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Dysregulation of the MMP/TIMP Proteolytic System in Subependymal Giant Cell Astrocytomas in Patients With Tuberous Sclerosis Complex: Modulation of MMP by MicroRNA-320d In Vitro

Bongaarts, A., de Jong, J. M., Broekaart, D. W. M., van Scheppingen, J., Anink, J. J., Mijnsbergen, C., Jansen, F. E., Spliet, W. G. M., den Dunnen, W. F. A., Gruber, V. E., Scholl, T., Hainfellner, J. A., Feucht, M., Borkowska, J., Kotulska, K., Jozwiak, S., Grajkowska, W., Buccoliero, A. M., Caporalini, C., Giordano, F., Genitori, L., Scicluna, B. P., Schouten-van Meeteren, A. Y. N., van Vliet, E. A., Mühlebner, A., Mills, J. D. & Aronica, E., Jul-2020, In : Journal of neuropathology and experimental neurology. 79, 7, p. 777-790 14 p., nlaa040.

Research output: Contribution to journalArticleAcademicpeer-review

  • Anika Bongaarts
  • Jody M de Jong
  • Diede W M Broekaart
  • Jackelien van Scheppingen
  • Jasper J Anink
  • Caroline Mijnsbergen
  • Floor E Jansen
  • Wim G M Spliet
  • Wilfred F A den Dunnen
  • Victoria E Gruber
  • Theresa Scholl
  • Johannes A Hainfellner
  • Martha Feucht
  • Julita Borkowska
  • Katarzyna Kotulska
  • Sergiusz Jozwiak
  • Wieslawa Grajkowska
  • Anna Maria Buccoliero
  • Chiara Caporalini
  • Flavio Giordano
  • Lorenzo Genitori
  • Brendon P Scicluna
  • Antoinette Y N Schouten-van Meeteren
  • Erwin A van Vliet
  • Angelika Mühlebner
  • James D Mills
  • Eleonora Aronica

Tuberous sclerosis complex (TSC), a rare genetic disorder caused by a mutation in the TSC1 or TSC2 gene, is characterized by the growth of hamartomas in several organs. This includes the growth of low-grade brain tumors, known as subependymal giant cell astrocytomas (SEGA). Previous studies have shown differential expression of genes related to the extracellular matrix in SEGA. Matrix metalloproteinases (MMPs), and their tissue inhibitors (TIMPs) are responsible for remodeling the extracellular matrix and are associated with tumorigenesis. This study aimed to investigate the MMP/TIMP proteolytic system in SEGA and the regulation of MMPs by microRNAs, which are important post-transcriptional regulators of gene expression. We investigated the expression of MMPs and TIMPs using previously produced RNA-Sequencing data, real-time quantitative PCR and immunohistochemistry in TSC-SEGA samples and controls. We found altered expression of several MMPs and TIMPs in SEGA compared to controls. We identified the lowly expressed miR-320d in SEGA as a potential regulator of MMPs, which can decrease MMP2 expression in human fetal astrocyte cultures. This study provides evidence of a dysregulated MMP/TIMP proteolytic system in SEGA of which MMP2 could be rescued by microRNA-320d. Therefore, further elucidating microRNA-mediated MMP regulation may provide insights into SEGA pathogenesis and identify novel therapeutic targets.

Original languageEnglish
Article numbernlaa040
Pages (from-to)777-790
Number of pages14
JournalJournal of neuropathology and experimental neurology
Volume79
Issue number7
Publication statusPublished - Jul-2020

    Keywords

  • Extracellular matrix, Matrix metalloproteinases, MicroRNA, Subependymal giant cell astrocytoma (SEGA), Tuberous sclerosis complex, CENTRAL-NERVOUS-SYSTEM, MATRIX METALLOPROTEINASES, CORTICAL TUBERS, GENE-EXPRESSION, TUMORS, BRAIN, ACTIVATION, MIGRATION, TSC1, MATRIX-METALLOPROTEINASE-9

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