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Processing of [D-Arg1,D-Phe5,D-Trp7,9,Leu11]substance P in xenograft bearing Nu/Nu mice.

作者信息

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

机构信息

Imperial Cancer Research Fund, Western General Hospital, Edinburgh, UK.

出版信息

Peptides. 1997;18(7):1073-7. doi: 10.1016/s0196-9781(97)00042-9.

DOI:10.1016/s0196-9781(97)00042-9
PMID:9357069
Abstract

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]Substance P is a broad-spectrum neuropeptide growth factor antagonist that has exhibited in vitro activity against a range of human cancer cell lines. The fate of this compound in vivo following i.p. administration at 12 micrograms/g to nu/nu mice bearing the H69 small-cell lung cancer xenograft has been studied. Metabolism was confined to the C-terminus producing [D-Arg1,D-Phe5,D-Trp7,9,Leu11]substance P acid and [D-Arg1,D-Phe5,D-Trp7,9]substance P(1-10). The peptide had a long half-life in plasma (45.9 min) and became widely distributed among the tissues studied with the highest accumulation observed in the liver (AUC 1102 micrograms/g x min) and the lowest in the brain (5 micrograms/g x min). Uptake into the tumor xenograft was poor (AUC 189 micrograms/g x min); however, uptake into the lungs was much greater (AUC 507 micrograms/g x min), offering encouragement that therapeutic concentrations may be targeted to primary lung tumors.

摘要

相似文献

1
Processing of [D-Arg1,D-Phe5,D-Trp7,9,Leu11]substance P in xenograft bearing Nu/Nu mice.
Peptides. 1997;18(7):1073-7. doi: 10.1016/s0196-9781(97)00042-9.
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
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]substance P, a potent bombesin antagonist in murine Swiss 3T3 cells, inhibits the growth of human small cell lung cancer cells in vitro.[D-精氨酸1,D-苯丙氨酸5,D-色氨酸7,9,亮氨酸11]P物质,一种在小鼠瑞士3T3细胞中有效的蛙皮素拮抗剂,可在体外抑制人小细胞肺癌细胞的生长。
Proc Natl Acad Sci U S A. 1988 Mar;85(6):1859-63. doi: 10.1073/pnas.85.6.1859.
4
Stability and in vitro metabolism of the mitogenic neuropeptide antagonists [D-Arg1,D-Phe5, D-Trp7,9, Leu11]-substance P and [Arg6, D-Trp7,9, MePhe8]-substance P (6-11) characterized by high-performance liquid chromatography.通过高效液相色谱法对促有丝分裂神经肽拮抗剂[D-精氨酸1,D-苯丙氨酸5,D-色氨酸7,9,亮氨酸11]-P物质和[精氨酸6,D-色氨酸7,9,甲基苯丙氨酸8]-P物质(6-11)的稳定性及体外代谢进行了表征。
J Pharm Biomed Anal. 1994 Jun;12(6):811-9. doi: 10.1016/0731-7085(93)e0027-k.
5
[D-Arg1, D-Phe5, D-Trp7,9, Leu11] substance P induces apoptosis in lung cancer cell lines in vitro.
Biochem Biophys Res Commun. 1994 Mar 30;199(3):1313-9. doi: 10.1006/bbrc.1994.1374.
6
[D-Arg1, D-Phe5, D-Trp7,9, Leu11] substance P inhibits the growth of human small cell lung cancer xenografts in vivo.
Eur J Cancer. 1993;29A(10):1450-3. doi: 10.1016/0959-8049(93)90019-c.
7
Metabolism of the broad-spectrum neuropeptide growth factor antagonist: [D-Arg1, D-Phe5, D-Trp7,9, Leu11]-substance P.广谱神经肽生长因子拮抗剂:[D-精氨酸1,D-苯丙氨酸5,D-色氨酸7,9,亮氨酸11] - P物质的代谢
Br J Cancer. 1996 Mar;73(6):715-20. doi: 10.1038/bjc.1996.126.
8
[D-Arg1,D-Trp5,7,9,Leu11]substance P: a novel potent inhibitor of signal transduction and growth in vitro and in vivo in small cell lung cancer cells.
Cancer Res. 1997 Jan 1;57(1):51-4.
9
Broad spectrum neuropeptide antagonists inhibit the growth of small cell lung cancer in vivo.
Cancer Res. 1992 Aug 15;52(16):4554-7.
10
Determination of two neuropeptide growth factor antagonists, [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-substance P and [Arg6,D-Trp7,9,N-MePhe8]- substance P(6-11), by high-performance liquid chromatography with electrochemical detection.
J Chromatogr B Biomed Appl. 1994 Mar 4;653(2):195-203. doi: 10.1016/0378-4347(93)e0442-s.

引用本文的文献

1
Increased gastrin-releasing peptide (GRP) receptor expression in tumour cells confers sensitivity to [Arg6,D-Trp7,9,NmePhe8]-substance P (6-11)-induced growth inhibition.肿瘤细胞中胃泌素释放肽(GRP)受体表达增加赋予了对[精氨酸6,D-色氨酸7,9,N-甲基苯丙氨酸8] -P物质(6-11)诱导的生长抑制的敏感性。
Br J Cancer. 2003 Jun 2;88(11):1808-16. doi: 10.1038/sj.bjc.6600957.