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本文引用的文献

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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer.MSH6种系突变是遗传性非息肉病性结直肠癌的病因。
Nat Genet. 1997 Nov;17(3):271-2. doi: 10.1038/ng1197-271.
2
Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred.一个非典型遗传性非息肉病性结直肠癌家系中hMSH6/GTBP基因的种系突变。
Cancer Res. 1997 Sep 15;57(18):3920-3.
3
Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers.对25例前瞻性获取的错配修复缺陷(RER+)子宫内膜癌中MLH1和MSH2的突变分析。
Genes Chromosomes Cancer. 1997 Mar;18(3):219-27. doi: 10.1002/(sici)1098-2264(199703)18:3<219::aid-gcc8>3.0.co;2-4.
4
Cancer risk associated with germline DNA mismatch repair gene mutations.与种系DNA错配修复基因突变相关的癌症风险
Hum Mol Genet. 1997 Jan;6(1):105-10. doi: 10.1093/hmg/6.1.105.
5
Pancreatic adenocarcinoma: epidemiology and genetics.胰腺腺癌:流行病学与遗传学
J Med Genet. 1996 Nov;33(11):889-98. doi: 10.1136/jmg.33.11.889.
6
Family history of cancer is a risk factor for squamous cell carcinoma of the head and neck in Brazil: a case-control study.癌症家族史是巴西头颈鳞状细胞癌的一个风险因素:一项病例对照研究。
Int J Cancer. 1995 Dec 11;63(6):769-73. doi: 10.1002/ijc.2910630603.
7
Familial risks of squamous cell carcinoma of the head and neck: retrospective case-control study.头颈部鳞状细胞癌的家族风险:回顾性病例对照研究。
BMJ. 1996 Sep 21;313(7059):716-21. doi: 10.1136/bmj.313.7059.716.
8
A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group.一项基于人群的年轻女性子宫内膜癌与家族风险研究。癌症与类固醇激素研究小组。
Cancer Epidemiol Biomarkers Prev. 1996 Jun;5(6):411-7.
9
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.通过突变分析诊断的遗传性非息肉病性结直肠癌家族中的癌症风险。
Gastroenterology. 1996 Apr;110(4):1020-7. doi: 10.1053/gast.1996.v110.pm8612988.
10
Family history of cancer and risk of lung cancer among lifetime nonsmoking women in the United States.美国终生不吸烟女性的癌症家族史与肺癌风险
Am J Epidemiol. 1996 Mar 15;143(6):535-42. doi: 10.1093/oxfordjournals.aje.a008783.

结直肠癌和子宫内膜癌双原发性癌症的遗传学意义。

Genetic implications of double primary cancers of the colorectum and endometrium.

作者信息

Pal T, Flanders T, Mitchell-Lehman M, MacMillan A, Brunet J S, Narod S A, Foulkes W D

机构信息

The Centre for Research in Women's Health, and The Hospital for Sick Children, University of Toronto, Canada.

出版信息

J Med Genet. 1998 Dec;35(12):978-84. doi: 10.1136/jmg.35.12.978.

DOI:10.1136/jmg.35.12.978
PMID:9863592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1051507/
Abstract

Hereditary non-polyposis colorectal cancer (HNPCC) is an autosomal dominant condition predisposing to cancers of the colorectum and endometrium. Endometrial cancer is the most commonly occurring extracolonic cancer in HNPCC. Estimates of the cumulative incidence of endometrial cancer in women with mutations in the HNPCC genes range from 22-43%. In order to determine how frequently double primary cancers of the colorectum and endometrium are the result of a hereditary factor, we conducted a registry based study in Ontario and Quebec, Canada. We obtained pedigrees on 80 women diagnosed with double primary cancers of the colorectum and endometrium at less than 70 years of age. Family histories of cancer were obtained for all first degree relatives of these women and cancer rates were compared with age standardised provincial incidence rates in order to estimate the relative risks. There was a total of 82 cancers observed in relatives below the age of 55, compared with 31.2 expected, giving a relative risk of 2.6 (95% confidence interval (CI) 2.1-3.3). The relative risk for colorectal cancer below 55 was 16.1 (95% CI 11.6-21.8). This risk decreased with increasing age of onset of cancers in probands. For probands with both colorectal and endometrial cancer diagnosed under the age of 55, the relative risk of colorectal cancer in relatives below the age of 55 was 30.5 (95% CI 18.8-46.6). Similar patterns were observed for endometrial and pancreatic cancer. There were non-significant increases in rates of cancer of the oesophagus, stomach, small intestine, and bladder. There was no increased risk of breast cancer. The risk of lung cancer was decreased, especially in older relatives. Our findings indicate the presence of a significant genetic component of cancer in women with double primary cancers of the colorectum and endometrium.

摘要

遗传性非息肉病性结直肠癌(HNPCC)是一种常染色体显性遗传病,易引发结直肠癌和子宫内膜癌。子宫内膜癌是HNPCC中最常见的结肠外癌症。HNPCC基因突变女性患子宫内膜癌的累积发病率估计在22%至43%之间。为了确定结直肠癌和子宫内膜癌双原发癌由遗传因素导致的频率,我们在加拿大安大略省和魁北克省开展了一项基于登记处的研究。我们获取了80名年龄小于70岁、被诊断患有结直肠癌和子宫内膜癌双原发癌的女性的家系。收集了这些女性所有一级亲属的癌症家族史,并将癌症发病率与省级年龄标准化发病率进行比较,以估计相对风险。在55岁以下的亲属中,共观察到82例癌症,而预期为31.2例,相对风险为2.6(95%置信区间(CI)2.1 - 3.3)。55岁以下患结直肠癌的相对风险为16.1(95%CI 11.6 - 21.8)。随着先证者癌症发病年龄的增加,这种风险降低。对于在55岁以下被诊断患有结直肠癌和子宫内膜癌的先证者,55岁以下亲属患结直肠癌的相对风险为30.5(95%CI 18.8 - 46.6)。子宫内膜癌和胰腺癌也观察到类似模式。食管癌、胃癌、小肠癌和膀胱癌的发病率有不显著的增加。乳腺癌风险没有增加。肺癌风险降低,尤其是老年亲属。我们的研究结果表明,患有结直肠癌和子宫内膜癌双原发癌的女性中存在显著的癌症遗传成分。