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酶联免疫吸附测定法检测健康供体和癌症患者血液中的可溶性尿激酶受体

ELISA determination of soluble urokinase receptor in blood from healthy donors and cancer patients.

作者信息

Stephens R W, Pedersen A N, Nielsen H J, Hamers M J, Høyer-Hansen G, Rønne E, Dybkjaer E, Danø K, Brünner N

机构信息

The Finsen Laboratory, Rigshospitalet, Copenhagen, Denmark.

出版信息

Clin Chem. 1997 Oct;43(10):1868-76.

PMID:9342006
Abstract

Measurement of urokinase receptor (uPAR) in tumor extracts has prognostic value, but assay of the soluble uPAR (suPAR) in peripheral blood may offer wider applications in cancer patient management. A tumor extract uPAR ELISA was modified to eliminate nonspecific plasma protein interference, enabling specific detection of suPAR in plasma and sera with >90% recovery of added calibrator. suPAR concentrations in citrate plasma correlated with sera in 93 healthy blood donors (r = 0.84, P <0.0001), with a median value for both of 1.2 microg/L. The plasma median for 19 advanced breast cancer patients was 2.9 microg/L suPAR, and a similar increase was found for 10 advanced colon cancer patients, consistent with release of suPAR from tumors into blood. Repetitive monitoring of suPAR in cancer patients' blood may have value in assessment of prognosis and tumor recurrence.

摘要

在肿瘤提取物中测量尿激酶受体(uPAR)具有预后价值,但检测外周血中的可溶性uPAR(suPAR)可能在癌症患者管理中有更广泛的应用。对肿瘤提取物uPAR ELISA进行了改进,以消除非特异性血浆蛋白干扰,从而能够特异性检测血浆和血清中的suPAR,添加的校准物回收率>90%。93名健康献血者的枸橼酸盐血浆中suPAR浓度与血清相关(r = 0.84,P <0.0001),两者的中位数均为1.2 μg/L。19例晚期乳腺癌患者的血浆中位数为2.9 μg/L suPAR,10例晚期结肠癌患者也有类似升高,这与suPAR从肿瘤释放到血液中一致。对癌症患者血液中的suPAR进行重复监测可能对评估预后和肿瘤复发有价值。

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