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. 2023 Nov-Dec;37(6):2473-2479.
doi: 10.21873/invivo.13354.

Expression of miRNA-451 and miRNA-885 in Meningiomas

Affiliations

Expression of miRNA-451 and miRNA-885 in Meningiomas

Ozgur Baran et al. In Vivo. 2023 Nov-Dec.

Abstract

Background/aim: Meningiomas are one of the most common intracranial tumors, accounting for 30% of the tumors of the central nervous system. MicroRNAs (miRNAs) are noncoding RNAs containing approximately 18-22 nucleotides that regulate gene expression by interfering with transcription or inhibiting translation. Recent studies have reported that miRNAs could provide information about the molecular pathogenesis of several types of tumors. This study aimed to examine the expression levels of miRNA-885 and -451 and to determine their potential roles as biomarkers in meningioma.

Materials and methods: In total, 29 patients with meningioma (9 males and 20 females) were included in this study. The expression levels of miRNA were determined using real-time polymerase chain reaction. In addition, receiver operating characteristic curve analysis was used to analyze the predictive potential of miRNAs.

Results: Our results indicated a significant increase in miRNA-451 expression levels (p=0.003); however, there was no significant change in miRNA-885 expression levels (p=0.139) in patients with meningioma compared with the control group. Moreover, miRNA-885 and miRNA-451 expression levels did not differ significantly based on the histopathological grade of meningioma.

Conclusion: miRNA-451 may be a novel potential marker for the diagnosis and prognosis, and a target for meningioma treatment.

Keywords: Meningiomas; gene expression; microRNA-451; microRNA-885; neuro-oncology.

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Conflict of interest statement

The Authors declare that they have no conflicts of interest regarding the publication of this article.

Figures

Figure 1
Figure 1. Comparison of miRNA-885 expression levels between the meningioma and control groups. Differences between the two groups were analyzed using the Mann-Whitney U-test. *p-value <0.05.
Figure 2
Figure 2. Comparison of miRNA-451 expression levels between the meningioma and control groups based on fold change. Differences between the two groups were analyzed using the Mann-Whitney U-test. *p-value <0.05.
Figure 3
Figure 3. ROC analysis graph of miRNA-451 expression levels in the control and meningioma groups. *p-value <0.05.

References

    1. Ostrom QT, Gittleman H, Truitt G, Boscia A, Kruchko C, Barnholtz-Sloan JS. CBTRUS statistical report: Primary brain and other central nervous system tumors diagnosed in the United States in 2011-2015. Neuro Oncol. 2018;20(suppl_4):iv1–iv86. doi: 10.1093/neuonc/noy131. - DOI - PMC - PubMed
    1. Mahmood A, Caccamo DV, Tomecek FJ, Malik GM. Atypical and malignant meningiomas. Neurosurgery. 1993;33(6):955–963. doi: 10.1227/00006123-199312000-00001. - DOI - PubMed
    1. Marciscano AE, Stemmer-Rachamimov AO, Niemierko A, Larvie M, Curry WT, Barker FG 2nd, Martuza RL, McGuone D, Oh KS, Loeffler JS, Shih HA. Benign meningiomas (WHO Grade I) with atypical histological features: correlation of histopathological features with clinical outcomes. J Neurosurg. 2016;124(1):106–114. doi: 10.3171/2015.1.JNS142228. - DOI - PubMed
    1. Hortobágyi T, Bencze J, Varkoly G, Kouhsari MC, Klekner Á. Meningioma recurrence. Open Med (Wars) 2016;11(1):168–173. doi: 10.1515/med-2016-0032. - DOI - PMC - PubMed
    1. Prabhu VC, Melian E, Germanwala AV, Solanki AA, Borys E, Barton K, Anderson DE. Cranial base meningiomas. World Neurosurg. 2018;109:258–262. doi: 10.1016/j.wneu.2017.09.207. - DOI - PubMed

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