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[合成亮氨酸脑啡肽类似物达乐argin对致癌作用的抑制效应]

[The inhibitory effect of the synthetic leu-enkephalin analog dalargin on carcinogenesis].

作者信息

Anisimov V N, Bortkevich S M

出版信息

Vopr Onkol. 1990;36(5):556-9.

PMID:2378078
Abstract

Dalargin, an opioid peptide (Tyr-D-Ala-Gly-Phe-Leu-Arg), was shown to significantly inhibit the carcinogenic effect of 50 mg/kg body weight nitrosomethylurea given as single i. v. infection. The treatment was followed by an increase in the tumor latency period. Moreover, the overall incidence of tumors decreased by 20% whereas that of malignant neoplasms and breast adenocarcinoma--by 33 and 27%, respectively. Pronounced inhibitory effect of dalargin on hematopoietic tumor induction was identified, too.

摘要

达乐argin(一种阿片肽,酪氨酸-D-丙氨酸-甘氨酸-苯丙氨酸-亮氨酸-精氨酸)已被证明能显著抑制单次静脉注射给予50毫克/千克体重的亚硝基甲基脲的致癌作用。治疗后肿瘤潜伏期延长。此外,肿瘤的总体发生率下降了20%,而恶性肿瘤和乳腺腺癌的发生率分别下降了33%和27%。还发现达乐argin对造血系统肿瘤的诱导有明显的抑制作用。

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