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Advanced molecular characterization using Digital Spatial Profiling Technology on immuno-oncology targets in methylated compared with unmethylated IDH-wildtype glioblastoma

Ren, X.; Barber, H.; Tofias, A.; Lander, B.; Daniels, A.; Gong, J.; Ren, Y.; Liang, Y.; White, P.; Kurian, K. M.

Advanced molecular characterization using Digital Spatial Profiling Technology on immuno-oncology targets in methylated compared with unmethylated IDH-wildtype glioblastoma Thumbnail


Authors

X. Ren

H. Barber

A. Tofias

B. Lander

A. Daniels

J. Gong

Y. Ren

Y. Liang

Paul White Paul.White@uwe.ac.uk
Professor in Applied Statistics

K. M. Kurian



Abstract

Introduction. Glioblastoma (GBM) is the most common primary adult brain tumour with a median overall survival (OS) of 12-15 months. Molecular characterization of multiple immunooncology targets in GBM may help target novel immunotherapeutic strategies. We used NanoString GeoMx® Digital Spatial Profiling (DSP) to assess multiple immunooncology protein targets in methylated versus unmethylated IDH-wild-type glioblastoma. Methods. NanoString GeoMx® DSP technology uses multiple primary antibodies conjugated to indexing DNA oligos with a UV photocleavable linker. Tissue regions of interest (ROIs) are selected with bound fluorescent antibodies; oligos are released via a UV-mediated linker and quantitated. We used DSP multiplex analysis of 31 immunooncology proteins and controls (CD4, CD14, CD68, CD8A, B7-H3, PD-L1, CD19, FOXP3, CD44, STAT3 (phospho Y705), CD45, Pan Cytokeratin, MS4A1/CD20, CD45RO, PD1, CD3, beta-2 microglobulin, VISTA, Bcl2, GZMB, PTEN, beta-catenin, CD56, Ki-67, STAT3, AKT, p-Akt, S6, Histone H3, IgG Rabbit control, and Mouse IgG control) from ROIs in a cohort of 10 IDH-wild-type glioblastomas (5 methylated and 5 unmethylated). An nCounter platform allowed quantitative comparisons of antibodies between ROIs in MGMT methylated and unmethylated tumours. Mean protein expression counts between methylated and unmethylated GBM were compared using technical and biological replicates. Results. The analysis showed 10/27 immunooncology target proteins were significantly increased in methylated versus unmethylated IDH-wild-type glioblastoma tumour core (false discovery rate (FDR)

Citation

Ren, X., Barber, H., Tofias, A., Lander, B., Daniels, A., Gong, J., …Kurian, K. M. (2021). Advanced molecular characterization using Digital Spatial Profiling Technology on immuno-oncology targets in methylated compared with unmethylated IDH-wildtype glioblastoma. Journal of Oncology, 2021, Article 8819702. https://doi.org/10.1155/2021/8819702

Journal Article Type Article
Acceptance Date Feb 2, 2021
Online Publication Date Feb 24, 2021
Publication Date Feb 24, 2021
Deposit Date Feb 2, 2021
Publicly Available Date Apr 15, 2021
Journal Journal of Oncology
Print ISSN 1687-8450
Electronic ISSN 1687-8469
Publisher Hindawi
Peer Reviewed Peer Reviewed
Volume 2021
Article Number 8819702
DOI https://doi.org/10.1155/2021/8819702
Public URL https://uwe-repository.worktribe.com/output/7046885

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