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Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33.

Authors :
Webster LR
Provan PJ
Graham DJ
Byth K
Walker RL
Davis S
Salisbury EL
Morey AL
Ward RL
Hawkins NJ
Clarke CL
Meltzer PS
Balleine RL
Source :
Pathology [Pathology] 2013 Dec; Vol. 45 (7), pp. 629-36.
Publication Year :
2013

Abstract

Aims: In a study of ductal carcinoma in situ of the breast, we identified five genes at chromosome 17q21.33 that were over-expressed in high grade cases, and showed a correlation between expression and gene copy number. The aim of this study was to investigate potential drivers of genomic amplification at 17q21.33.<br />Methods: Analysis of high resolution comparative genomic hybridisation and published data specified a minimum region of amplification at 17q21.33. Prohibitin (PHB) expression was examined by immunohistochemistry in 285 invasive breast cancers. Gene copy number was examined by fluorescence in situ hybridisation.<br />Results: The minimum region of amplification at 17q21.33 included ten genes with PHB selected as a candidate driver. Increased PHB expression was associated with higher grade breast cancer and poorer survival. Amplification of PHB was detected in 13 of 235 cases (5.5%) but was not associated with PHB expression. PHB amplification was most common in the ERBB2+ breast cancer subtype, although high expression was most prevalent in basal-like and luminal B cancers.<br />Conclusions: Amplification at 17q21.33 is a recurrent feature of breast cancer that forms part of a 'firestorm' pattern of genomic aberration. PHB is not a driver of amplification, however PHB may contribute to high grade breast cancer.

Details

Language :
English
ISSN :
1465-3931
Volume :
45
Issue :
7
Database :
MEDLINE
Journal :
Pathology
Publication Type :
Academic Journal
Accession number :
24247619
Full Text :
https://doi.org/10.1097/PAT.0000000000000004