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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.

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。

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