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Tumor Biological Features of BRCA1-Induced Breast Cancer

Johannsson, Oscar Thor ; Idvall, Ingrid LU ; Andersson, C. ; Borg, Åke LU ; Barkardóttir, R.B. ; Egilsson, V. and Olsson, Håkan LU orcid (1997) In European Journal of Cancer 33(3). p.362-371
Abstract
BRCA1 mutations, although implicated in disease predisposition in a major part of the hereditary breast cancer population, do not seem to be crucially involved in tumorigenesis of sporadic breast and ovarian cancers. This suggests that tumours arising in BRCA1 mutation carriers may differ from BRCA1 negative hereditary and sporadic cancer in genetic and biological features, as well as in clinical behaviour. Prior to BRCA1 analysis, 79 breast and 19 ovarian tumours from 57 breast and breast-ovarian cancer families, and 170 tumours from a comparison group of stage II breast cancers were studied with regard to histopathological features; immunohistochemistry [c-erbB-2, p53, oestrogen receptor (ER) and progesterone receptor (PR)], DNA flow... (More)
BRCA1 mutations, although implicated in disease predisposition in a major part of the hereditary breast cancer population, do not seem to be crucially involved in tumorigenesis of sporadic breast and ovarian cancers. This suggests that tumours arising in BRCA1 mutation carriers may differ from BRCA1 negative hereditary and sporadic cancer in genetic and biological features, as well as in clinical behaviour. Prior to BRCA1 analysis, 79 breast and 19 ovarian tumours from 57 breast and breast-ovarian cancer families, and 170 tumours from a comparison group of stage II breast cancers were studied with regard to histopathological features; immunohistochemistry [c-erbB-2, p53, oestrogen receptor (ER) and progesterone receptor (PR)], DNA flow cytometry and S-phase fraction. BRCA1 mutations were found in 40 breast and 15 ovarian tumours. The BRCA1 positive breast tumours were significantly more often of ductal type, histological grade III and manifested a heavy lymphocyte infiltration. Additionally, as compared to BRCA1 negative tumours, the BRCA1 positive tumours were significantly more often ER, PgR and c-erbB-2 negative. Furthermore, they were significantly more often DNA non-diploid, as well as being characterised by higher S-phase fraction values. These results suggest that BRCA1-induced breast cancers may manifest distinct tumour biological features of clinical importance. (Less)
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author
; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
c-erbB-2, ER, immunohistochemistry, histopathology, ovarian carcinoma, breast carcinoma, BRCA1, hereditary neoplasm, TP53, tumour infiltration
in
European Journal of Cancer
volume
33
issue
3
pages
362 - 371
publisher
Elsevier
external identifiers
  • scopus:0031105976
ISSN
1879-0852
DOI
10.1016/S0959-8049(97)89007-7
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Pathology, (Lund) (013030000), Oncology, MV (013035000)
id
f9053d34-39d5-4706-acda-832cff4d07ae (old id 34140)
date added to LUP
2016-04-01 16:47:37
date last changed
2022-04-07 18:43:48
@article{f9053d34-39d5-4706-acda-832cff4d07ae,
  abstract     = {{BRCA1 mutations, although implicated in disease predisposition in a major part of the hereditary breast cancer population, do not seem to be crucially involved in tumorigenesis of sporadic breast and ovarian cancers. This suggests that tumours arising in BRCA1 mutation carriers may differ from BRCA1 negative hereditary and sporadic cancer in genetic and biological features, as well as in clinical behaviour. Prior to BRCA1 analysis, 79 breast and 19 ovarian tumours from 57 breast and breast-ovarian cancer families, and 170 tumours from a comparison group of stage II breast cancers were studied with regard to histopathological features; immunohistochemistry [c-erbB-2, p53, oestrogen receptor (ER) and progesterone receptor (PR)], DNA flow cytometry and S-phase fraction. BRCA1 mutations were found in 40 breast and 15 ovarian tumours. The BRCA1 positive breast tumours were significantly more often of ductal type, histological grade III and manifested a heavy lymphocyte infiltration. Additionally, as compared to BRCA1 negative tumours, the BRCA1 positive tumours were significantly more often ER, PgR and c-erbB-2 negative. Furthermore, they were significantly more often DNA non-diploid, as well as being characterised by higher S-phase fraction values. These results suggest that BRCA1-induced breast cancers may manifest distinct tumour biological features of clinical importance.}},
  author       = {{Johannsson, Oscar Thor and Idvall, Ingrid and Andersson, C. and Borg, Åke and Barkardóttir, R.B. and Egilsson, V. and Olsson, Håkan}},
  issn         = {{1879-0852}},
  keywords     = {{c-erbB-2; ER; immunohistochemistry; histopathology; ovarian carcinoma; breast carcinoma; BRCA1; hereditary neoplasm; TP53; tumour infiltration}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{362--371}},
  publisher    = {{Elsevier}},
  series       = {{European Journal of Cancer}},
  title        = {{Tumor Biological Features of BRCA1-Induced Breast Cancer}},
  url          = {{http://dx.doi.org/10.1016/S0959-8049(97)89007-7}},
  doi          = {{10.1016/S0959-8049(97)89007-7}},
  volume       = {{33}},
  year         = {{1997}},
}