一些罕见癌症的高家族性风险可能指向隐藏的生殖系遗传:重点关注食管癌、胃癌、小肠、睾丸癌、甲状腺癌和骨癌。

IF 2 4区 医学 Q3 ONCOLOGY
Kari Hemminki, Otto Hemminki, Anni Koskinen, Akseli Hemminki, Asta Försti
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引用次数: 0

摘要

背景:罕见的食道癌、胃癌、小肠癌、睾丸癌、(非髓质)甲状腺癌和骨癌的种系遗传易感性尚不清楚,具有较高的家族性风险。在这里,我们使用来自瑞典家庭癌症数据库的家族风险数据,该数据库包含了一个多世纪以来瑞典家庭的癌症记录。我们比较了父母是否患有这些癌症时,被诊断患有这些癌症的后代的家族风险。我们回顾了全球文献报道的体质变异,可能解释部分家族风险。主体:食管癌和胃癌的家族性风险约为2.0,除早发性胃癌外,已知的高危变异体很少。遗传研究可能受到这些癌症的主要环境风险因素的阻碍。小肠类癌具有非常高的家族性风险(兄弟姐妹之间的风险为28),但没有发现高风险基因来解释这一现象。已经发现了低风险的多基因变异。小肠腺癌是Lynch综合征的一种表现。尽管甲状腺癌是一些罕见癌症综合征的组成部分,但睾丸癌和甲状腺癌的特点是家族性风险高(约5),这在很大程度上可以解释为多基因背景。已经确定了几个骨癌的易感基因(家族性风险7)。结论:尽管缺乏确定的高渗透体质变异,但所讨论的癌症是罕见的,它们具有相对较高的家族性风险。这可能是多基因成分,已经被认为是睾丸癌,比以前预期的更强。因此,具有罕见的高/中等和低风险变异的多基因模型可以适应家族风险并塑造这些癌症的种系遗传景观。多基因背景可能具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High familial risks in some rare cancers may pinpoint to hidden germline genetics: focus on esophageal, stomach, small intestinal, testis, thyroid and bone cancers.

Background: Germline genetic susceptibilities of rare cancers of the esophagus, stomach, small intestine, testis, (nonmedullary) thyroid gland and bone with high familial risks are not well known. Here, we use familial risk data from the Swedish Family-Cancer Database which contains records of cancers in Swedish families obtained over a century. We compare familial risks for offspring diagnosed with any of these cancers when their parent had or had not that cancer. We review the global literature of the reported constitutional variants that may explain part of the familial risk.

Main body: Familial risks for esophageal and stomach cancers are about 2.0 and apart from early-onset stomach cancer few high-risk variants are known. Genetic studies may be hampered by dominant environmental risk factors for these cancers. Small intestinal carcinoids have a very high familial risk (28 between siblings) but no high-risk genes have been identified to explain this. Low-risk polygenic variants have been identified. Small intestinal adenocarcinoma is a manifestation in Lynch syndrome. Testicular and thyroid cancers are characterized by high familial risk (about 5) which may be explained largely by a polygenic background, although thyroid cancer is a component in a number of rare cancer syndromes. Several predisposing genes have been identified for bone cancer (familial risk 7).

Conclusions: The discussed cancers are rare and they present with a relatively high familial risk, in spite of lacking identified high-penetrant constitutional variants. It is possible that the polygenic component, already recognized for testis cancer, is stronger than previously expected. Thus polygenic models with rare high/moderate- and low-risk variants could fit the familial risk and shape the germline genetic landscape of these cancers. Polygenic background may have clinical implications.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
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