| Literature DB >> 26000816 |
Qing Ouyang1, Lunshan Xu1, Hongjuan Cui2, Minhui Xu1, Liang Yi1.
Abstract
The control of malignant glioma cell cycle by microRNAs (miRNAs) is well established. The deregulation of miRNAs in glioma may contribute to tumor proliferation by directly targeting the critical cell-cycle regulators. Tumor suppressive miRNAs inhibit cell cycle through repressing the expression of positive cell-cycle regulators. However, oncogenic miRNAs promote the cell-cycle progression by targeting cell-cycle negative regulators. Recent studies have identified that transcription factors had involved in the expression of miRNAs. Transcription factors and miRNAs are implicated in regulatory network of glioma cell cycle, the deregulation of these transcription factors might be a cause of the deregulation of miRNAs. Abnormal versions of miRNAs have been implicated in the cell cycle of glioma. Based on those, miRNAs are excellent biomarker candidates and potential targets for therapeutic intervention in glioma.Entities:
Keywords: Glioma; biomarkers; cell cycle; microRNAs; transcription factor
Mesh:
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Year: 2015 PMID: 26000816 DOI: 10.3109/00207454.2015.1017881
Source DB: PubMed Journal: Int J Neurosci ISSN: 0020-7454 Impact factor: 2.292