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Role of Hypoxia-Inducible Factors in the Development of Liver Fibrosis

机译:缺氧诱导因子在肝纤维化发展中的作用

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摘要

Liver fibrosis remains a significant clinical problem in the United States and throughout the world. Although important advances in the understanding of this disease have been made, no effective pharmacologic agents have been developed that directly prevent or reverse the fibrotic process. Many of the successes in liver fibrosis treatment have been targeted toward treating the cause of fibrosis, such as the development of new antivirals that eradicate hepatitis virus. For many patients, however, this is not feasible, so a liver transplant remains the only viable option. Thus, there is a critical need to identify new therapeutic targets that will slow or reverse the progression of fibrosis in such patients. Research over the last 16 years has identified hypoxia-inducible factors (HIFs) as key transcription factors that drive many aspects of liver fibrosis, making them potential targets of therapy. In this review, we discuss the latest work on HIFs and liver fibrosis, including the cell-specific functions of these transcription factors in the development of liver fibrosis.
机译:在美国和全世界,肝纤维化仍然是一个重要的临床问题。尽管在了解这种疾病方面已取得重要进展,但尚未开发出可直接预防或逆转纤维化过程的有效药物。肝纤维化治疗的许多成功都针对治疗纤维化的原因,例如开发了可消灭肝炎病毒的新型抗病毒药。但是,对于许多患者而言,这是不可行的,因此肝移植仍然是唯一可行的选择。因此,迫切需要确定新的治疗靶标,这些靶标将减缓或逆转此类患者的纤维化进程。过去16年的研究已经将缺氧诱导因子(HIFs)作为驱动肝纤维化许多方面的关键转录因子,使其成为潜在的治疗靶标。在这篇综述中,我们讨论了有关HIF和肝纤维化的最新工作,包括这些转录因子在肝纤维化发展中的细胞特异性功能。

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