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用一种新型S-腺苷甲硫氨酸脱羧酶抑制剂4-脒基茚-1-酮-2'-脒基腙处理裸鼠,可延缓人黑色素瘤细胞的生长并抑制其转移。

Treatment of nude mice with 4-amidinoindan -1- one2 '- amidinohydrazone, a new S-adenosylmethionine decarboxylase inhibitor, delays growth and inhibits metastasis of human melanoma cells.

作者信息

Gutman M, Beltran P J, Fan D, Delworth M G, Singh R K, Wilson M R, Fidler I J

机构信息

Department of Cell Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Melanoma Res. 1995 Jun;5(3):147-54. doi: 10.1097/00008390-199506000-00002.

DOI:10.1097/00008390-199506000-00002
PMID:7640515
Abstract

CGP 48664A (4-amidinoindan-1-one2'-amidinohydrazone) is a novel inhibitor of S-adenosyl-methionine decarboxylase (SAMDC), a key enzyme in the biosynthesis of polyamines, which are themselves essential for proliferation of mammalian cells. Seven different human melanoma cell lines were treated in vitro with CGP 48664A. High, intermediate and low levels of cytostasis were induced in four, one and two melanoma lines, respectively. This cytostasis was reversed by the addition of exogenous spermidine or spermine to the culture medium. The heterogeneous low metastatic (CGP 48664A-resistant) A375P cells and highly metastatic (CGP 48664A-sensitive) A375SM cells were implanted into the subcutis or injected intravenously into nude mice. Systemic daily administration of CGP 48664A significantly reduced the size of cutaneous lesions and the number of lung metastases in mice implanted with A375SM cells. No beneficial effects were found in mice injected with A375P cells. Drug activity was dose dependent, and maximal effects were observed when treatment began in mice with small tumour burdens. The data suggest that CGP 48664A is effective against melanoma metastasis in nude mice and that its activity should be tested in combination with other cytoreductive agents.

摘要

CGP 48664A(4-脒基茚满-1-酮2'-脒基腙)是S-腺苷甲硫氨酸脱羧酶(SAMDC)的新型抑制剂,SAMDC是多胺生物合成中的关键酶,而多胺本身对于哺乳动物细胞的增殖至关重要。七种不同的人黑色素瘤细胞系在体外用CGP 48664A处理。在四种、一种和两种黑色素瘤细胞系中分别诱导出高水平、中等水平和低水平的细胞生长停滞。向培养基中添加外源性亚精胺或精胺可逆转这种细胞生长停滞。将低转移异质性(对CGP 48664A耐药)的A375P细胞和高转移(对CGP 48664A敏感)的A375SM细胞植入皮下或静脉注射到裸鼠体内。每天全身性给予CGP 48664A可显著减小植入A375SM细胞的小鼠皮肤损伤的大小和肺转移灶的数量。在注射A375P细胞的小鼠中未发现有益效果。药物活性呈剂量依赖性,在肿瘤负荷较小的小鼠中开始治疗时观察到最大效果。数据表明,CGP 48664A对裸鼠黑色素瘤转移有效,其活性应与其他减瘤剂联合测试。

相似文献

1
Treatment of nude mice with 4-amidinoindan -1- one2 '- amidinohydrazone, a new S-adenosylmethionine decarboxylase inhibitor, delays growth and inhibits metastasis of human melanoma cells.用一种新型S-腺苷甲硫氨酸脱羧酶抑制剂4-脒基茚-1-酮-2'-脒基腙处理裸鼠,可延缓人黑色素瘤细胞的生长并抑制其转移。
Melanoma Res. 1995 Jun;5(3):147-54. doi: 10.1097/00008390-199506000-00002.
2
4-Amidinoindan-1-one 2'-amidinohydrazone (CGP 48664A) exerts in vitro growth inhibitory effects that are not only related to S-adenosylmethionine decarboxylase (SAMdc) inhibition.4-脒基茚满-1-酮2'-脒基腙(CGP 48664A)发挥体外生长抑制作用,这种作用不仅与抑制S-腺苷甲硫氨酸脱羧酶(SAMdc)有关。
Biochim Biophys Acta. 1997 Apr 17;1335(1-2):144-52. doi: 10.1016/s0304-4165(96)00134-1.
3
In vivo growth inhibition of L1210 leukemia by 4-amidinoindan-1-one 2'-amidinohydrazone (CGP 48664A), a new inhibitor of S-adenosylmethionine decarboxylase.新型S-腺苷甲硫氨酸脱羧酶抑制剂4-脒基茚满-1-酮2'-脒基腙(CGP 48664A)对L1210白血病的体内生长抑制作用
Int J Cancer. 1995 Apr 10;61(2):214-7. doi: 10.1002/ijc.2910610212.
4
CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity.CGP 48664,一种新型的具有广谱抗增殖和抗肿瘤活性的S-腺苷甲硫氨酸脱羧酶抑制剂。
Cancer Res. 1994 Jun 15;54(12):3210-7.
5
In vivo effects of 4-amidinoindan-1-one 2'-amidinohydrazone (CGP 48664A) and alpha-difluoromethylornithine (DFMO) on L1210 growth, cell-cycle phase distribution and polyamine contents.4-脒基茚满-1-酮2'-脒基腙(CGP 48664A)和α-二氟甲基鸟氨酸(DFMO)对L1210细胞生长、细胞周期阶段分布及多胺含量的体内效应
Int J Cancer. 1995 Sep 15;62(6):738-42. doi: 10.1002/ijc.2910620615.
6
CGP 48664, a potent and specific S-adenosylmethionine decarboxylase inhibitor: effects on regulation and stability of the enzyme.CGP 48664,一种强效且特异性的S-腺苷甲硫氨酸脱羧酶抑制剂:对该酶调节和稳定性的影响。
Biochem J. 1997 Feb 15;322 ( Pt 1)(Pt 1):297-302. doi: 10.1042/bj3220297.
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Biochemical and growth-modulatory effects of the new S-adenosylmethionine decarboxylase inhibitor CGP 48664 in malignant and immortalized normal human breast epithelial cells in culture.新型S-腺苷甲硫氨酸脱羧酶抑制剂CGP 48664对培养的恶性及永生化正常人乳腺上皮细胞的生化及生长调节作用
Int J Cancer. 1995 Aug 9;62(4):485-91. doi: 10.1002/ijc.2910620421.
8
Systemic administration of 4-amidinoindanon-1-(2'-amidino)-hydrazone, a new inhibitor of s-adenosylmethionine decarboxylase, produces cytostasis of human prostate-cancer in athymic nude-mice.新型S-腺苷甲硫氨酸脱羧酶抑制剂4-脒基茚满-1-(2'-脒基)腙的全身给药可使无胸腺裸鼠体内的人前列腺癌产生细胞生长停滞。
Int J Oncol. 1995 Feb;6(2):293-9. doi: 10.3892/ijo.6.2.293.
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Collateral sensitivity of human melanoma multidrug-resistant variants to the polyamine analogue, N1,N11-diethylnorspermine.人黑色素瘤多药耐药变体对多胺类似物N1,N11-二乙基亚精胺的 collateral 敏感性 。 注:这里“collateral”不太好准确翻译,结合语境大概是指一种相关或附带的敏感性,可根据具体专业知识进一步理解其确切含义。
Cancer Res. 1994 Nov 15;54(22):5917-24.
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Lysosomal sequestration of polyamine analogues in Chinese hamster ovary cells resistant to the S-adenosylmethionine decarboxylase inhibitor, CGP-48664.多胺类似物在对S-腺苷甲硫氨酸脱羧酶抑制剂CGP-48664具有抗性的中国仓鼠卵巢细胞中的溶酶体隔离
Cancer Res. 1998 Sep 1;58(17):3883-90.

引用本文的文献

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Multi-centre Phase II trial of the polyamine synthesis inhibitor SAM486A (CGP48664) in patients with metastatic melanoma.多胺合成抑制剂SAM486A(CGP48664)用于转移性黑色素瘤患者的多中心II期试验。
Invest New Drugs. 2005 Jun;23(3):253-6. doi: 10.1007/s10637-005-6734-z.
2
c-Jun activation-dependent tumorigenic transformation induced paradoxically by overexpression or block of S-adenosylmethionine decarboxylase.S-腺苷甲硫氨酸脱羧酶的过表达或阻断反常地诱导c-Jun激活依赖性致瘤转化。
J Cell Biol. 2000 Nov 13;151(4):801-10. doi: 10.1083/jcb.151.4.801.
3
A phase I study of a new polyamine biosynthesis inhibitor, SAM486A, in cancer patients with solid tumours.
一种新型多胺生物合成抑制剂SAM486A在实体瘤癌症患者中的I期研究。
Br J Cancer. 2000 Sep;83(5):594-601. doi: 10.1054/bjoc.2000.1305.