• 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

硫酸镍和苯并[a]芘对仓鼠胚胎细胞形态转化的协同作用。

Synergistic effect on morphological transformation of hamster embryo cells by nickel sulphate and benz[a]pyrene.

作者信息

Rivedal E, Sanner T

出版信息

Cancer Lett. 1980 Jan;8(3):203-8. doi: 10.1016/0304-3835(80)90002-6.

DOI:10.1016/0304-3835(80)90002-6
PMID:7226142
Abstract

Morphological transformation and induction of somatic mutation in the hamster embryo cell bioassay have been used to study whether the carcinogenicity of nickel is affected by polycyclic hydrocarbons. The transformation frequency was found to increase with increasing concentration of nickel sulphate, benz[a]pyrene (BP) and methylcholanthrene. In experiments with combinations of nickel sulphate and BP, the transformation frequencies used for all concentrations were higher than for compounds tested separately. The greatest enhancement was found using 5 micrograms/ml NiSO4 . 6H2O and 0.78 microgram/ml BP. The transformation frequency obtained with this combination was 10.7%, compared to 0.5% and 0.6% for the individual substances. No synergistic effect could be detected between nickel sulphate and methylcholanthrene (MC). In experiments measuring somatic mutation by selection for ouabain resistance, the mutation frequency was likewise found to be significantly higher than expected in mixtures of nickel sulphate and BP. The present demonstration of the synergistic effect between nickel sulphate and BP is of interest with the potentiating effect of cigarette smoking on development of lung cancer among nickel refinery workers.

摘要

在仓鼠胚胎细胞生物测定中,利用形态学转化和体细胞突变诱导来研究镍的致癌性是否受多环烃影响。发现转化频率随硫酸镍、苯并[a]芘(BP)和甲基胆蒽浓度的增加而升高。在硫酸镍和BP组合的实验中,所有浓度下的转化频率均高于单独测试的化合物。使用5微克/毫升硫酸镍·6水合物和0.78微克/毫升BP时增强作用最大。该组合获得的转化频率为10.7%,而单个物质分别为0.5%和0.6%。在硫酸镍和甲基胆蒽(MC)之间未检测到协同效应。在通过选择哇巴因抗性来测量体细胞突变的实验中,同样发现硫酸镍和BP混合物中的突变频率显著高于预期。硫酸镍和BP之间协同效应的当前证明对于吸烟对镍精炼厂工人肺癌发生的增强作用具有重要意义。

相似文献

1
Synergistic effect on morphological transformation of hamster embryo cells by nickel sulphate and benz[a]pyrene.硫酸镍和苯并[a]芘对仓鼠胚胎细胞形态转化的协同作用。
Cancer Lett. 1980 Jan;8(3):203-8. doi: 10.1016/0304-3835(80)90002-6.
2
Synergistic effects of cigarette smoke extracts, benz (a) pyrene and nickel sulphate on morphological transformation of hamster embryo cells.香烟烟雾提取物、苯并(a)芘和硫酸镍对仓鼠胚胎细胞形态转化的协同作用。
Dev Toxicol Environ Sci. 1980;8:259-63.
3
Potentiating effect of cigarette smoke extract on morphological transformation of hamster embryo cells by benzo[alpha]pyrene.香烟烟雾提取物对苯并[a]芘诱导的仓鼠胚胎细胞形态转化的增强作用。
Cancer Lett. 1980 Sep;10(3):193-8. doi: 10.1016/0304-3835(80)90071-3.
4
Metal salts as promoters of in vitro morphological transformation of hamster embryo cells initiated by benzo(a)pyrene.金属盐作为苯并(a)芘引发的仓鼠胚胎细胞体外形态转化的促进剂。
Cancer Res. 1981 Jul;41(7):2950-3.
5
Evaluation of tumour promoters by the hamster embryo cell transformation assay.通过仓鼠胚胎细胞转化试验评估肿瘤启动子。
IARC Sci Publ. 1982(39):251-8.
6
Asbestos and benzo(a)pyrene synergism in the transformation of Syrian hamster embryo cells.
Pharmacology. 1983;27(2):65-73. doi: 10.1159/000137837.
7
Enhancement of adenovirus transformation by pretreatment of hamster cells with carcinogenic polycyclic hydrocarbons.用致癌多环烃预处理仓鼠细胞增强腺病毒转化作用。
Cancer Res. 1973 Apr;33(4):819-24.
8
Transformation of hamster cells in vitro by polycyclic hydrocarbons without cytotoxicity.多环烃在无细胞毒性情况下对仓鼠细胞的体外转化
Proc Natl Acad Sci U S A. 1971 Dec;68(12):2958-61. doi: 10.1073/pnas.68.12.2958.
9
Morphologic and neoplastic transformation of Syrian hamster embryo fibroblasts by diethylstilbestrol and its analogs.己烯雌酚及其类似物对叙利亚仓鼠胚胎成纤维细胞的形态学和肿瘤性转化作用
Cancer Res. 1982 Aug;42(8):3040-5.
10
Promotional effect of different phorbol esters on morphological transformation of hamster embryo cells.不同佛波酯对仓鼠胚胎细胞形态转化的促进作用。
Cancer Lett. 1982 Oct;17(1):1-8. doi: 10.1016/0304-3835(82)90101-x.

引用本文的文献

1
In vitro assessment of the toxicity of metal compounds : I. Mammalian Cell transformation.金属化合物的体外毒性评估:I. 哺乳动物细胞转化。
Biol Trace Elem Res. 1982 Jun;4(2-3):71-82. doi: 10.1007/BF02783248.
2
Genetic and epigenetic mechanisms in metal carcinogenesis and cocarcinogenesis: nickel, arsenic, and chromium.金属致癌和促癌过程中的遗传和表观遗传机制:镍、砷和铬
Chem Res Toxicol. 2008 Jan;21(1):28-44. doi: 10.1021/tx700198a. Epub 2007 Oct 30.
3
Current aspects in metal genotoxicity.金属遗传毒性的当前研究方向。
Biometals. 1995 Jan;8(1):3-11. doi: 10.1007/BF00156151.
4
Carcinogenic nickel silences gene expression by chromatin condensation and DNA methylation: a new model for epigenetic carcinogens.致癌性镍通过染色质浓缩和DNA甲基化使基因表达沉默:一种表观遗传致癌物的新模型。
Mol Cell Biol. 1995 May;15(5):2547-57. doi: 10.1128/MCB.15.5.2547.
5
Recent research on nickel carcinogenesis.近期关于镍致癌作用的研究。
Environ Health Perspect. 1981 Aug;40:131-41. doi: 10.1289/ehp.8140131.
6
Role of metals in carcinogenesis. Problems of epidemiological evidence.金属在致癌过程中的作用。流行病学证据问题。
Environ Health Perspect. 1981 Aug;40:11-20. doi: 10.1289/ehp.40-1568824.
7
Erythropoietin-mediated erythrocytosis in rodents after intrarenal injection of nickel subsulfide.肾内注射硫化镍后啮齿动物中促红细胞生成素介导的红细胞增多症。
Yale J Biol Med. 1982 Mar-Apr;55(2):123-36.
8
Effects of toxic chemicals on the release of pyrimidine compounds in cell culture.
Arch Toxicol. 1987 Jul;60(5):388-93. doi: 10.1007/BF00295760.
9
Superoxide dismutase activity and novel reactions with hydrogen peroxide of histidine-containing nickel(II)-oligopeptide complexes and nickel(II)-induced structural changes in synthetic DNA.含组氨酸的镍(II)-寡肽配合物的超氧化物歧化酶活性及与过氧化氢的新反应,以及镍(II)诱导的合成DNA结构变化
Biol Trace Elem Res. 1989 Jul-Sep;21:23-33. doi: 10.1007/BF02917233.
10
Morphological transformation and catalase activity of Syrian hamster embryo cells treated with hepatic peroxisome proliferators, TPA and nickel sulphate.用肝过氧化物酶体增殖剂、佛波酯和硫酸镍处理的叙利亚仓鼠胚胎细胞的形态转化和过氧化氢酶活性
Cell Biol Toxicol. 1990 Jan;6(1):1-13. doi: 10.1007/BF00135022.