Department of Pathology, University Hospital of Koeln, 50931, Koeln, Germany.
Biol Cell. 2019 Jul;111(7):169-186. doi: 10.1111/boc.201800059. Epub 2019 Apr 8.
This review highlights new developments in miRNA as diagnostic and surveillance tools in diseases damaging the renal proximal tubule mediated by endothelin in the field of renal carcinoma, proteinuric kidney disease and tubulotoxicity. A new mechanism in the miRNA regulation of proteins leads to the binding of the miRNA directly to the DNA with premature transcriptional termination and hence the formation of truncated protein isoforms (Mxi2, Vim3). These isoforms are mediated through miRNA15a or miRNA 498, respectively. ET-1 can activate a cytoplasmic complex consisting of NF-κB p65, MAPK p38α, and PKCα. Consequently, PKCα does not transmigrate into the nucleus, which leads to the loss of suppression of a primiRNA15a, maturation of this miRNA in the cytoplasm, tubular secretion and detectability in the urine. This mechanism has been shown in renal cell carcinoma and in proteinuric disease as a biomarker for the activation of the signalling pathway. Similarly, ET-1 induced miRNA 498 transmigrates into the nucleus to form the truncated protein Vim3, which is a biomarker for the benign renal cell tumour, oncocytoma. In tubulotoxicity, ET-1 induced miRNa133a down-regulating multiple-drug-resistant related protein-2, relevant for proteinuric and cisplatin/cyclosporine A toxicity. Current advantages and limitations of miRNAs as urinary biomarkers are discussed.
本文综述了 miRNA 在肾细胞癌、蛋白尿性肾病和肾小管毒性等领域中作为内皮素介导的肾近端小管损伤疾病的诊断和监测工具的新进展。miRNA 对蛋白质的调控的一个新机制导致 miRNA 直接与 DNA 结合,从而导致转录提前终止,并形成截短的蛋白异构体(Mxi2、Vim3)。这些异构体分别通过 miRNA15a 或 miRNA498 介导。ET-1 可以激活由 NF-κB p65、MAPK p38α 和 PKCα 组成的细胞质复合物。因此,PKCα 不会穿越到细胞核,从而导致抑制 primiRNA15a 的丧失,这种 miRNA 在细胞质中的成熟,以及在尿液中的分泌和可检测性。这一机制已在肾细胞癌和蛋白尿性疾病中被证明是信号通路激活的生物标志物。同样,ET-1 诱导的 miRNA498 穿越到细胞核形成截短蛋白 Vim3,这是良性肾细胞瘤、嗜酸细胞瘤的生物标志物。在肾小管毒性中,ET-1 诱导的 miRNa133a 下调多药耐药相关蛋白 2,与蛋白尿和顺铂/环孢素 A 毒性有关。本文讨论了 miRNA 作为尿生物标志物的当前优势和局限性。