Literature DB >> 27986439

Expression Levels of KMT2C and SLC20A1 Identified by Information-theoretical Analysis Are Powerful Prognostic Biomarkers in Estrogen Receptor-positive Breast Cancer.

Keiko Sato1, Kazunori Akimoto2.   

Abstract

INTRODUCTION: In general, it has been considered that estrogen receptor-positive (ER+) breast cancer has a good prognosis and is responsive to endocrine therapy. However, one third of patients with ER+ breast cancer exhibit endocrine therapy resistance, and many patients develop recurrence and die 5 to 10 years after diagnosis. In ER+ breast cancer, a major problem is to distinguish those patients most likely to develop recurrence or metastatic disease within 10 years after diagnosis from those with a sufficiently good prognosis.
MATERIALS AND METHODS: We downloaded the messenger RNA expression data and the clinical information for 401 patients with ER+ breast cancer from the cBioPortal for Cancer Genomics. An information-theoretical approach was used to identify the prognostic factors for survival in patients with ER+ breast cancer and to classify those patients according to the prognostic factors.
RESULTS: The information-theoretical approach contributed to the identification of KMT2C and SLC20A1 as prognostic biomarkers in ER+ breast cancer. We found that low KMT2C expression was associated with a poor outcome and high SLC20A1 expression was associated with a poor outcome. Both levels of KMT2C and SLC20A1 expression were significantly and strongly associated with the differentiation of survival. The 10-year survival rate for ER+ patients with low KMT2C and high SLC20A1 expression was 0%. In contrast, for ER+ patients with high KMT2C and low SLC20A1 expression, the 10-year survival rate was 86.78%.
CONCLUSION: Our results strongly suggest that clinical examination of the expression of both KMT2C and SLC20A1 in ER+ breast cancer will be very useful for the determination of prognosis and therapy.
Copyright © 2016 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Classification; ER(+) breast cancer; Gene expression; Information theory; Prognosis

Mesh:

Substances:

Year:  2016        PMID: 27986439     DOI: 10.1016/j.clbc.2016.11.005

Source DB:  PubMed          Journal:  Clin Breast Cancer        ISSN: 1526-8209            Impact factor:   3.225


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