Roth Katherine J, Copple Bryan L
Department of Pharmacology and Toxicology, the Institute for Environmental Toxicology, and the Program in Cellular and Molecular Biology, Michigan State University, East Lansing, Michigan.
Cell Mol Gastroenterol Hepatol. 2015 Sep 25;1(6):589-597. doi: 10.1016/j.jcmgh.2015.09.005. eCollection 2015 Nov.
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.
在美国乃至全世界,肝纤维化仍然是一个重大的临床问题。尽管在对这种疾病的认识上已经取得了重要进展,但尚未开发出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案例都针对纤维化的病因进行治疗,例如开发根除肝炎病毒的新型抗病毒药物。然而,对于许多患者来说,这并不可行,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点,以减缓或逆转此类患者的纤维化进程。过去16年的研究已将缺氧诱导因子(HIFs)确定为驱动肝纤维化诸多方面的关键转录因子,使其成为潜在的治疗靶点。在这篇综述中,我们讨论了关于HIFs与肝纤维化的最新研究成果,包括这些转录因子在肝纤维化发展过程中的细胞特异性功能。