Authors
A Barry, S. F. Samuel, I. Hosni, A. Moursi, L. Feugere, C. Sennett, S. Deepak, S. Achawal, C. Rajaraman, A. Iles, K. C. Wollenberg Valero, I. S. Scott, V. L. Green, L. F. Stead, J. Greenman, M. A. Wade, P. Beltran-Alvarez
Publication date
2023/5
Journal
Lab on a Chip
Pages
DOI: 10.1039/D3LC00204G
Publisher
Royal Society of Chemistry
Description
Arginine methylation is a post-translational modification that consists of the transfer of one or two methyl (CH3) groups to arginine residues in proteins. Several types of arginine methylation occur, namely monomethylation, symmetric dimethylation and asymmetric dimethylation, which are catalysed by different protein arginine methyltransferases (PRMTs). Inhibitors of PRMTs have recently entered clinical trials to target several types of cancer, including gliomas (NCT04089449). People with glioblastoma (GBM), the most aggressive form of brain tumour, are among those with the poorest quality of life and likelihood of survival of anyone diagnosed with cancer. There is currently a lack of (pre)clinical research on the possible application of PRMT inhibitors to target brain tumours. Here, we set out to investigate the effects of clinically-relevant PRMT inhibitors on GBM biopsies. We present a new, low-cost, easy to …
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