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尿透明质酸是一种肾母细胞瘤标志物。

Urinary hyaluronic acid is a Wilms' tumor marker.

作者信息

Lin R Y, Argenta P A, Sullivan K M, Stern R, Adzick N S

机构信息

Fetal Treatment Center, University of California, San Francisco School of Medicine 94143-0570, USA.

出版信息

J Pediatr Surg. 1995 Feb;30(2):304-8. doi: 10.1016/0022-3468(95)90578-2.

DOI:10.1016/0022-3468(95)90578-2
PMID:7738755
Abstract

Wilms' tumor is a renal neoplasm that is histologically similar to fetal kidney tissue. Both Wilms' tumor and the fetal kidney have high levels of the glycosaminoglycan hyaluronic acid (HA) in the extracellular matrix. Preliminary studies suggest that urinary HA levels are elevated in Wilms' tumor patients. To test the utility of urinary HA as a Wilms' tumor marker, the authors compared HA levels in urine specimens from 105 Wilms' tumor patients with those of 17 age-matched controls. Preoperative urine samples (n = 92), early postoperative samples, obtained from 1 to 3 weeks after surgery (n = 63), and late postoperative samples, obtained from 1 to 6 months after surgery (n = 58) were collected from patients at 30 institutions between 1989 and 1993. The HA levels were determined in triplicate by a competitive enzyme-linked immunosorbent binding assay. Seventy-four percent of the preoperative urine specimens contained elevated HA levels compared with the controls. The preoperative HA levels were significantly higher than the early postoperative (P < .01), late postoperative (P < .01), and control levels (P < .01). There was significant correlation between preoperative HA levels and clinical tumor staging. The mean preoperative HA level for patients with histological evidence of nephroblastomatosis was higher than that for patients without nephroblastomatosis. In the late postoperative period, patients with relapse or persistent disease had higher levels of urinary HA than did the disease-free patients (P < .05). In Wilms' tumor patients, urinary HA levels are elevated preoperatively and decline progressively after surgery.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肾母细胞瘤是一种组织学上与胎儿肾组织相似的肾脏肿瘤。肾母细胞瘤和胎儿肾在细胞外基质中都含有高水平的糖胺聚糖透明质酸(HA)。初步研究表明,肾母细胞瘤患者尿HA水平升高。为了测试尿HA作为肾母细胞瘤标志物的效用,作者比较了105例肾母细胞瘤患者尿液标本中的HA水平与17例年龄匹配的对照者的HA水平。1989年至1993年期间,从30个机构的患者中收集了术前尿样(n = 92)、术后早期样本(术后1至3周,n = 63)和术后晚期样本(术后1至6个月,n = 58)。通过竞争性酶联免疫吸附结合试验一式三份测定HA水平。与对照组相比,74%的术前尿标本HA水平升高。术前HA水平显著高于术后早期(P <.01)、术后晚期(P <.01)和对照水平(P <.01)。术前HA水平与临床肿瘤分期之间存在显著相关性。有肾母细胞瘤组织学证据的患者术前HA平均水平高于无肾母细胞瘤的患者。在术后晚期,复发或持续存在疾病的患者尿HA水平高于无疾病患者(P <.05)。在肾母细胞瘤患者中,术前尿HA水平升高,术后逐渐下降。(摘要截短至250字)

相似文献

1
Urinary hyaluronic acid is a Wilms' tumor marker.尿透明质酸是一种肾母细胞瘤标志物。
J Pediatr Surg. 1995 Feb;30(2):304-8. doi: 10.1016/0022-3468(95)90578-2.
2
Diagnostic and prognostic role of basic fibroblast growth factor in Wilms' tumor patients.
Clin Cancer Res. 1995 Mar;1(3):327-31.
3
Prohibitin is a prognostic marker and therapeutic target to block chemotherapy resistance in Wilms' tumor.抑制素是一种预后标志物和治疗靶点,可阻断肾母细胞瘤的化疗耐药性。
JCI Insight. 2019 Aug 8;4(15). doi: 10.1172/jci.insight.127098.
4
Glycosaminoglycan structure and content differ according to the origins of human tumors.糖胺聚糖的结构和含量因人类肿瘤的起源而异。
Braz J Med Biol Res. 1994 Sep;27(9):2253-8.
5
Hyaluronic acid-stimulating activity in the pathophysiology of Wilms' tumors.透明质酸刺激活性在肾母细胞瘤病理生理学中的作用
J Natl Cancer Inst. 1990 Jan 17;82(2):135-9. doi: 10.1093/jnci/82.2.135.
6
Hyaluronidase levels in urine from Wilms' tumor patients.肾母细胞瘤患者尿液中的透明质酸酶水平。
J Natl Cancer Inst. 1991 Nov 6;83(21):1569-74. doi: 10.1093/jnci/83.21.1569.
7
Sera of children with renal tumours contain low-molecular-mass hyaluronic acid.患有肾肿瘤的儿童血清中含有低分子量透明质酸。
Int J Cancer. 1989 Sep 15;44(3):445-8. doi: 10.1002/ijc.2910440311.
8
Glycosaminoglycan synthesis by Wilms' tumor.肾母细胞瘤的糖胺聚糖合成
Pediatr Res. 1978 Jan;12(1):52-6. doi: 10.1203/00006450-197801000-00013.
9
The nephroblastomatosis complex and its relationship to Wilms' tumor: a clinicopathologic treatise.肾母细胞瘤病复合体及其与肾母细胞瘤的关系:一篇临床病理学论文
Perspect Pediatr Pathol. 1976;3:185-223.
10
[Nephroblastomatosis: a precancerous condition of Wilms' tumor].肾母细胞瘤病:一种肾母细胞瘤的癌前状态
Aktuelle Radiol. 1994 Jul;4(4):195-7.

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JCI Insight. 2019 Aug 8;4(15). doi: 10.1172/jci.insight.127098.
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