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尿次黄嘌呤和假尿苷作为间皮瘤移植裸鼠肿瘤发展的指标。

Urinary hypoxanthine and pseudouridine as indicators of tumor development in mesothelioma-transplanted nude mice.

作者信息

Buhl L, Dragsholt C, Svendsen P, Hage E, Buhl M R

出版信息

Cancer Res. 1985 Mar;45(3):1159-62.

PMID:3838262
Abstract

A human mesothelioma was heterotransplanted to nude mice, and the urinary excretions of hypoxanthine, xanthine, pseudouridine, orotic acid, 7-methylguanine, and 1-methylhypoxanthine have been followed before and after the tumor transplantation. The compounds were measured by means of isotachophoresis, which has been found a rapid and precise method. The tumor reached maximum size within 30 days, and at this time a significantly increased excretion of pseudouridine and hypoxanthine was observed. Tumor growth was stopped by chemotherapy (vincristine, cyclophosphamide, prednisolone, and Adriamycin), and corresponding to this, a decrease occurred in both pseudouridine and hypoxanthine excretion to normal values.

摘要

将人恶性间皮瘤异种移植到裸鼠体内,在肿瘤移植前后对次黄嘌呤、黄嘌呤、假尿嘧啶核苷、乳清酸、7-甲基鸟嘌呤和1-甲基次黄嘌呤的尿排泄情况进行了跟踪研究。这些化合物通过等速电泳法进行测定,该方法已被证明是一种快速且精确的方法。肿瘤在30天内达到最大尺寸,此时观察到假尿嘧啶核苷和次黄嘌呤的排泄量显著增加。化疗(长春新碱、环磷酰胺、泼尼松龙和阿霉素)使肿瘤生长停止,相应地,假尿嘧啶核苷和次黄嘌呤的排泄量均降至正常值。

相似文献

1
Urinary hypoxanthine and pseudouridine as indicators of tumor development in mesothelioma-transplanted nude mice.尿次黄嘌呤和假尿苷作为间皮瘤移植裸鼠肿瘤发展的指标。
Cancer Res. 1985 Mar;45(3):1159-62.
2
[Pseudouridine excretion in patients with chronic renal insufficiency and in persons with transplanted kidney under the effect of immunosuppression].[慢性肾功能不全患者及免疫抑制作用下肾移植受者的假尿苷排泄情况]
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Response to doxorubicin and cyclophosphamide of a human pleural mesothelioma clinically and as a xenograft in nude rats.人胸膜间皮瘤对阿霉素和环磷酰胺的临床反应以及作为裸鼠异种移植瘤的反应。
In Vivo. 1990 Jan-Feb;4(1):55-9.
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[Usefulness of LDH isozyme for monitoring the therapy of human breast cancer transplanted in nude mice].[乳酸脱氢酶同工酶在监测裸鼠移植人乳腺癌治疗中的应用价值]
Gan To Kagaku Ryoho. 1984 Feb;11(2):270-8.
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[Interrelationship of pseudouridine and transfer RNA metabolic disorders in thermal injury].[热损伤中假尿苷与转运RNA代谢紊乱的相互关系]
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BMC Cancer. 2010 Feb 23;10:55. doi: 10.1186/1471-2407-10-55.