دورية أكاديمية
In Humanized Sickle Cell Mice, Imatinib Protects Against Sickle Cell–Related Injury
العنوان: | In Humanized Sickle Cell Mice, Imatinib Protects Against Sickle Cell–Related Injury |
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المؤلفون: | Enrica Federti, Alessandro Matte, Antonio Recchiuti, Francesca Garello, Alessandra Ghigo, Wassim El Nemer, Enzo Terreno, Angela Amoresano, Domenico Mattoscio, Franco Turrini, Christophe Lebouef, Anne Janin, Antonella Pantaleo, Roberta Russo, Mickael Marin, Iana Iatcencko, Veronica Riccardi, Angela Siciliano, Achille Iolascon, Carlo Brugnara, Lucia De Franceschi |
المصدر: | HemaSphere, Vol 7, Iss 3, p e848 (2023) |
بيانات النشر: | Wiley, 2023. |
سنة النشر: | 2023 |
المجموعة: | LCC:Diseases of the blood and blood-forming organs |
مصطلحات موضوعية: | Diseases of the blood and blood-forming organs, RC633-647.5 |
الوصف: | Drug repurposing is a valuable strategy for rare diseases. Sickle cell disease (SCD) is a rare hereditary hemolytic anemia accompanied by acute and chronic painful episodes, most often in the context of vaso-occlusive crisis (VOC). Although progress in the knowledge of pathophysiology of SCD have allowed the development of new therapeutic options, a large fraction of patients still exhibits unmet therapeutic needs, with persistence of VOCs and chronic disease progression. Here, we show that imatinib, an oral tyrosine kinase inhibitor developed for the treatment of chronic myelogenous leukemia, acts as multimodal therapy targeting signal transduction pathways involved in the pathogenesis of both anemia and inflammatory vasculopathy of humanized murine model for SCD. In addition, imatinib inhibits the platelet-derived growth factor-B–dependent pathway, interfering with the profibrotic response to hypoxia/reperfusion injury, used to mimic acute VOCs. Our data indicate that imatinib might be considered as possible new therapeutic tool for chronic treatment of SCD. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2572-9241 00000000 |
العلاقة: | http://journals.lww.com/10.1097/HS9.0000000000000848Test; https://doaj.org/toc/2572-9241Test |
DOI: | 10.1097/HS9.0000000000000848 |
الوصول الحر: | https://doaj.org/article/c8c05eebb53a44d484b867d2b88dc0d7Test |
رقم الانضمام: | edsdoj.8c05eebb53a44d484b867d2b88dc0d7 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 25729241 00000000 |
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DOI: | 10.1097/HS9.0000000000000848 |