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本文引用的文献

1
Unique Transcriptional Programs Identify Subtypes of AKI.独特的转录程序可识别急性肾损伤的亚型。
J Am Soc Nephrol. 2017 Jun;28(6):1729-1740. doi: 10.1681/ASN.2016090974. Epub 2016 Dec 27.
2
KIM-1 Is a Potential Urinary Biomarker of Obstruction: Results from a Prospective Cohort Study.KIM-1是梗阻的潜在尿液生物标志物:一项前瞻性队列研究的结果。
J Endourol. 2017 Feb;31(2):111-118. doi: 10.1089/end.2016.0215. Epub 2016 Dec 19.
3
Whole-transcriptome analysis of UUO mouse model of renal fibrosis reveals new molecular players in kidney diseases.肾纤维化UUO小鼠模型的全转录组分析揭示了肾脏疾病中的新分子参与者。
Sci Rep. 2016 May 18;6:26235. doi: 10.1038/srep26235.
4
Keratins are novel markers of renal epithelial cell injury.角蛋白是肾上皮细胞损伤的新型标志物。
Kidney Int. 2016 Apr;89(4):792-808. doi: 10.1016/j.kint.2015.10.015. Epub 2016 Feb 6.
5
Proximal tubule proteins are significantly elevated in bladder urine of patients with ureteropelvic junction obstruction and may represent novel biomarkers: A pilot study.输尿管肾盂连接处梗阻患者膀胱尿液中的近端肾小管蛋白显著升高,可能代表新型生物标志物:一项初步研究。
J Pediatr Urol. 2016 Apr;12(2):120.e1-7. doi: 10.1016/j.jpurol.2015.10.008. Epub 2015 Nov 28.
6
Molecular Markers of Tubulointerstitial Fibrosis and Tubular Cell Damage in Patients with Chronic Kidney Disease.慢性肾脏病患者肾小管间质纤维化和肾小管细胞损伤的分子标志物
PLoS One. 2015 Aug 28;10(8):e0136994. doi: 10.1371/journal.pone.0136994. eCollection 2015.
7
Identification of a common molecular pathway in hypertensive renal damage: comparison of rat and human gene expression profiles.高血压性肾损害中常见分子途径的鉴定:大鼠和人类基因表达谱的比较
J Hypertens. 2015 Mar;33(3):584-96; discussion 596. doi: 10.1097/HJH.0000000000000395.
8
Gene expression analysis and urinary biomarker assays reveal activation of tubulointerstitial injury pathways in a rodent model of chronic proteinuria (Doxorubicin nephropathy).基因表达分析和尿生物标志物检测显示,在慢性蛋白尿(阿霉素肾病)的啮齿动物模型中,肾小管间质损伤途径被激活。
Nephron Exp Nephrol. 2013;124(1-2):1-10. doi: 10.1159/000355542. Epub 2013 Nov 12.
9
Molecular basis of renal adaptation in a murine model of congenital obstructive nephropathy.先天性梗阻性肾病小鼠模型中肾适应的分子基础。
PLoS One. 2013 Sep 4;8(9):e72762. doi: 10.1371/journal.pone.0072762. eCollection 2013.
10
Urinary NGAL levels correlate with differential renal function in patients with ureteropelvic junction obstruction undergoing pyeloplasty.尿中性粒细胞明胶酶相关脂质运载蛋白水平与肾盂成形术治疗肾盂输尿管连接部梗阻患者的肾功能差异相关。
J Urol. 2013 Oct;190(4 Suppl):1462-7. doi: 10.1016/j.juro.2013.05.003. Epub 2013 Jun 20.

鉴定与输尿管梗阻导致的肾损伤相关的转录本作为候选尿生物标志物。

Identification of transcripts associated with renal damage due to ureteral obstruction as candidate urinary biomarkers.

机构信息

Department of Urology, Stanford University , Stanford, California.

出版信息

Am J Physiol Renal Physiol. 2018 Jul 1;315(1):F16-F26. doi: 10.1152/ajprenal.00382.2017. Epub 2018 Feb 28.

DOI:10.1152/ajprenal.00382.2017
PMID:29488389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6087789/
Abstract

Renal obstruction is a common cause of renal failure in adults and children and is suspected when hydronephrosis is detected on imaging. Because not all cases of hydronephrosis are associated with renal damage, biomarkers are needed to guide intervention to relieve obstruction. We performed gene expression profiling on the kidneys from adult mice over a detailed time course after obstruction and compared these data with a neonatal model of bilateral high-grade obstruction induced by conditional deletion of the calcineurin β gene. Having identified a set of 143 transcripts modulated in both adult and neonatal obstruction, we tested their expression in a model of short-term obstruction (1 day), where renal damage is transient and reversible, and long-term obstruction (5 days), where significant renal damage is permanent. A significant number of transcripts increased early after obstruction, and later normalized, while 26 transcripts remained elevated 10 and 28 days after relief of 5 days of ureteral obstruction. With the use of qPCR, elevated levels of several of these candidate RNA biomarkers of renal damage were detected in urine from obstructed mice. In addition, several of these candidate RNA biomarkers of damage resulting from obstruction were detectable in catheterized urine samples from children undergoing surgery for ureteropelvic junction obstruction. Measurement of urinary transcripts modulated in response to renal obstruction could serve as biomarkers of renal damage with important clinical applications.

摘要

肾梗阻是成人和儿童肾衰竭的常见原因,当影像学检查发现肾积水时,就会怀疑存在肾梗阻。由于并非所有肾积水病例都与肾损伤有关,因此需要生物标志物来指导干预以解除梗阻。我们对梗阻后成年小鼠肾脏进行了详细时间过程的基因表达谱分析,并将这些数据与条件性删除钙调神经磷酸酶 β 基因诱导的双侧高级别梗阻的新生儿模型进行了比较。在成年和新生儿梗阻中都有一组 143 个转录本被调节,我们在短期梗阻(1 天)模型中测试了它们的表达,在该模型中,肾损伤是短暂和可逆的,而在长期梗阻(5 天)模型中,肾损伤是永久性的。大量转录本在梗阻后早期升高,随后恢复正常,而 26 个转录本在解除 5 天输尿管梗阻后 10 天和 28 天仍升高。通过 qPCR 检测,在梗阻小鼠的尿液中检测到几种候选 RNA 肾损伤生物标志物的水平升高。此外,在接受肾盂输尿管连接部梗阻手术的患儿的导尿样本中,也可检测到几种梗阻导致的候选 RNA 损伤生物标志物。测量对肾梗阻有反应的尿转录本可作为肾损伤的生物标志物,具有重要的临床应用价值。