首页> 外文期刊>British Journal of Cancer >An Electron Microscope Study of Mitochondrial DNA in Spontaneous Human Tumours and Chemically Induced Animal Tumours
【24h】

An Electron Microscope Study of Mitochondrial DNA in Spontaneous Human Tumours and Chemically Induced Animal Tumours

机译:电子显微镜下自发性人类肿瘤和化学诱导的动物肿瘤中线粒体DNA的研究

获取原文
获取外文期刊封面目录资料

摘要

MtDNA was extracted by a phenol method from transplanted and primary DAB induced hepatomata in male Wistar rats, normal rat liver, spontaneous human tumours (2 Wilm's tumours, one neuroblastoma and one adrenal carcinoma), as well as 2 specimens of normal human kidney, BNU induced “leukaemias” in mice and CHO fibroblasts in monolayer culture. The proportion of monomers, catenated dimers and oligomers, open dimers and small circles was determined by electron microscopy of the fractions comprising lower and middle DNA bands in a CsCl-EthBr gradient. Tumours were compared where possible with their normal tissue of origin. Open dimers were found in 2 Wilm's tumours and their attached “normal-looking” kidney tissue but not in normal, non-malignant kidney or any other tissue studied. In Wilm's tumours, the occurrence of open dimers is far from being an all-or-none phenomenon. Malignancy produced little change in the relative proportions of catenated dimers and oligomers in the tissues studied. Small circles were found associated with mtDNA from every tissue. Tumour mtDNA was not more heterogeneous in length than monomers from the corresponding normal tissue, neither was the mean length of tumour mtDNA significantly different from its corresponding normal mtDNA.
机译:用苯酚法从雄性Wistar大鼠,正常大鼠肝脏,自发性人类肿瘤(2个威尔姆氏肿瘤,1个神经母细胞瘤和1个肾上腺癌)以及正常人肾脏,BNU的2个标本中移植的DAB引起的原发性肝肿中提取MtDNA。在单层培养中在小鼠和CHO成纤维细胞中诱导“白血病”。通过电子显微镜检查CsCl-EthBr梯度中包含较低和中等DNA条带的级分的单体,链状二聚体和寡聚体,开放二聚体和小圆圈的比例。将肿瘤与正常来源的组织进行比较。在2个Wilm肿瘤及其附着的“外观正常”的肾脏组织中发现开放的二聚体,但在正常,非恶性肾脏或任何其他研究的组织中未发现。在威尔姆肿瘤中,开放二聚体的出现远非全有或全无。恶性肿瘤在所研究的组织中的链状二聚体和寡聚体的相对比例几乎没有变化。发现每个组织中都有与mtDNA相关的小圆圈。肿瘤mtDNA的长度不比来自相应正常组织的单体的长度异质,肿瘤mtDNA的平均长度也没有与其对应的正常mtDNA明显不同。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号