TY - JOUR
T1 - Molecular alterations in metaplastic breast carcinoma
AU - Cooper, Caroline L.
AU - Karim, Rooshdiya Z.
AU - Selinger, Christina
AU - Carmalt, Hugh
AU - Lee, C. Soon
AU - O'Toole, Sandra A.
PY - 2013
Y1 - 2013
N2 - Metaplastic carcinoma of the breast is a rare and heterogeneous subtype of breast carcinoma with a generally poor outcome, and few therapeutic options once disease recurs or progresses. Metaplastic carcinomas of the breast are usually of a larger size at diagnosis, with less frequent nodal metastasis compared with invasive ductal carcinoma no special type, and lack hormone and HER2 receptor expression. Recent research has revealed some potentially actionable genetic changes in a subset of these rare tumours. However, ongoing efforts to further characterise the genetic basis and the molecular alterations underlying the distinctive morphological and clinical characteristics of these tumours are needed in order to identify new targets for treatment. This review will describe the theories of pathogenesis of metaplastic breast carcinoma, and highlight genetic changes and potential therapeutic targets in this generally poor prognosis malignancy.
AB - Metaplastic carcinoma of the breast is a rare and heterogeneous subtype of breast carcinoma with a generally poor outcome, and few therapeutic options once disease recurs or progresses. Metaplastic carcinomas of the breast are usually of a larger size at diagnosis, with less frequent nodal metastasis compared with invasive ductal carcinoma no special type, and lack hormone and HER2 receptor expression. Recent research has revealed some potentially actionable genetic changes in a subset of these rare tumours. However, ongoing efforts to further characterise the genetic basis and the molecular alterations underlying the distinctive morphological and clinical characteristics of these tumours are needed in order to identify new targets for treatment. This review will describe the theories of pathogenesis of metaplastic breast carcinoma, and highlight genetic changes and potential therapeutic targets in this generally poor prognosis malignancy.
UR - http://handle.uws.edu.au:8081/1959.7/530067
U2 - 10.1136/jclinpath-2012-201086
DO - 10.1136/jclinpath-2012-201086
M3 - Article
SN - 0021-9746
VL - 66
SP - 522
EP - 528
JO - Journal of Clinical Pathology
JF - Journal of Clinical Pathology
IS - 6
ER -