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MicroRNA-18a regulates invasive meningiomas via hypoxia-inducible factor-1α
Puxian Li1, Yong Gao1, Fengjia Li1
1Department of Neurosurgery, Laiwu City People's Hospital, Laiwu, Shandong 271100, P.R. China.
Abstract:
The aim of the present study was to investigate the effects of microRNA-18a (miR-18a) on the invasiveness and metastasis of invasive meningiomas and the underlying mechanism. A total of 69 patients with meningiomas (30 patients in the invasive meningioma group and 39 patients in the non-invasive meningioma group) and 48 cases in the control group were enrolled. Samples of meningioma tissues, serum and cerebrospinal fluid were collected. Reverse transcription-quantitative polymerase chain reaction was performed to quantify the expression levels of hypoxia-inducible factor-1α (HIF-1α) mRNA and miR-18a. Western blot analysis was used to determine protein expression levels of HIF-1α. The expression levels of HIF-1α mRNA and protein in all three types of sample from the invasive meningioma group were significantly higher compared with those in the control and non-invasive meningioma groups (P<0.05), and the expression levels of HIF-1α mRNA in the serum and cerebrospinal fluid of the non-invasive meningioma group were significantly higher compared with those in the control group (P<0.05). The expression levels of miR-18a in the invasive meningioma group were significantly reduced compared with those in the control and non-invasive meningioma groups (P<0.05), whereas the levels of miR-18a in the non-invasive meningioma group were significantly lower compared with those in the control group (P<0.05). The expression of HIF-1α is significantly upregulated in patients with invasive meningiomas, possibly due to the downregulation of miR-18a expression. Therefore, miR-18a may regulate invasive meningiomas via HIF-1α.
Insights
MicroRNA-18a (miR-18a) is downregulated in invasive meningiomas, leading to increased hypoxia-inducible factor-1α (HIF-1α) expression. This suggests miR-18a may inhibit meningioma invasion and metastasis by regulating HIF-1α.
Area of Science:
- Neuro-oncology
- Molecular Biology
- Biochemistry
Background:
- Meningiomas are primary tumors of the central nervous system, with invasive subtypes posing significant clinical challenges.
- Understanding the molecular mechanisms driving meningioma invasiveness and metastasis is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the role of microRNA-18a (miR-18a) in the invasiveness and metastasis of invasive meningiomas.
- To elucidate the underlying molecular mechanism involving hypoxia-inducible factor-1α (HIF-1α).
Main Methods:
- Quantitative analysis of miR-18a and HIF-1α mRNA expression using reverse transcription-quantitative polymerase chain reaction (RT-qPCR).
- Protein expression levels of HIF-1α were determined by Western blot analysis.
- Samples included meningioma tissues, serum, and cerebrospinal fluid from patients and controls.
Main Results:
- Hypoxia-inducible factor-1α (HIF-1α) mRNA and protein levels were significantly elevated in invasive meningioma tissues, serum, and cerebrospinal fluid compared to controls.
- MicroRNA-18a (miR-18a) expression was significantly reduced in invasive meningiomas compared to non-invasive and control groups.
- A negative correlation was observed between miR-18a expression and HIF-1α levels, suggesting miR-18a downregulates HIF-1α.
Conclusions:
- Hypoxia-inducible factor-1α (HIF-1α) is upregulated in invasive meningiomas, potentially driven by the downregulation of microRNA-18a (miR-18a).
- MicroRNA-18a (miR-18a) may function as a tumor suppressor by inhibiting meningioma invasiveness and metastasis through the regulation of HIF-1α.
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