| Literature DB >> 26171207 |
Yoshiaki Shinden1, Tomohiro Iguchi2, Sayuri Akiyoshi3, Hiroki Ueo2, Masami Ueda2, Hidenari Hirata2, Shotaro Sakimura2, Ryutaro Uchi2, Yuki Takano2, Hidetoshi Eguchi2, Keishi Sugimachi2, Yuko Kijima4, Shoji Natsugoe4, Koshi Mimori2.
Abstract
MicroRNA-29b (miR-29b) targets numerous important genes that mediate carcinogenesis and tumor development in breast cancer in vitro and in vivo. The aim of the present study was to determine the clinical significance of miR-29b expression in primary breast cancer patients. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) of miR-29b and certain target genes of miR-29b, such as DNA methyltransferase 3A (DNMT3A), ten-eleven translocation 1 (TET1) and thymine DNA glycosylase (TDG), was performed in 94 primary breast cancer samples. Low expression of miR-29b in primary tumors was significantly associated with poorer disease-free survival (DFS) (P=0.0075) and overall survival (OS) (p=0.0012). Multivariate analysis indicated that miR-29b expression was an independent prognostic factor for OS [relative risk=15.6 (2.33-348), P=0.0026]. In addition, a significant inverse correlation was identified between the expression levels of DNMT3A and miR-29b in estrogen receptor-positive breast cancer patients (P=0.027). To the best of our knowledge, this is the first study to investigate the clinicopathological significance of miR-29b in breast cancer cases and miR-29b is shown to act as a tumor suppressive microRNA in breast cancer and as a potential marker for recurrence and metastasis in breast cancer patients.Entities:
Keywords: DNA methyltransferase 3A; breast cancer; clinicopathological significance; microRNA-29b; prognosis
Year: 2015 PMID: 26171207 PMCID: PMC4486821 DOI: 10.3892/mco.2015.565
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450