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| 001 | 274161 | ||
| 005 | 20240229154927.0 | ||
| 024 | 7 | _ | |a 10.1186/s13053-023-00247-3 |2 doi |
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| 024 | 7 | _ | |a 1731-2302 |2 ISSN |
| 024 | 7 | _ | |a 1897-4287 |2 ISSN |
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| 037 | _ | _ | |a DKFZ-2023-00463 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a Hemminki, Kari |0 P:(DE-He78)19b0ec1cea271419d9fa8680e6ed6865 |b 0 |e First author |u dkfz |
| 245 | _ | _ | |a Are population level familial risks and germline genetics meeting each other? |
| 260 | _ | _ | |a Heidelberg |c 2023 |b Springer |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1678271185_6777 |2 PUB:(DE-HGF) |x Review Article |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
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| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 500 | _ | _ | |a #EA:C020# |
| 520 | _ | _ | |a Large amounts of germline sequencing data have recently become available and we sought to compare these results with population-based family history data. Family studies are able to describe aggregation of any defined cancers in families. The Swedish Family-Cancer Database is the largest of its kind in the world, covering the Swedish families through nearly a century with all cancers in family members since the start of national cancer registration in 1958. The database allows estimation of familial risks, ages of cancer onset and the proportion of familial cancer in different family constellations. Here, we review the proportion of familial cancer for all common cancers and specify them based on the number of affected individuals. With the exception of a few cancers, age of onset of familial cancer is not different from all cancers combined. The highest proportions of familial cancer were found for prostate (26.4%), breast (17.5%) and colorectal (15.7%) cancers, but the proportions of high-risk families with multiple affected individuals were only 2.8%, 1% and 0.9%, respectively. A large sequencing study on female breast cancer found that BRCA1 and BRCA2 mutations could account for 2% of the cases (subtracting the proportions in healthy individuals) and that all germline mutations accounted for 5.6% of the cases. Early age of onset was a distinct feature of only BRCA mutations. In heritable colorectal cancer, Lynch syndrome genes dominate. Large studies on penetrance in Lynch syndrome have shown an approximately linear increase in risk from 40-50 years up to age 80 years. Interesting novel data revealed a strong modification of familial risk by unknown factors. High-risk germline genetics of prostate cancer is characterized by BRCA and other DNA repair genes. HOXB13 encodes a transcription factor which contributes to germline risk of prostate cancer. A strong interaction was shown with a polymorphism in the CIP2A gene. The emerging germline landscape of common cancers can be reasonably accommodated by family data on these cancers as to high-risk proportions and age of onset. |
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| 650 | _ | 7 | |a Familial proportion |2 Other |
| 650 | _ | 7 | |a Familial risk |2 Other |
| 650 | _ | 7 | |a Family-Cancer Database |2 Other |
| 650 | _ | 7 | |a High-risk families |2 Other |
| 650 | _ | 7 | |a Nation-wide study |2 Other |
| 700 | 1 | _ | |a Li, Xinjun |b 1 |
| 700 | 1 | _ | |a Försti, Asta |0 P:(DE-He78)f26164c08f2f14abcf31e52e13ee3696 |b 2 |u dkfz |
| 700 | 1 | _ | |a Eng, Charis |b 3 |
| 773 | _ | _ | |a 10.1186/s13053-023-00247-3 |g Vol. 21, no. 1, p. 3 |0 PERI:(DE-600)2233352-6 |n 1 |p 3 |t Hereditary cancer in clinical practice |v 21 |y 2023 |x 1731-2302 |
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