PUBLICATION

TRIM28 Selective Nanobody Reduces Glioblastoma Stem Cell Invasion

Authors
Porčnik, A., Novak, M., Breznik, B., Majc, B., Hrastar, B., Šamec, N., Zottel, A., Jovčevska, I., Vittori, M., Rotter, A., Komel, R., Lah Turnšek, T.
ID
ZDB-PUB-210911-2
Date
2021
Source
Molecules   26(17): (Journal)
Registered Authors
Keywords
TRIM28, cell invasion, glioblastoma, glioblastoma stem cells, nanobody, transcription factor
MeSH Terms
  • Animals
  • Brain/metabolism
  • Brain/pathology
  • Brain Neoplasms/metabolism*
  • Brain Neoplasms/pathology
  • Cell Line, Tumor
  • Glioblastoma/metabolism*
  • Glioblastoma/pathology
  • Humans
  • Neoplastic Stem Cells/metabolism
  • Neoplastic Stem Cells/pathology
  • Prognosis
  • Tripartite Motif-Containing Protein 28/metabolism*
  • Zebrafish/metabolism
PubMed
34500575 Full text @ Molecules
Abstract
Glioblastoma (GB), is the most common and aggressive malignant primary brain tumour in adults. Intra- and inter-tumour heterogeneity, infiltrative GB cell invasion and presence of therapy-resistant GB stem cells (GSCs) represent major obstacles to favourable prognosis and poor therapy response. Identifying the biomarkers of the most aggressive tumour cells and their more efficient targeting strategies are; therefore, crucial. Recently, transcription factor TRIM28 has been identified as a GB biomarker and, in this study, we have shown high expression of TRIM28 in GB and in low grade gliomas as well as higher expression in GSCs vs. differentiated GB cells, although in both cases not significant. We demonstrated significant in vitro inhibition of GB cells and GSCs invasiveness and spread in zebrafish brains in vivo by anti-TRIM28 selective nanobody NB237. TRIM28 was also enriched in GB (tumour) core and associated with the expression of stem cell genes, but was not prognostic for overall survival. However, based on the above results, we conclude that TRIM28 nanobody NB237 offers a new opportunity as a GB therapeutic tool.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping