria) HNPCC families.

METHODS

Family history was assessed by personal interview in a population of 479 patients with colorectal cancer attending one follow up clinic. Seven fluorescently labelled microsatellites were used to investigate RER frequency in colorectal cancers from 89 patients of this population with varying degrees of family history and 20 Amsterdam criteria positive families (four with a known germline mutation, 16 with unknown mutation status) from the regional population.

RESULTS

Only four of the follow up population (0.8%) came from families meeting the Amsterdam criteria with only one showing RERs. The frequency of RERs was similar in the early onset cancer group (less than 50 years of age), those with a family history, and those with no family history of colorectal cancer. From the regional population, RERs were identified in 4/4 families with a mutation but only 8/16 families with unknown mutation status.

CONCLUSIONS

No correlation was seen between RER status and strength of family history except in HNPCC families. Results also indicate that half of the Amsterdam criteria defined families do not exhibit RERs, perhaps suggesting a different mechanism of tumorigenesis.

摘要

背景

复制错误(RERs)是遗传性非息肉病性结直肠癌(HNPCC)肿瘤的特征。因此,RER状态可能有助于更好地识别那些之前仅通过家族史诊断的此类家族。

目的

评估结直肠癌患者群体以及符合家族史定义(阿姆斯特丹标准)的HNPCC家族的区域群体中的RER和HNPCC频率。

方法

通过个人访谈对一家随访诊所的479例结直肠癌患者进行家族史评估。使用七个荧光标记的微卫星来研究该群体中89例具有不同家族史程度的患者的结直肠癌中的RER频率,以及来自区域群体的20个符合阿姆斯特丹标准的阳性家族(4个有已知种系突变,16个突变状态未知)中的RER频率。

结果

随访人群中只有4例(0.8%)来自符合阿姆斯特丹标准的家族,其中只有1例显示RERs。RERs频率在早发性癌症组(年龄小于50岁)、有家族史的患者以及无结直肠癌家族史的患者中相似。在区域群体中,在4个有突变的家族中发现了RERs,但在16个突变状态未知的家族中只有8个发现了RERs。

结论

除了在HNPCC家族中,未发现RER状态与家族史强度之间存在相关性。结果还表明,符合阿姆斯特丹标准的家族中有一半没有表现出RERs,这可能暗示了一种不同的肿瘤发生机制。