• 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

[米诺环素对多种肿瘤细胞系的体外生长抑制活性]

[Growth-inhibitory activity of minocycline on various tumor cell lines in vitro].

作者信息

Inaba M, Nagashima K

出版信息

Gan To Kagaku Ryoho. 1986 Jul;13(7):2337-41.

PMID:3729489
Abstract

In order to investigate the possible mechanism for the therapeutic efficacy of tetracycline antibiotics against malignant pleural effusion, the effect of minocycline (MC), one of this type of antibiotic, on in vitro growth of tumor cells was examined. As a result, it was found that MC caused complete growth inhibition of various tumor cell lines at concentration of 10-20 micrograms/ml, but this action was reversible, suggesting that considerably long exposure time would be needed for these drugs to kill the tumor cells in vivo at a relatively low concentration. On the other hand, when a relatively high concentration of 100 micrograms/ml was applied, MC induced irreversible inhibition of cell growth even if the exposure time was comparatively short. Since 4 human lung tumor cell lines examined exhibited high sensitivity to these antibiotics, it seems possible that their direct administration in the form of a high-concentration solution into the pleural cavity would result in a direct cytostatic effect on tumor cells in clinical therapy.

摘要

为了探究四环素类抗生素治疗恶性胸腔积液的可能机制,研究了该类抗生素之一米诺环素(MC)对肿瘤细胞体外生长的影响。结果发现,MC在浓度为10 - 20微克/毫升时可导致各种肿瘤细胞系完全生长抑制,但这种作用是可逆的,这表明在体内以相对低浓度使用这些药物杀死肿瘤细胞需要相当长的暴露时间。另一方面,当应用100微克/毫升的相对高浓度时,即使暴露时间相对较短,MC也会诱导细胞生长的不可逆抑制。由于所检测的4种人肺肿瘤细胞系对这些抗生素表现出高敏感性,因此在临床治疗中以高浓度溶液形式直接注入胸腔似乎可能对肿瘤细胞产生直接的细胞抑制作用。

相似文献

1
[Growth-inhibitory activity of minocycline on various tumor cell lines in vitro].[米诺环素对多种肿瘤细胞系的体外生长抑制活性]
Gan To Kagaku Ryoho. 1986 Jul;13(7):2337-41.
2
In vivo antitumor activity of 4-amino 4-methyl 2-pentyne 1-al, an inhibitor of aldehyde dehydrogenase.醛脱氢酶抑制剂4-氨基-4-甲基-2-戊炔-1-醛的体内抗肿瘤活性
In Vivo. 1989 Sep-Oct;3(5):325-30.
3
[Antitumor effect of 1,3,3,5,5-pentaziridino-1-thia-2,4,6-triaza-3,5- diphoshorine-1-oxide].[1,3,3,5,5-五氮杂环丁烷-1-硫代-2,4,6-三氮杂-3,5-二磷杂环庚烷-1-氧化物的抗肿瘤作用]
Gan To Kagaku Ryoho. 1986 Dec;13(12):3401-7.
4
Comparison of antitumor effect of recombinant L-asparaginase with wild type one in vitro and in vivo.
Acta Pharmacol Sin. 2002 Oct;23(10):946-51.
5
Mechanism of antitumor action of pyrimidinones in the treatment of B16 melanoma and P388 leukemia.嘧啶酮类化合物治疗B16黑色素瘤和P388白血病的抗肿瘤作用机制
Cancer Res. 1985 Feb;45(2):532-8.
6
[Cytometric study of the effects of destruxin E on leukemic cells in mice].
C R Acad Sci III. 1987;305(14):575-8.
7
(R,R)-2,2'-[1,2-ethanediylbis[imino(1-methyl-2,1-ethanediyl)]]- bis[5-nitro-1H-benz[de]isoquinoline-1,3-(2H)-dione] dimethanesulfonate (DMP 840), a novel bis-naphthalimide with potent nonselective tumoricidal activity in vitro.(R,R)-2,2'-[1,2-乙二基双[亚氨基(1-甲基-2,1-乙二基)]]-双[5-硝基-1H-苯并[de]异喹啉-1,3-(2H)-二酮]二甲磺酸盐(DMP 840),一种新型双萘酰亚胺,在体外具有强大的非选择性杀肿瘤活性。
Cancer Res. 1994 Apr 15;54(8):2199-206.
8
Establishment of a group of murine leukemic cell lines and investigation of their biological characteristics.一组小鼠白血病细胞系的建立及其生物学特性研究。
Sci China B. 1989 Sep;32(9):1087-98.
9
Restoration of sensitivity to oxazaphosphorines by inhibitors of aldehyde dehydrogenase activity in cultured oxazaphosphorine-resistant L1210 and cross-linking agent-resistant P388 cell lines.在培养的对恶唑磷耐药的L1210细胞系和对交联剂耐药的P388细胞系中,通过醛脱氢酶活性抑制剂恢复对恶唑磷的敏感性。
Cancer Res. 1985 Apr;45(4):1549-55.
10
Effects of ellipticine on cell survival and cell cycle progression in cultured mammalian cells.玫瑰树碱对培养的哺乳动物细胞存活及细胞周期进程的影响。
Cancer Res. 1980 Jul;40(7):2390-9.