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关于广谱神经肽生长因子拮抗剂G的临床前研究。

Preclinical studies on the broad-spectrum neuropeptide growth factor antagonist G.

作者信息

Jones D A, Cummings J, Langdon S P, Smyth J F

机构信息

Imperial Cancer Research Fund, Medical Oncology Unit, Western General Hospital, Edinburgh, UK.

出版信息

Gen Pharmacol. 1997 Feb;28(2):183-9. doi: 10.1016/s0306-3623(96)00189-9.

Abstract
  1. Antagonist G is a broad-spectrum neuropeptide growth factor antagonist that inhibits the growth of small cell lung cancer (SCLC) cells both in vitro and in vivo. 2. Antagonist G is metabolized in peripheral tissues by a chymotrypsin-like serine carboxypeptidase causing C-terminal deamidation and removal of the methionine residue. 3. The metabolites of Antagonist G retain neuropeptide antagonist properties and are thought to contribute to the parent peptide's antitumor activity. 4. Pharmacokinetic studies following systemic (IP) administration to nude mice revealed that the tissue distribution of Antagonist G is likely to be determined by vascular permeability. 5. Preclinical toxicology studies have been completed, and we have now started a phase I clinical trial.
摘要
  1. 拮抗剂G是一种广谱神经肽生长因子拮抗剂,在体外和体内均能抑制小细胞肺癌(SCLC)细胞的生长。2. 拮抗剂G在外周组织中被一种类胰凝乳蛋白酶丝氨酸羧肽酶代谢,导致C末端脱酰胺并去除甲硫氨酸残基。3. 拮抗剂G的代谢产物保留神经肽拮抗剂特性,被认为有助于母体肽的抗肿瘤活性。4. 对裸鼠进行全身(腹腔内)给药后的药代动力学研究表明,拮抗剂G的组织分布可能由血管通透性决定。5. 临床前毒理学研究已经完成,我们现已开始一期临床试验。

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