Nature Communications (Jun 2023)

Identification of BRCA1/2 mutation female carriers using circulating microRNA profiles

  • Kevin Elias,
  • Urszula Smyczynska,
  • Konrad Stawiski,
  • Zuzanna Nowicka,
  • James Webber,
  • Jakub Kaplan,
  • Charles Landen,
  • Jan Lubinski,
  • Asima Mukhopadhyay,
  • Dona Chakraborty,
  • Denise C. Connolly,
  • Heather Symecko,
  • Susan M. Domchek,
  • Judy E. Garber,
  • Panagiotis Konstantinopoulos,
  • Wojciech Fendler,
  • Dipanjan Chowdhury

DOI
https://doi.org/10.1038/s41467-023-38925-4
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 9

Abstract

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Abstract Identifying germline BRCA1/2 mutation carriers is vital for reducing their risk of breast and ovarian cancer. To derive a serum miRNA-based diagnostic test we used samples from 653 healthy women from six international cohorts, including 350 (53.6%) with BRCA1/2 mutations and 303 (46.4%) BRCA1/2 wild-type. All individuals were cancer-free before and at least 12 months after sampling. RNA-sequencing followed by differential expression analysis identified 19 miRNAs significantly associated with BRCA mutations, 10 of which were ultimately used for classification: hsa-miR-20b-5p, hsa-miR-19b-3p, hsa-let-7b-5p, hsa-miR-320b, hsa-miR-139-3p, hsa-miR-30d-5p, hsa-miR-17-5p, hsa-miR-182-5p, hsa-miR-421, hsa-miR-375-3p. The final logistic regression model achieved area under the receiver operating characteristic curve 0.89 (95% CI: 0.87–0.93), 93.88% sensitivity and 80.72% specificity in an independent validation cohort. Mutated gene, menopausal status or having preemptive oophorectomy did not affect classification performance. Circulating microRNAs may be used to identify BRCA1/2 mutations in patients of high risk of cancer, offering an opportunity to reduce screening costs.