Abstract
It has been reported that miR-22 plays an important role and may be a promising therapeutic target in cancer. In this study, we found that GLUT1 is a direct target of miR-22. The ectopic expression of miR-22 inhibited breast cancer cell proliferation and invasion by targeting GLUT1. A reverse correlation between the expression of miR-22 and GLUT1 was observed in breast cancer tissue samples. Furthermore, miR-22 was significantly correlated with the TNM stage, local relapse, distant metastasis, and survival of breast cancer patients. Our data suggest that miR-22 functions as a tumor suppressor and is a promising prognostic biomarker in breast cancer.
Keywords:
Breast cancer; GLUT1; Prognostic factor; miR-22.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Apoptosis
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Blotting, Western
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Breast Neoplasms / genetics*
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Breast Neoplasms / metabolism
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Breast Neoplasms / mortality
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Breast Neoplasms / pathology
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Cell Movement
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Cell Proliferation
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Female
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Gene Expression Regulation, Neoplastic*
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Glucose Transporter Type 1 / antagonists & inhibitors
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Glucose Transporter Type 1 / genetics
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Glucose Transporter Type 1 / metabolism*
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Humans
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Immunoenzyme Techniques
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MicroRNAs / genetics*
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Middle Aged
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Neoplasm Invasiveness
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Neoplasm Recurrence, Local / genetics*
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Neoplasm Recurrence, Local / metabolism
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Neoplasm Recurrence, Local / mortality
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Neoplasm Recurrence, Local / pathology
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Neoplasm Staging
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Prognosis
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RNA, Messenger / genetics
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RNA, Small Interfering / genetics
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Real-Time Polymerase Chain Reaction
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Reverse Transcriptase Polymerase Chain Reaction
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Survival Rate
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Tumor Cells, Cultured
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Tumor Stem Cell Assay
Substances
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Glucose Transporter Type 1
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MIRN22 microRNA, human
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MicroRNAs
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RNA, Messenger
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RNA, Small Interfering
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SLC2A1 protein, human