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Clonal relationships between lobular carcinoma in situ and other breast malignancies

Authors :
Victor P. Andrade
Rita A. Sakr
Dilip Giri
Irina Ostrovnaya
Colin B. Begg
Marina De Brot
Michail Schizas
Russell Towers
Venkatraman E. Seshan
Tari A. King
Audrey Mauguen
Jose V. Scarpa Carniello
Source :
Breast Cancer Research : BCR
Publication Year :
2016
Publisher :
Springer Science and Business Media LLC, 2016.

Abstract

Background Recent evidence suggests that lobular carcinoma in situ (LCIS) can be a clonal precursor of invasive breast cancers of both the ductal and lobular phenotypes. We sought to confirm these findings with an extensive study of fresh frozen breast specimens from women undergoing mastectomy. Methods Patients with a history of LCIS presenting for therapeutic mastectomy were identified prospectively. Frozen tissue blocks were collected, screened for lesions of interest, and subjected to microdissection and DNA extraction. Copy number profiling, whole-exome sequencing, or both were performed. Clonal relatedness was assessed using specialized statistical techniques developed for this purpose. Results After exclusions for genotyping failure, a total of 84 lesions from 30 patients were evaluated successfully. Strong evidence of clonal relatedness was observed between an LCIS lesion and the invasive cancer for the preponderance of cases with lobular carcinoma. Anatomically distinct in situ lesions of both ductal and lobular histology were also shown to be frequently clonally related. Conclusions These data derived from women with LCIS with or without invasive cancer confirm that LCIS is commonly the clonal precursor of invasive lobular carcinoma and that distinct foci of LCIS frequently share a clonal origin, as do foci of LCIS and ductal carcinoma in situ. Electronic supplementary material The online version of this article (doi:10.1186/s13058-016-0727-z) contains supplementary material, which is available to authorized users.

Details

ISSN :
1465542X
Volume :
18
Database :
OpenAIRE
Journal :
Breast Cancer Research
Accession number :
edsair.doi.dedup.....2f5538dab021397d60f6dce07c382bca
Full Text :
https://doi.org/10.1186/s13058-016-0727-z