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2
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Reply: Urinary Excretion of MicroRNA-126 Is a Biomarker for Hemangioma Proliferation.回复:微小RNA - 126的尿排泄是血管瘤增殖的生物标志物。
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本文引用的文献

1
The role of miR-126 in embryonic angiogenesis, adult vascular homeostasis, and vascular repair and its alterations in atherosclerotic disease.miR-126在胚胎血管生成、成人血管稳态、血管修复中的作用及其在动脉粥样硬化疾病中的改变。
J Mol Cell Cardiol. 2016 Aug;97:47-55. doi: 10.1016/j.yjmcc.2016.05.007. Epub 2016 May 12.
2
Multidrug Resistance-associated Protein-1 (MRP-1)-dependent Glutathione Disulfide (GSSG) Efflux as a Critical Survival Factor for Oxidant-enriched Tumorigenic Endothelial Cells.多药耐药相关蛋白1(MRP-1)依赖性谷胱甘肽二硫化物(GSSG)外排作为富含氧化剂的致瘤性内皮细胞的关键生存因子。
J Biol Chem. 2016 May 6;291(19):10089-103. doi: 10.1074/jbc.M115.688879. Epub 2016 Mar 9.
3
Endothelial cell tumor growth is Ape/ref-1 dependent.内皮细胞肿瘤生长依赖于Ape/ref-1。
Am J Physiol Cell Physiol. 2015 Sep 1;309(5):C296-307. doi: 10.1152/ajpcell.00022.2015. Epub 2015 Jun 24.
4
A randomized, controlled trial of oral propranolol in infantile hemangioma.口服普萘洛尔治疗婴儿血管瘤的随机对照试验。
N Engl J Med. 2015 Feb 19;372(8):735-46. doi: 10.1056/NEJMoa1404710.
5
miR-126 modulates angiogenic growth parameters of peripheral blood endothelial progenitor cells.微小RNA-126调节外周血内皮祖细胞的血管生成生长参数。
Biol Chem. 2015 Mar;396(3):245-52. doi: 10.1515/hsz-2014-0259.
6
High-throughput screening of a CRISPR/Cas9 library for functional genomics in human cells.高通量筛选 CRISPR/Cas9 文库在人类细胞中的功能基因组学研究。
Nature. 2014 May 22;509(7501):487-91. doi: 10.1038/nature13166. Epub 2014 Apr 9.
7
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Cardiovasc Res. 2014 Jun 1;102(3):436-47. doi: 10.1093/cvr/cvu040. Epub 2014 Feb 21.
8
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J Biol Chem. 2014 Mar 28;289(13):9027-38. doi: 10.1074/jbc.M113.519264. Epub 2014 Feb 4.
9
MicroRNA-29c in urinary exosome/microvesicle as a biomarker of renal fibrosis.尿外泌体/微囊泡中的 microRNA-29c 作为肾纤维化的生物标志物。
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10
MicroRNAs: a new piece in the paediatric cardiovascular disease puzzle.微小RNA:小儿心血管疾病谜题中的新拼图。
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微小RNA-126的尿排泄是血管瘤增殖的生物标志物。

Urinary Excretion of MicroRNA-126 Is a Biomarker for Hemangioma Proliferation.

作者信息

Biswas Ayan, Pan Xueliang, Meyer Melissa, Khanna Savita, Roy Sashwati, Pearson Gregory, Kirschner Richard, Witman Patricia, Faith Esteban Fernandez, Sen Chandan K, Gordillo Gayle M

机构信息

Columbus, Ohio.

From the Department of Plastic Surgery, the Department of Biomedical Informatics, Center for Biostatistics, the Department of Surgery, and the Divisions of Vascular Surgery and General Surgery, The Ohio State University; and the Department of Pediatrics, the Hemangioma and Vascular Malformation Clinic, and the Department of Pediatrics, Division of Dermatology, Nationwide Children's Hospital.

出版信息

Plast Reconstr Surg. 2017 Jun;139(6):1277e-1284e. doi: 10.1097/PRS.0000000000003349.

DOI:10.1097/PRS.0000000000003349
PMID:28538565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5963954/
Abstract

BACKGROUND

Hemangiomas are unique endothelial cell tumors that involute spontaneously, which makes interpreting their response to therapies difficult. The objective of this work was to identify a potential biomarker in the urine of children with infantile hemangiomas that would facilitate testing new therapies.

METHODS

A prospective longitudinal study in children with hemangiomas and age-matched healthy controls was performed to determine whether microRNA-126, which is highly abundant in fetal endothelial cells, was more abundant in the urine of affected children. Prospective ultrasound measurements of hemangioma size and blood flow velocity were obtained as secondary endpoints to document longitudinal changes in untreated hemangiomas.

RESULTS

Urinary microRNA-126 levels were significantly elevated in children with proliferating hemangiomas, and relative levels of urinary microRNA abundance correlated with hemangioma size. Hemangiomas had elevated levels of microRNA abundance compared with healthy controls. Ultrasound data revealed that hemangioma proliferation typically stopped between 6 and 9 months of age. When hemangioma proliferation stopped, urinary microRNA-126 levels in children with hemangiomas dropped to levels observed in healthy age-matched controls.

CONCLUSIONS

These are the first reported results to identify a potential microRNA biomarker in the urine of children with hemangiomas. Measurement of urinary levels of microRNA-126 could potentially be used to monitor hemangioma response to therapies.

CLINICAL QUESTION/LEVEL OF EVIDENCE: Diagnostic, II.

摘要

背景

血管瘤是一种独特的内皮细胞瘤,可自发消退,这使得解读其对治疗的反应变得困难。本研究的目的是在患有婴儿血管瘤的儿童尿液中鉴定一种潜在的生物标志物,以促进新疗法的测试。

方法

对患有血管瘤的儿童和年龄匹配的健康对照进行了一项前瞻性纵向研究,以确定在胎儿内皮细胞中高度丰富的微小RNA-126在患病儿童尿液中是否更丰富。作为记录未经治疗的血管瘤纵向变化的次要终点,获得了血管瘤大小和血流速度的前瞻性超声测量结果。

结果

增殖期血管瘤患儿尿中微小RNA-126水平显著升高,尿中微小RNA丰度的相对水平与血管瘤大小相关。与健康对照相比,血管瘤的微小RNA丰度水平升高。超声数据显示,血管瘤增殖通常在6至9个月龄时停止。当血管瘤增殖停止时,患有血管瘤的儿童尿中微小RNA-126水平降至年龄匹配的健康对照者中观察到的水平。

结论

这些是首次报道的在患有血管瘤的儿童尿液中鉴定潜在微小RNA生物标志物的结果。测量尿中微小RNA-126水平可能用于监测血管瘤对治疗的反应。

临床问题/证据水平:诊断性,II级