학술논문

Low FOXA1 expression predicts good response to neo-adjuvant chemotherapy resulting in good outcomes for luminal HER2-negative breast cancer cases.
Document Type
Article
Source
British Journal of Cancer. 1/20/2015, Vol. 112 Issue 2, p345-351. 7p. 5 Charts, 2 Graphs.
Subject
*FORKHEAD transcription factors
*GENE expression
*CANCER chemotherapy
*EPIDERMAL growth factor receptors
*BREAST cancer
*HORMONE therapy
*BIOMARKERS
Language
ISSN
0007-0920
Abstract
Background:FOXA1 expression is a good prognostic marker for endocrine therapy in hormone-positive breast cancer. We retrospectively examined breast cancer patients with luminal human epidermal growth factor receptor 2 (HER2)-negative tumours, as defined by immunohistochemistry, who received neo-adjuvant chemotherapy (NAC) and investigated the relationship between treatment effects and FOXA1 expression.Methods:Biopsy specimens from 103 luminal HER2-negative tumours were immunohistochemically examined. FOXA1 effects on chemo-sensitivity were also investigated employing in vitro experiments.Results:FOXA1 and Ki67 expressions independently predicted a pathological complete response (pCR). Knockdown of FOXA1 by siRNA boosted the chemo-effect in oestrogen receptor-positive cells. The Cox hazards model revealed a pCR to be the strongest factor predicting a good patient outcome.Conclusions:Our present study showed low FOXA1 expression to be associated with a good response to NAC in luminal HER2-negative breast cancer. Improved outcomes of these patients suggest that NAC should be recommended to patients with low FOXA1 tumours. [ABSTRACT FROM AUTHOR]