Sheng Lili, Bayliss George, Zhuang Shougang
Department of Nephrology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Department of Medicine, Rhode Island Hospital and Alpert Medical School, Brown University, Providence, RI, United States.
Front Pharmacol. 2021 Jan 26;11:598910. doi: 10.3389/fphar.2020.598910. eCollection 2020.
Diabetic kidney disease (DKD) is a leading cause of end-stage renal disease worldwide and the major cause of renal failure among patients on hemodialysis. Numerous studies have demonstrated that transient activation of epidermal growth factor receptor (EGFR) pathway is required for promoting kidney recovery from acute injury whereas its persistent activation is involved in the progression of various chronic kidney diseases including DKD. EGFR-mediated pathogenesis of DKD is involved in hemodynamic alteration, metabolic disturbance, inflammatory response and parenchymal cellular dysfunction. Therapeutic intervention of this receptor has been available in the oncology setting. Targeting EGFR might also hold a therapeutic potential for DKD. Here we review the functional role of EGFR in the development of DKD, mechanisms involved and the perspective about use of EGFR inhibitors as a treatment for DKD.
糖尿病肾病(DKD)是全球终末期肾病的主要原因,也是血液透析患者肾衰竭的主要原因。大量研究表明,表皮生长因子受体(EGFR)通路的短暂激活是促进肾脏从急性损伤中恢复所必需的,而其持续激活则与包括DKD在内的各种慢性肾病的进展有关。EGFR介导的DKD发病机制涉及血流动力学改变、代谢紊乱、炎症反应和实质细胞功能障碍。这种受体的治疗干预已应用于肿瘤学领域。靶向EGFR可能对DKD也具有治疗潜力。在此,我们综述EGFR在DKD发生发展中的功能作用、相关机制以及使用EGFR抑制剂治疗DKD的前景。