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瑞典家族性癌症国家数据库。

National database of familial cancer in Sweden.

作者信息

Hemminki K, Vaittinen P

机构信息

Department of Biosciences, Karolinska Institute, Huddinge, Sweden.

出版信息

Genet Epidemiol. 1998;15(3):225-36. doi: 10.1002/(SICI)1098-2272(1998)15:3<225::AID-GEPI2>3.0.CO;2-3.

Abstract

A family cancer database was constructed from the nationwide Swedish registries and includes approximately 6 million persons and >30,000 cancers in offspring diagnosed at ages 15-51 years and their parents. A particular advantage of the database is that the contribution of both parental lineages on cancer risk can be examined. Cancer risk in the offspring was increased approximately 1.1 times when the father had cancer, and no increase was noted when the mother had cancer. If both parents had cancer, the risk for sons was 1.4 and for daughters 1.3. The sites of increased cancer risk in the offspring were colorectum, breast, cervix, corpus uteri, ovary, testis, melanoma, eye, other endocrine glands, and multiple myeloma. The results among young and middle-age adults suggest that cancer in both parents increases the cancer risk in the offspring at many sites. The molecular genetic explanation may be that rare dominant single genes increase susceptibility at many sites, or that overlapping sets of genes control susceptibility at multiple sites.

摘要

一个家族癌症数据库是根据瑞典全国性登记处的数据构建的,包含约600万人以及15至51岁的后代及其父母中确诊的3万多例癌症。该数据库的一个特别优势在于,可以研究父母双方的家族谱系对癌症风险的影响。当父亲患癌症时,后代患癌风险大约增加1.1倍,而母亲患癌时则未观察到风险增加。如果父母双方都患癌症,儿子的风险为1.4,女儿的风险为1.3。后代患癌风险增加的部位包括结肠直肠、乳腺、子宫颈、子宫体、卵巢、睾丸、黑色素瘤、眼睛、其他内分泌腺以及多发性骨髓瘤。青年和中年成年人的研究结果表明,父母双方患癌会增加后代多个部位的患癌风险。分子遗传学解释可能是,罕见的显性单基因会增加多个部位的易感性,或者是重叠的基因组合控制着多个部位的易感性。

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