放射性纤维化的治疗方法。

Edward J Macarak, Joel Rosenbloom
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引用次数: 1

摘要

放射诱导纤维化(RIF)是接受放射治疗的癌症患者的常见疾病。脱靶效应导致强烈的炎症反应,最终导致细胞外基质(ECM)的产生,产生肌成纤维细胞,介导进行性纤维化,导致疤痕和器官和组织功能障碍。不幸的是,目前还没有有效的治疗方法来阻止ECM的过度积累。我们之前报道过使用曲美替尼(一种MEK抑制剂)在盲肠磨损小鼠模型中基本上阻断腹腔粘连的形成。在小鼠模型中使用该药物可阻断前体细胞向产生ecm的肌成纤维细胞的完全反分化。曲美替尼是一种潜在的强大药物,可以阻止RIF中的器官和组织纤维化,因为它具有潜在的双重功能,既可以阻断RIF,又可以防止辐射抗性。考虑到RIF的难治性,曲美替尼应考虑进行更广泛的试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Approaches to Radiation-Induced Fibrosis.

Radiation induced fibrosis (RIF) is a common morbidity in patients being treated for cancer with radiation. Off-target effects result in intense inflammatory responses which ultimately results in the generation of extracellular matrix (ECM) producing myofibroblasts which mediate a progressive fibrosis resulting in scarring and organ and tissue dysfunction. Unfortunately, currently, there are no effective therapies to block the excess accumulation of ECM. We have previously reported on the use of trametinib, a MEK inhibitor, to essentially block the formation of abdominal adhesions in a mouse model of cecal abrasion. Using this drug in the mouse model, the complete trans-differentiation of precursor cells into ECM-producing myofibroblasts was blocked. Trametinib is a potentially powerful drug to thwart organ and tissue fibrosis in RIF because it has a potential dual function in that it may block RIF as well as prevent radiation-resistance. Given the intractability of RIF, trametinib should be considered for more extensive testing.

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