Protein Arginine Methyltransferases as Therapeutic Targets in Hematological Malignancies

• Published in: Cancers Vol. 14; no. 21; p. 5443
• Main Authors: Sauter, Camille, Simonet, John, Guidez, Fabien, Dumétier, Baptiste, Pernon, Baptiste, Callanan, Mary, Bastie, Jean-Noël, Aucagne, Romain, Delva, Laurent
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2022; MDPI
• Subjects: Animal models; Antigens; Apoptosis; Arginine; Blood cells; Cancer; Care and treatment; Cell activation; Cell culture; Cell cycle; Cell differentiation; Cell viability; Clinical trials; Cyclin-dependent kinases; DNA damage; DNA methylation; DNA repair; Drug targeting; Enzymatic activity; Enzymes; Epigenetics; Health aspects; Hematology; Hemopoiesis; Histones; Immunodeficiency; Kinases; Lymphoma; Malignancy; Medical prognosis; Methods; Methyltransferases; Post-translation; Progenitor cells; Proteins; Review; Roles; Stem cells; Therapeutic targets; Transcription; Xenografts; France
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers14215443

Arginine methylation is a common post-translational modification affecting protein activity and the transcription of target genes when methylation occurs on histone tails. There are nine protein arginine methyltransferases (PRMTs) in mammals, divided into subgroups depending on the methylation they form on a molecule of arginine. During the formation and maturation of the different types of blood cells, PRMTs play a central role by controlling cell differentiation at the transcriptional level. PRMT enzymatic activity is necessary for many cellular processes in hematological malignancies, such as the activation of cell cycle and proliferation, inhibition of apoptosis, DNA repair processes, RNA splicing, and transcription by methylating histone tails’ arginine. Chemical tools have been developed to inhibit the activity of PRMTs and have been tested in several models of hematological malignancies, including primary samples from patients, xenografts into immunodeficient mice, mouse models, and human cell lines. They show a significant effect by reducing cell viability and increasing the overall survival of mice. PRMT5 inhibitors have a strong therapeutic potential, as phase I clinical trials in hematological malignancies that use these molecules show promising results, thus, underlining PRMT inhibitors as useful therapeutic tools for cancer treatment in the future.