Combined annotation‐dependent depletion score for BRCA1/2 variants in patients with breast and/or ovarian cancer. Issue 2 (17th January 2018)
- Record Type:
- Journal Article
- Title:
- Combined annotation‐dependent depletion score for BRCA1/2 variants in patients with breast and/or ovarian cancer. Issue 2 (17th January 2018)
- Main Title:
- Combined annotation‐dependent depletion score for BRCA1/2 variants in patients with breast and/or ovarian cancer
- Authors:
- Nakagomi, Hiroshi
Mochizuki, Hitoshi
Inoue, Masayuki
Hirotsu, Yosuke
Amemiya, Kenji
Sakamoto, Ikuko
Nakagomi, Satoko
Kubota, Takeo
Omata, Masao - Abstract:
- Abstract : Utility of combined annotation‐dependent depletion (CADD) score was recently reported to rank pathogenicity as C‐scores ranging 1‐99 for both confirmed deleterious mutation. Using C‐scores for BRCA1/2 variants, we tried to constitute the classification system for variant of uncertain significance (VUS), which had been a major problem of genetic testing for hereditary breast and/or ovarian cancer. We analyzed BRCA1/2 genes for 283 patients with breast and/or ovarian cancer. The deleterious mutation and missesne mutations, minor variant, and wild type of BRCA1 and ‐ 2 were 5, 27, 251 and 15, 85, 183, respectively. Meanwhile, the variants with C‐score ≥10 were involved in 19/283 (6.7%) in BRCA1 and 34/283 (12%) in BRCA2 . All deleterious mutations were included in this group. Frequency of personal history and family history of ovarian cancer were significantly high, and frequency of serous adenocarcinoma of ovary and triple negative breast cancer was relatively high in the group with deleterious mutations. Similar findings were seen in patients with variants of C‐score ≥10. According to the C‐score and population frequency, we could define VUS for 11 patients out of 283 patients (3.9 CADD is useful to classify the variant of BRCA1/2 and selecting the patient who needs further segregation studies. Abstract : Combined annotation‐dependent depletion (CADD) score is useful to classify BRCA1/2 variants in patients with breast and/or ovarian cancer.
- Is Part Of:
- Cancer science. Volume 109:Issue 2(2018)
- Journal:
- Cancer science
- Issue:
- Volume 109:Issue 2(2018)
- Issue Display:
- Volume 109, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 109
- Issue:
- 2
- Issue Sort Value:
- 2018-0109-0002-0000
- Page Start:
- 453
- Page End:
- 461
- Publication Date:
- 2018-01-17
- Subjects:
- BRCA -- combined annotation‐dependent depletion -- genetic counseling -- hereditary breast and/or ovarian cancer -- variant of uncertain significance
Cancer -- Periodicals
Neoplasms -- Periodicals
Research -- Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1347-9032;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cas.13464 ↗
- Languages:
- English
- ISSNs:
- 1347-9032
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.603000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9704.xml