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Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer.

Publication ,  Journal Article
Song, H; Dicks, EM; Tyrer, J; Intermaggio, M; Chenevix-Trench, G; Bowtell, DD; Traficante, N; Group, A; Brenton, J; Goranova, T; Hosking, K ...
Published in: J Med Genet
May 2021

PURPOSE: The known epithelial ovarian cancer (EOC) susceptibility genes account for less than 50% of the heritable risk of ovarian cancer suggesting that other susceptibility genes exist. The aim of this study was to evaluate the contribution to ovarian cancer susceptibility of rare deleterious germline variants in a set of candidate genes. METHODS: We sequenced the coding region of 54 candidate genes in 6385 invasive EOC cases and 6115 controls of broad European ancestry. Genes with an increased frequency of putative deleterious variants in cases versus controls were further examined in an independent set of 14 135 EOC cases and 28 655 controls from the Ovarian Cancer Association Consortium and the UK Biobank. For each gene, we estimated the EOC risks and evaluated associations between germline variant status and clinical characteristics. RESULTS: The ORs associated for high-grade serous ovarian cancer were 3.01 for PALB2 (95% CI 1.59 to 5.68; p=0.00068), 1.99 for POLK (95% CI 1.15 to 3.43; p=0.014) and 4.07 for SLX4 (95% CI 1.34 to 12.4; p=0.013). Deleterious mutations in FBXO10 were associated with a reduced risk of disease (OR 0.27, 95% CI 0.07 to 1.00, p=0.049). However, based on the Bayes false discovery probability, only the association for PALB2 in high-grade serous ovarian cancer is likely to represent a true positive. CONCLUSIONS: We have found strong evidence that carriers of PALB2 deleterious mutations are at increased risk of high-grade serous ovarian cancer. Whether the magnitude of risk is sufficiently high to warrant the inclusion of PALB2 in cancer gene panels for ovarian cancer risk testing is unclear; much larger sample sizes will be needed to provide sufficiently precise estimates for clinical counselling.

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Published In

J Med Genet

DOI

EISSN

1468-6244

Publication Date

May 2021

Volume

58

Issue

5

Start / End Page

305 / 313

Location

England

Related Subject Headings

  • Risk Assessment
  • Ovarian Neoplasms
  • Humans
  • Genetics & Heredity
  • Genetic Variation
  • Genetic Predisposition to Disease
  • Female
  • Fanconi Anemia Complementation Group N Protein
  • Case-Control Studies
  • 3202 Clinical sciences
 

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Song, H., Dicks, E. M., Tyrer, J., Intermaggio, M., Chenevix-Trench, G., Bowtell, D. D., … Pharoah, P. (2021). Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer. J Med Genet, 58(5), 305–313. https://doi.org/10.1136/jmedgenet-2019-106739
Song, Honglin, Ed M. Dicks, Jonathan Tyrer, Maria Intermaggio, Georgia Chenevix-Trench, David D. Bowtell, Nadia Traficante, et al. “Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer.J Med Genet 58, no. 5 (May 2021): 305–13. https://doi.org/10.1136/jmedgenet-2019-106739.
Song H, Dicks EM, Tyrer J, Intermaggio M, Chenevix-Trench G, Bowtell DD, et al. Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer. J Med Genet. 2021 May;58(5):305–13.
Song, Honglin, et al. “Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer.J Med Genet, vol. 58, no. 5, May 2021, pp. 305–13. Pubmed, doi:10.1136/jmedgenet-2019-106739.
Song H, Dicks EM, Tyrer J, Intermaggio M, Chenevix-Trench G, Bowtell DD, Traficante N, Group A, Brenton J, Goranova T, Hosking K, Piskorz A, van Oudenhove E, Doherty J, Harris HR, Rossing MA, Duerst M, Dork T, Bogdanova NV, Modugno F, Moysich K, Odunsi K, Ness R, Karlan BY, Lester J, Jensen A, Krüger Kjaer S, Høgdall E, Campbell IG, Lázaro C, Pujara MA, Cunningham J, Vierkant R, Winham SJ, Hildebrandt M, Huff C, Li D, Wu X, Yu Y, Permuth JB, Levine DA, Schildkraut JM, Riggan MJ, Berchuck A, Webb PM, Group OS, Cybulski C, Gronwald J, Jakubowska A, Lubinski J, Alsop J, Harrington P, Chan I, Menon U, Pearce CL, Wu AH, de Fazio A, Kennedy CJ, Goode E, Ramus S, Gayther S, Pharoah P. Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer. J Med Genet. 2021 May;58(5):305–313.

Published In

J Med Genet

DOI

EISSN

1468-6244

Publication Date

May 2021

Volume

58

Issue

5

Start / End Page

305 / 313

Location

England

Related Subject Headings

  • Risk Assessment
  • Ovarian Neoplasms
  • Humans
  • Genetics & Heredity
  • Genetic Variation
  • Genetic Predisposition to Disease
  • Female
  • Fanconi Anemia Complementation Group N Protein
  • Case-Control Studies
  • 3202 Clinical sciences