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血清中的L-天冬酰胺合成酶作为肿瘤形成的标志物。

L-Asparagine synthetase in serum as a marker for neoplasia.

作者信息

Cooney D A, King V D, Cable R G, Taylor B, Wodinsky I

出版信息

Cancer Res. 1976 Sep;36(9 pt.1):3238-45.

PMID:10081
Abstract

L-Asparagine synthetase appears in serum approximately 7 days after the s.c. implantation of 1 X 10(5) cells of Leukemia 5178Y/AR (resistant to L-asparaginase) and increases in activity as the neoplasm grows and metastasizes. The principal source of the enzyme is the primary tumor. After intravranial inoculation of tumor, the rate of leakage of the enzyme is more pronounced than when the subcutaneous, intramuscular, or intraperitoneal routes are used. 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (NSC 79037), a nitro-sourea effective in the palliation of L5178Y/AR, temporarily halts the influx of enzyme into the blood stream, as does surgical excision of the s.c. tumor nodules. Treatment of mice with L-asparaginase within 24 hr of inoculation of the tumor markedly augments both tumor growth and the rate of penetration of L-asparagine synthetase into the circulation. Several other L-asparagine synthetase into the circulation. Several other L-asparaginase-resistant tumors also were found to spill L-asparagine synthetase into the serum, but the correlation between this phenomenon and the specific activity of the enzyme in homogenates of the tumor was imperfect.

摘要

在皮下接种1×10⁵个白血病5178Y/AR(对天冬酰胺酶耐药)细胞后约7天,血清中出现L-天冬酰胺合成酶,其活性随着肿瘤生长和转移而增加。该酶的主要来源是原发性肿瘤。肿瘤颅内接种后,酶的渗漏率比采用皮下、肌肉或腹腔途径时更为明显。1-(2-氯乙基)-3-环己基-1-亚硝基脲(NSC 79037),一种对缓解L5178Y/AR有效的亚硝基脲,会暂时阻止酶流入血流,皮下肿瘤结节的手术切除也有同样效果。在接种肿瘤后24小时内用天冬酰胺酶治疗小鼠,会显著促进肿瘤生长以及L-天冬酰胺合成酶进入循环的速率。还发现其他几种对天冬酰胺酶耐药的肿瘤也会将L-天冬酰胺合成酶释放到血清中,但这种现象与肿瘤匀浆中该酶的比活性之间的相关性并不完美。

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