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Status: Bibliographieeintrag

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Verfasst von:Zheng, Guoqiao [VerfasserIn]   i
 Catalano, Calogerina [VerfasserIn]   i
 Bandapalli, Obul Reddy [VerfasserIn]   i
 Paramasivam, Nagarajan [VerfasserIn]   i
 Chattopadhyay, Subhayan [VerfasserIn]   i
 Schlesner, Matthias [VerfasserIn]   i
 Sijmons, Rolf [VerfasserIn]   i
 Hemminki, Akseli [VerfasserIn]   i
 Dymerska, Dagmara [VerfasserIn]   i
 Lubinski, Jan [VerfasserIn]   i
 Hemminki, Kari [VerfasserIn]   i
 Försti, Asta [VerfasserIn]   i
Titel:Cancer predisposition genes in cancer-free families
Verf.angabe:Guoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, Nagarajan Paramasivam, Subhayan Chattopadhyay, Matthias Schlesner, Rolf Sijmons, Akseli Hemminki, Dagmara Dymerska, Jan Lubinski, Kari Hemminki and Asta Försti
E-Jahr:2020
Jahr:27 September 2020
Umfang:13 S.
Fussnoten:Gesehen am 30.11.2020
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2020
Band/Heft Quelle:12(2020,10) Artikel-Nummer 2770, 13 Seiten
ISSN Quelle:2072-6694
Abstract:Familial clustering, twin concordance, and identification of high- and low-penetrance cancer predisposition variants support the idea that there are families that are at a high to moderate excess risk of cancer. To what extent there may be families that are protected from cancer is unknown. We wanted to test genetically whether cancer-free families share fewer breast, colorectal, and prostate cancer risk alleles than the population at large. We addressed this question by whole-genome sequencing (WGS) of 51 elderly cancer-free individuals whose numerous (ca. 1000) family members were found to be cancer-free (‘cancer-free families’, CFFs) based on face-to-face interviews. The average coverage of the 51 samples in the WGS was 42x. We compared cancer risk allele frequencies in cancer-free individuals with those in the general population available in public databases. The CFF members had fewer loss-of-function variants in suggested cancer predisposition genes compared to the ExAC data, and for high-risk cancer predisposition genes, no pathogenic variants were found in CFFs. For common low-penetrance breast, colorectal, and prostate cancer risk alleles, the results were not conclusive. The results suggest that, in line with twin and family studies, random environmental causes are so dominant that a clear demarcation of cancer-free populations using genetic data may not be feasible.
DOI:doi:10.3390/cancers12102770
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.3390/cancers12102770
 Volltext: https://www.mdpi.com/2072-6694/12/10/2770
 DOI: https://doi.org/10.3390/cancers12102770
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:high-risk genes
 polygenic risk
 predisposing genes
 random environment
K10plus-PPN:174145509X
Verknüpfungen:→ Zeitschrift

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