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Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
PLK1-associated microRNAs are correlated with pediatric medulloblastoma prognosis
Julia Alejandra Pezuk1,2, María Sol Brassesco3, Ricardo Santos de Oliveira4
1Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil. julia.pezuk@hotmail.com.
Purpose:
Medulloblastoma (MB) is the most common malignant tumor of the central nervous system (CNS) in children. Despite its relative good survival rates, treatment can cause long time sequels and may impair patients' lifespan and quality, making the search for new treatment options still necessary. Polo like kinases (PLKs) constitute a five-member serine/threonine kinases family (PLK 1-5) that regulates different stages during cell cycle. Abnormal PLKs expression has been observed in several cancer types, including MB. As gene regulators, miRNAs have also been described with variable expression in cancer.
Methods:
We evaluated gene expression profiles of all PLK family members and related miRNAs (miR-100, miR-126, miR-219, and miR-593*) in MB cell lines and tumor samples.
Results:
RT-qPCR analysis revealed increased levels of PLK1-4 in all cell lines and in most MB samples, while PLK5 was found underexpressed. In parallel, miR-100 was also found upregulated while miR-129, miR-216, and miR-593* were decreased in MB cell lines. Variable miRNAs expression patterns were observed in MB samples. However, a correlation between miR-100 and PLK4 expression was observed, and associations between miR-100, miR-126, and miR-219 expression and overall and event free survival were also evinced in our cohort. Moreover, despite the lack of association with clinico-pathological features, when comparing primary tumors to those relapsed, we found a consistent decrease on PLK2, miR-219, and miR-598* and an increase on miR-100 and miR-126.
Conclusion:
Specific dysregulation on PLKs and associated miRNAs may be important in MB and can be used to predict prognosis. Although miRNAs sequences are fundamental to predict its target, the cell type may also be consider once that mRNA repertoire can define different roles for specific miRNA in a given cell.
Insights
Specific Polo-like Kinases (PLKs) and microRNAs (miRNAs) are dysregulated in medulloblastoma (MB), a pediatric brain tumor. Their altered expression may serve as a prognostic marker for MB patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Medulloblastoma (MB) is a common pediatric central nervous system (CNS) malignancy.
- Current treatments for MB can lead to long-term adverse effects, necessitating novel therapeutic strategies.
- Polo-like kinases (PLKs) and microRNAs (miRNAs) are implicated in various cancers, including MB.
Purpose of the Study:
- To investigate the expression profiles of Polo-like Kinase (PLK) family members and associated microRNAs (miRNAs) in medulloblastoma (MB).
- To explore the potential of these molecules as prognostic biomarkers for MB.
Main Methods:
- Gene expression profiling of PLK family members (PLK1-5) and specific miRNAs (miR-100, miR-126, miR-219, miR-593*) in MB cell lines and tumor samples.
- Quantitative real-time PCR (RT-qPCR) was employed for expression analysis.
Main Results:
- PLK1-4 were upregulated, while PLK5 was downregulated in MB cell lines and samples.
- miR-100 was upregulated, whereas miR-129, miR-216, and miR-593* were downregulated in MB cell lines.
- Correlations were observed between miR-100 and PLK4 expression, and associations between specific miRNAs and patient survival (overall and event-free).
- Relapsed tumors showed distinct expression patterns for PLK2, miR-219, miR-593*, miR-100, and miR-126 compared to primary tumors.
Conclusions:
- Dysregulation of PLKs and associated miRNAs plays a significant role in medulloblastoma (MB) pathogenesis.
- These molecular alterations hold potential as predictive biomarkers for MB prognosis.
- Cell type-specific mRNA repertoire influences miRNA function, highlighting the complexity of miRNA-mediated gene regulation in MB.
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