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.

Abstract

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.

Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
4.2K
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
24.4K
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.3K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
5.0K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
6.0K