TY - JOUR
T1 - Therapeutic targets in triple negative breast cancer
AU - O'Toole, Sandra A.
AU - Beith, Jane M.
AU - Millar, Ewan K. A.
AU - West, Richard
AU - McLean, Anna
AU - Cazet, Aurelie
AU - Swarbrick, Alexander
AU - Oakes, Samantha R.
PY - 2013
Y1 - 2013
N2 - Outcomes have improved signi ficantly for many women diagnosed with breast cancer. For the heterogeneous group of tumours lacking expression of the oestrogen, progesterone and HER2 receptors, 'triple negative' breast cancers (TNBC), the prognosis overall has remained quite poor. When TNBC recurs, there is often little response to chemotherapy, and there are a few treatment options in this setting. Thus, there is an urgent clinical need to identify new therapeutic targets in order to improve the outlook for these patients. This review highlights the most promising therapeutic targets identified through new sequencing technologies, as well as through studies of apoptosis. We also present mounting evidence that the developmental signalling pathways Wnt/β-catenin, NOTCH and Hedgehog play an important role in the pathogenesis and progression of TNBC with new therapeutic approaches inhibiting these pathways in advanced preclinical studies or early clinical trials.
AB - Outcomes have improved signi ficantly for many women diagnosed with breast cancer. For the heterogeneous group of tumours lacking expression of the oestrogen, progesterone and HER2 receptors, 'triple negative' breast cancers (TNBC), the prognosis overall has remained quite poor. When TNBC recurs, there is often little response to chemotherapy, and there are a few treatment options in this setting. Thus, there is an urgent clinical need to identify new therapeutic targets in order to improve the outlook for these patients. This review highlights the most promising therapeutic targets identified through new sequencing technologies, as well as through studies of apoptosis. We also present mounting evidence that the developmental signalling pathways Wnt/β-catenin, NOTCH and Hedgehog play an important role in the pathogenesis and progression of TNBC with new therapeutic approaches inhibiting these pathways in advanced preclinical studies or early clinical trials.
UR - http://handle.uws.edu.au:8081/1959.7/530056
U2 - 10.1136/jclinpath-2012-201361
DO - 10.1136/jclinpath-2012-201361
M3 - Article
SN - 0021-9746
VL - 66
SP - 530
EP - 542
JO - Journal of Clinical Pathology
JF - Journal of Clinical Pathology
IS - 6
ER -