文章摘要
曹海燕 翟玉龙 孙夏承 安家泽 吕英华 邢金良△ 黄启超.基于电镜和免疫组化的线粒体数目标志物评估肝癌的初步研究[J].,2016,16(14):2646-2650
基于电镜和免疫组化的线粒体数目标志物评估肝癌的初步研究
Evaluation of Hepatocellular Carcinoma Growth Based on MitochondrialMolecular Marker using Transmission Electron Microscope andImmunohistochemistry
  
DOI:
中文关键词: 线粒体定量  电子显微镜  COX IV  HSP60
英文关键词: Quantification of mitochondria  Transmission electron microscope  COX IV  HSP60
基金项目:国家自然科学基金项目(81572410;31401221)
作者单位
曹海燕 翟玉龙 孙夏承 安家泽 吕英华 邢金良△ 黄启超 第四军医大学基础医学教学实验中心第四军医大学唐都医院普通外科 第四军医大学西京医院肝胆外科 
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中文摘要:
      目的:研究线粒体数目与肝癌生长的相关性。方法:利用电子显微镜技术定量肝癌组织中线粒体数目,利用免疫组织化学技 术评估肝癌组织中的线粒体标志物COX IV 及HSP60 表达水平,分析电镜肝癌线粒体定量结果与COX IV 及HSP60 表达量之间 的相关性,并比较肝癌中线粒体数目、COX IV 及HSP60 表达量与肝癌直径之间的关系。结果:与癌旁相比,肝癌组织中线粒体数 目(P<0.001)、COX IV 及HSP60的表达量显著降低(P=0.0417,P=0.0290)。COX IV 及HSP60 表达水平与线粒体数目无显著相关 (r2=0.009,P=0.5468;r2=0.056,P=0.1396)。线粒体数目与肿瘤直径显著负相关(r2=0.1086,P=0.0434),COX IV 及HSP60表达量与 肿瘤直径无显著相关(r2=0.0251,P=0.3287;r2=0.0461,P=0.1830)。结论:线粒体数目是潜在的肝癌生长标志物。但常用的线粒体定 量分子HSP60 与COX IV 并不能准确定量肝癌线粒体。
英文摘要:
      Objective:To evaluate the correlation between mitochondrial number and tumor growth in Hepatocellular carcinoma (HCC).Methods:Transmission electron microscope was used to quantify the number of mitochondria in HCC tissues. Immunohistochemistry was used to evaluate the expression levels of COX IV and HSP60 in HCC tissues.Results:Mitochondrial number (P<0.001) and the expression levels of COX IV and HSP60 (P=0.0417, P=0.0290) were decreased in HCC tissues when compared to paired non-tumor tissues. Correlation analysis showed that mitochondrial number (r2=0.1086, P=0.0434), but not COX IV and HSP60 (r2=0.009, P=0.5468; r2=0.056, P=0.1396), was significantly negatively associated with tumor diameter. No significant correlation was found between the expression level of COX IV or HSP60 and mitochondrial number in HCC tissues (r2=0.0251, P=0.3287; r2=0.0461, P=0.1830).Conclusion:Mitochondrial number is a potential biomarker for evaluating tumor growth and prognosis of HCC. Whereas, the commonly used molecular markers COX IV and HSP60 are not suitable for quantification of mitochondria in HCC tissues.
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