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Lymphotropic accumulation of an antitumor antibiotic protein, neocarzinostatin.

作者信息

Maeda H, Takeshita J, Yamashita A

出版信息

Eur J Cancer (1965). 1980 May;16(5):723-31. doi: 10.1016/0014-2964(80)90215-7.

DOI:10.1016/0014-2964(80)90215-7
PMID:6446456
Abstract
摘要

相似文献

1
Lymphotropic accumulation of an antitumor antibiotic protein, neocarzinostatin.抗肿瘤抗生素蛋白新制癌菌素的亲淋巴细胞性蓄积
Eur J Cancer (1965). 1980 May;16(5):723-31. doi: 10.1016/0014-2964(80)90215-7.
2
Pharmacokinetics of the protein antitumor antibiotic neocarzinostatin after bolus injection in humans.蛋白质类抗肿瘤抗生素新制癌菌素在人体静脉推注后的药代动力学。
Cancer Res. 1979 Mar;39(3):757-61.
3
Pharmacokinetic analysis of neocarzinostatin in normal and tumor-bearing rodents.
Cancer Res. 1979 May;39(5):1547-51.
4
In vitro mode of action, pharmacokinetics, and organ specificity of poly (maleic acid-styrene)-conjugated neocarzinostatin, SMANCS.聚（马来酸-苯乙烯）共轭新制癌菌素（SMANCS）的体外作用模式、药代动力学及器官特异性
Gan. 1982 Apr;73(2):278-84.
5
[Study on the localization of neocarzinostatin in various tissues by enzyme-labeled antibody method--with special reference to the distribution into oral region (author's transl)].用酶标抗体法研究新制癌菌素在各种组织中的定位——特别参考其在口腔区域的分布（作者译）
Kokubyo Gakkai Zasshi. 1981 Mar;48(1):1-12.
6
Degradation of neocarzinostatin by blood sera in vitro and its inhibition by diisopropyl fluorophosphate and n-ethylmaleimide.
Gan. 1975 Oct;66(5):523-7.
7
Mechanism of accumulation of the antitumor protein antibiotic neocarzinostatin in bladder tissue: intravenous administration, urinary excretion, and absorption into bladder tissue.抗肿瘤蛋白抗生素新制癌菌素在膀胱组织中蓄积的机制：静脉给药、尿液排泄及膀胱组织吸收
Antimicrob Agents Chemother. 1977 Jun;11(6):941-5. doi: 10.1128/AAC.11.6.941.
8
[Studies on the stability of antitumor protein, neocarzinostatin. II. Stability of injection of neocarzinostatin (author's transl)].[抗肿瘤蛋白新制癌菌素的稳定性研究。II. 新制癌菌素注射液的稳定性（作者译）]
Jpn J Antibiot. 1974 Dec;27(6):715-24.
9
[Experimental study of intralymphatic chemotherapy in rabbits].[兔淋巴管内化疗的实验研究]
Gan To Kagaku Ryoho. 1987 Jul;14(7):2262-8.
10
Electron spin resonance detection of free radicals in the mercaptan-activation and UV-inactivation of neocarzinostatin.新制癌菌素的硫醇活化和紫外线灭活过程中自由基的电子自旋共振检测
Biochem Biophys Res Commun. 1981 Mar 16;99(1):213-20. doi: 10.1016/0006-291x(81)91734-4.

引用本文的文献

1
Analyses of repeated failures in cancer therapy for solid tumors: poor tumor-selective drug delivery, low therapeutic efficacy and unsustainable costs.实体瘤癌症治疗中反复失败的分析：肿瘤选择性药物递送不佳、治疗效果低以及成本难以持续。
Clin Transl Med. 2018 Mar 1;7(1):11. doi: 10.1186/s40169-018-0185-6.
2
Vascular permeability in cancer and infection as related to macromolecular drug delivery, with emphasis on the EPR effect for tumor-selective drug targeting.癌症和感染中的血管通透性与大分子药物递送的关系，重点是 EPR 效应在肿瘤选择性药物靶向中的作用。
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(3):53-71. doi: 10.2183/pjab.88.53.
3
Regiospecific O-methylation of naphthoic acids catalyzed by NcsB1, an O-methyltransferase involved in the biosynthesis of the enediyne antitumor antibiotic neocarzinostatin.
由NcsB1催化的萘甲酸区域特异性O-甲基化反应，NcsB1是一种参与烯二炔类抗肿瘤抗生素新制癌菌素生物合成的O-甲基转移酶。
J Biol Chem. 2008 May 23;283(21):14694-702. doi: 10.1074/jbc.M802206200. Epub 2008 Apr 3.
4
A pharmacokinetic simulation model for chemotherapy of brain tumor with an antitumor protein antibiotic, neocarzinostatin. Theoretical considerations behind a two-compartment model for continuous infusion via an internal carotid artery.一种使用抗肿瘤蛋白抗生素新制癌菌素进行脑肿瘤化疗的药代动力学模拟模型。经颈内动脉持续输注的双室模型背后的理论考量。
Cancer Chemother Pharmacol. 1981;5(4):243-9. doi: 10.1007/BF00434392.