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Expression of regulatory factor X1 can predict the prognosis of breast cancer.

Authors :
MASAHIRO SHIBATA
MITSURO KANDA
DAI SHIMIZU
HARUYOSHI TANAKA
SHINICHI UMEDA
MASAMICHI HAYASHI
TAKAHIRO INAISHI
NORIYUKI MIYAJIMA
YAYOI ADACHI
YUKO TAKANO
KENICHI NAKANISHI
DAI TAKEUCHI
SUMIYO NODA
YASUHIRO KODERA
TOYONE KIKUMORI
Source :
Oncology Letters. Jun2017, Vol. 13 Issue 6, p4334-4340. 7p.
Publication Year :
2017

Abstract

Breast cancer (BC) is the most common malignancy among women. Identifying novel biomarkers to predict prognosis accurately is important in managing this disease. The regulatory factor X1 (RFX1) gene is a member of the regulatory factor X gene family. Its protein reportedly downregulates the proto-oncogene c-myc, but its role in BC has been unclear. In this study, expression and methylation status of RFX1 were determined in BC cell lines. We then evaluated RFX1 mRNA expression levels with regard to clinicopathological factors including postoperative prognosis in 167 patients with BC. Expression of RFX1 was heterogeneous among cell lines, and we found no DNA methylation at the RFX1 promoter region. Patients were categorized into groups with high or low RFX1 expression, based on ratio of RFX1 mRNA expression in BC and adjacent non-cancerous tissues. The high RFX1 group was significantly associated with low T factor (P=0.028), earlier disease stage (P=0.015), positive expression of estrogen receptor (P=0.005) and progesterone receptor (P=0.011), negative expression of human epidermal growth factor receptor 2 (P=0.001). The high RFX1 group experienced more favorable disease-free survival (P=0.007) and overall survival (P=0.013). In multivariate analysis, RFX1 expression was an independent prognostic factor for disease-free survival. Our findings indicate that RFX1 may serve as a prognostic marker for BC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17921074
Volume :
13
Issue :
6
Database :
Academic Search Index
Journal :
Oncology Letters
Publication Type :
Academic Journal
Accession number :
123110820
Full Text :
https://doi.org/10.3892/ol.2017.6005