Next Article in Journal
Nordalbergin Synergizes with Novel β-Lactam Antibiotics against MRSA Infection
Previous Article in Journal
Comprehensive Analysis of Placental DNA Methylation Changes and Fetal Birth Weight in Pigs
Previous Article in Special Issue
Conventional Cytogenetic Analysis and Array CGH + SNP Identify Essential Thrombocythemia and Prefibrotic Primary Myelofibrosis Patients Who Are at Risk for Disease Progression
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the Gata1low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination

1
Department of Veterinary Medical Sciences, Alma Mater Studiorum University, 40126 Bologna, Italy
2
National Center for Drug Research and Evaluation, Istituto Superiore di Sanità, 00161 Rome, Italy
3
Department of Medical and Surgical Sciences, Alma Mater Studiorum University, 40126 Bologna, Italy
4
Altius Institute for Biomedical Sciences, Seattle, WA 98121, USA
5
Institute of Nanotechnology, National Research Council (Cnr-NANOTEC), c/o Campus Ecotekne, 73100 Lecce, Italy
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2024, 25(14), 7703; https://doi.org/10.3390/ijms25147703
Submission received: 9 May 2024 / Revised: 25 June 2024 / Accepted: 3 July 2024 / Published: 13 July 2024
(This article belongs to the Special Issue Molecular Research on Myeloproliferative Disorders)

Abstract

Studies conducted on animal models have identified several therapeutic targets for myelofibrosis, the most severe of the myeloproliferative neoplasms. Unfortunately, many of the drugs which were effective in pre-clinical settings had modest efficacy when tested in the clinic. This discrepancy suggests that treatment for this disease requires combination therapies. To rationalize possible combinations, the efficacy in the Gata1low model of drugs currently used for these patients (the JAK1/2 inhibitor Ruxolitinib) was compared with that of drugs targeting other abnormalities, such as p27kip1 (Aplidin), TGF-β (SB431542, inhibiting ALK5 downstream to transforming growth factor beta (TGF-β) signaling and TGF-β trap AVID200), P-selectin (RB40.34), and CXCL1 (Reparixin, inhibiting the CXCL1 receptors CXCR1/2). The comparison was carried out by expressing the endpoints, which had either already been published or had been retrospectively obtained for this study, as the fold change of the values in the corresponding vehicles. In this model, only Ruxolitinib was found to decrease spleen size, only Aplidin and SB431542/AVID200 increased platelet counts, and with the exception of AVID200, all the inhibitors reduced fibrosis and microvessel density. The greatest effects were exerted by Reparixin, which also reduced TGF-β content. None of the drugs reduced osteopetrosis. These results suggest that future therapies for myelofibrosis should consider combining JAK1/2 inhibitors with drugs targeting hematopoietic stem cells (p27Kip1) or the pro-inflammatory milieu (TGF-β or CXCL1).
Keywords: myelofibrosis; megakaryocytes; Gata1; TGF-β; P-selectin; IL-8 myelofibrosis; megakaryocytes; Gata1; TGF-β; P-selectin; IL-8

Share and Cite

MDPI and ACS Style

Gobbo, F.; Martelli, F.; Di Virgilio, A.; Demaria, E.; Sarli, G.; Migliaccio, A.R. The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the Gata1low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination. Int. J. Mol. Sci. 2024, 25, 7703. https://doi.org/10.3390/ijms25147703

AMA Style

Gobbo F, Martelli F, Di Virgilio A, Demaria E, Sarli G, Migliaccio AR. The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the Gata1low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination. International Journal of Molecular Sciences. 2024; 25(14):7703. https://doi.org/10.3390/ijms25147703

Chicago/Turabian Style

Gobbo, Francesca, Fabrizio Martelli, Antonio Di Virgilio, Elena Demaria, Giuseppe Sarli, and Anna Rita Migliaccio. 2024. "The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the Gata1low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination" International Journal of Molecular Sciences 25, no. 14: 7703. https://doi.org/10.3390/ijms25147703

APA Style

Gobbo, F., Martelli, F., Di Virgilio, A., Demaria, E., Sarli, G., & Migliaccio, A. R. (2024). The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the Gata1low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination. International Journal of Molecular Sciences, 25(14), 7703. https://doi.org/10.3390/ijms25147703

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop