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在小鼠肿瘤发展过程中,修饰核苷和碱基的尿液水平不断升高。

Increasing urinary levels of modified nucleosides and bases during tumor development in mice.

作者信息

Thomale J, Nass G

出版信息

Recent Results Cancer Res. 1983;84:378-87. doi: 10.1007/978-3-642-81947-6_28.

Abstract

Based on the fact that human cancer patients excrete increased amounts of various modified nucleosides and bases in their urine, we investigated whether the same phenomenon takes place in mice bearing experimentally induced tumors. We did indeed find that mice with MCA-induced skin tumors and mice exhibiting leukemia after X-ray irradiation excrete severalfold higher levels of modified nucleosides and bases than do untreated control mice. Comparison of the time course of altered urinary excretion of these RNA catabolites with the appearance of a recognizable tumor after MCA application revealed that the onset of the altered excretion rate of these compounds precedes tumor diagnosis. At present, the time-course studies in our mice exposed to a single X-ray dose to induce lymphoblastic leukemia seem to indicate a similar situation. Mice exhibiting preleukemic histological features already excrete increased amounts of various modified nucleosides and bases. Confirmation of our results by analysis of further irradiation-exposed mice in our present detailed time-course studies and of tumors experimentally induced in other organs of mice and other species will be taken as a basis for developing an in vivo test for carcinogenicity. Furthermore, the results could provide a foundation for the setting up of a noninvasive, early screening method for cancer in human beings.

摘要

基于人类癌症患者尿液中各种修饰核苷和碱基的排泄量增加这一事实,我们研究了在实验诱导肿瘤的小鼠中是否会发生同样的现象。我们确实发现,患有MCA诱导的皮肤肿瘤的小鼠以及经X射线照射后出现白血病的小鼠,其修饰核苷和碱基的排泄水平比未处理的对照小鼠高出数倍。将这些RNA分解代谢物尿液排泄变化的时间进程与MCA应用后可识别肿瘤的出现进行比较,发现这些化合物排泄率变化的开始先于肿瘤诊断。目前,我们对接受单次X射线照射以诱导淋巴细胞白血病的小鼠进行的时间进程研究似乎表明情况类似。表现出白血病前期组织学特征的小鼠已经排泄出增加量的各种修饰核苷和碱基。通过在我们目前详细的时间进程研究中对更多受照射小鼠进行分析,以及对在小鼠和其他物种的其他器官中实验诱导的肿瘤进行分析来证实我们的结果,将作为开发体内致癌性测试的基础。此外,这些结果可为建立一种针对人类癌症的非侵入性早期筛查方法提供基础。

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