Cited by 32MicroRNA in disease regulationGlioma Diagnosis and TreatmentCancer-related molecular mechanisms research

Analysis of expression of microRNAs and genes involved in the control of key signaling mechanisms that support or inhibit development of brain tumors of different grades

Koshkin, Philip Alexandrovich, Chistiakov, Dimitry Alexandrovich, Nikitin, Alexey Georgievich, Konovalov, Alexander Nikolaevich, Potapov, Alexander Alexandrovich, Usachev, Dmitry Yrevich, Pitskhelauri, David Ilich, Kobyakov, Gregory Lvovich +2 more·2014·Clinica Chimica Acta

Abstract

Background MicroRNAs (miRNAs) are a class of small non-coding RNA molecules involved in the regulation of key biological processes. Different miRNAs with pro-oncogenic and anti-oncogenic properties have been identified in glioblastomas. We decided to analyze expression profiles of 10 mature miRNAs (miR-7-1, miR-10а, miR-17, miR-20а, miR-21, miR-23а, miR-26а, miR-137, and miR-222) in post-surgery glioma specimens of different grades in order to find whether the expression level correlates with tumor grades. We also measured expression of six key genes such as PTEN, p21/CDKN1A, MDR1, ABCG2, BAX, and BCL-2 involved in the regulation of critical glioma signaling pathways to establish the effect of miRNAs on these signaling mechanisms. Methods Using RT-PCR, we performed expression analysis of 25 tumor fresh samples (grades II-IV). Results We found gradual increase in miR-21 and miR-23a levels in all tumor grades whereas miR-7 and miR-137 were significantly down-regulated depending on the glioma grade. MDR, ABCG2, and p21/CDKN1A levels were significantly up-regulated while expression of PTEN was down-regulated in tumor samples compared to the normal brain tissue. Conclusions These observations provide new insights into molecular pathogenic mechanisms of glioma progression and suggest about a potential value of miRNAs as a putative diagnostic marker of brain tumors.

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Crossref · 10.1016/j.cca.2014.01.001

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  • Expression changes of miR-23a are related to angiogenesis of glioblastoma microvascular proliferation tissue.

    “the expression changes of miR-23a are related to the angiogenesis of glioblastoma microvascular proliferation tissue.”
  • miR-23a expression level is elevated in postoperative glioma specimens of various grades, and this elevation is associated with downregulation of PTEN expression.

    “the expression level of miR-23a is elevated in postoperative glioma specimens of various grades, and this elevation is associated with the downregulation of PTEN expression”
  • In glioblastoma microvascular proliferation tissue, miR-23 is downregulated, while its target genes ATP5A1 and ATP5B are highly expressed in endothelial cells.

    “In this context, miR-23 is downregulated, while its target genes ATP5A1 and ATP5B are highly expressed in endothelial cells.”

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Authors
Koshkin, P. A., Chistiakov, D. A., Nikitin, A. G., Konovalov, A. N., Potapov, A. A., Usachev, D. Y., Pitskhelauri, D. I., Kobyakov, G. L., Shishkina, L. V., & Chekhonin, V. P.
Affiliations
  • Pirogov Russian National Research Medical University (RU)
  • Burdenko Neurosurgery Institute (RU)
Corresponding author
  • Koshkin, Philip Alexandrovich
  • Chistiakov, Dimitry Alexandrovich
Venue
Clinica Chimica Acta
Publisher
Elsevier BV
Published
2014-03
Volume
430
Pages
55-62
ISSN
0009-8981 (ISSN-L)
OpenAlex
W2027497735
Cited by
32
References
2
Citations by year
2024: 3 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 7 · 2018: 5 · 2017: 3 · 2016: 2 · 2015: 3 · 2014: 4
FWCI
1.28
Type
journal article
Language
en
Open access
closed
Locations
  • Clinica Chimica Acta (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
Keywords
microRNA, glioma, glioblastoma, tumor grade, miR-21, miR-23a, miR-7, miR-137, PTEN, CDKN1A/p21, MDR1, ABCG2, Bax, Bcl-2, tumor progression, diagnostic biomarkers
MeSH terms
Adult, Aged, Brain Neoplasms, Female, Humans, Male, Middle Aged, Signal Transduction, Gene Expression Regulation, Neoplastic, Gene Expression Profiling, MicroRNAs, Young Adult, Neoplasm Grading

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