• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/s0306-3623(96)00189-9
PMID:9013192
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。

相似文献

1
Preclinical studies on the broad-spectrum neuropeptide growth factor antagonist G.关于广谱神经肽生长因子拮抗剂G的临床前研究。
Gen Pharmacol. 1997 Feb;28(2):183-9. doi: 10.1016/s0306-3623(96)00189-9.
2
Pharmacokinetics, metabolism, tissue and tumour distribution of the neuropeptide growth factor antagonist [Arg6, D-Trp7,9, NmePhe8]- substance P(6-11) in nude mice bearing the H69 small-cell lung cancer xenograft.神经肽生长因子拮抗剂[精氨酸6,D-色氨酸7,9,去甲苯丙氨酸8]-P物质(6-11)在携带H69小细胞肺癌异种移植瘤的裸鼠体内的药代动力学、代谢、组织及肿瘤分布
Ann Oncol. 1995 Jul;6(6):595-602. doi: 10.1093/oxfordjournals.annonc.a059250.
3
Bradykinin antagonist dimer, CU201, inhibits the growth of human lung cancer cell lines in vitro and in vivo and produces synergistic growth inhibition in combination with other antitumor agents.缓激肽拮抗剂二聚体CU201在体外和体内均能抑制人肺癌细胞系的生长,并与其他抗肿瘤药物联合使用时产生协同生长抑制作用。
Clin Cancer Res. 2002 May;8(5):1280-7.
4
[Arg6,D-Trp7,9,NmePhe8]-substance P (6-11) activates JNK and induces apoptosis in small cell lung cancer cells via an oxidant-dependent mechanism.[精氨酸6、D-色氨酸7、9、N-甲基苯丙氨酸8] -P物质(6-11)通过一种依赖氧化剂的机制激活JNK并诱导小细胞肺癌细胞凋亡。
Br J Cancer. 1999 Jun;80(7):1026-34. doi: 10.1038/sj.bjc.6690458.
5
[Arg(6), D-Trp(7,9), N(me)Phe(8)]-substance P (6-11) (antagonist G) induces AP-1 transcription and sensitizes cells to chemotherapy.[精氨酸(6)、D-色氨酸(7,9)、N-甲基苯丙氨酸(8)]-P物质(6-11)(拮抗剂G)诱导AP-1转录并使细胞对化疗敏感。
Br J Cancer. 2000 Oct;83(7):941-8. doi: 10.1054/bjoc.2000.1362.
6
Broad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivo.
Cancer Res. 1992 Aug 15;52(16):4554-7.
7
Effects of somatostatin analogue RC-160 and bombesin/gastrin-releasing peptide antagonists on the growth of human small-cell and non-small-cell lung carcinomas in nude mice.生长抑素类似物RC - 160及蛙皮素/胃泌素释放肽拮抗剂对裸鼠人小细胞和非小细胞肺癌生长的影响
Br J Cancer. 1994 Nov;70(5):886-92. doi: 10.1038/bjc.1994.415.
8
FK317, a novel substituted dihydrobenzoxazine, exhibits potent antitumor activity against human tumor xenografts in nude mice.FK317是一种新型的取代二氢苯并恶嗪,对裸鼠体内的人肿瘤异种移植瘤具有强大的抗肿瘤活性。
Jpn J Cancer Res. 1998 Dec;89(12):1306-17. doi: 10.1111/j.1349-7006.1998.tb00528.x.
9
New short-chain analogs of a substance-P antagonist inhibit proliferation of human small-cell lung-cancer cells in vitro and in vivo.
Int J Cancer. 1995 Jan 3;60(1):82-7. doi: 10.1002/ijc.2910600112.
10
Metabolism of the anticancer peptide H-Arg-D-Trp-NmePhe-D-Trp-Leu-Met-NH2.抗癌肽H-Arg-D-Trp-NmePhe-D-Trp-Leu-Met-NH2的代谢
Peptides. 1995;16(5):777-83. doi: 10.1016/0196-9781(95)00048-o.

引用本文的文献

1
Fungal Aflatoxins Reduce Respiratory Mucosal Ciliary Function.真菌黄曲霉毒素降低呼吸道黏膜纤毛功能。
Sci Rep. 2016 Sep 14;6:33221. doi: 10.1038/srep33221.
2
Increased expression of preprotachykinin-I and neurokinin receptors in human breast cancer cells: implications for bone marrow metastasis.人乳腺癌细胞中前速激肽原-I和神经激肽受体表达增加:对骨髓转移的影响
Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):388-93. doi: 10.1073/pnas.97.1.388.