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Quantitative detection of common deletion of mitochondrial DNA in hepatocellular carcinoma and hepatocellular nodular hyperplasia

机译:定量检测肝细胞癌和肝细胞结节性增生中线粒体DNA的常见缺失

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AIM: To study the deletion of mitochondiral DNA in hepatocellular carcinoma and hepatocellular nodular hyperplasia and its significance in the development of cancer. METHODS: Deleted mtDNA (CD-mtDNA) and wild type mtDNA (WT-mtDNA) were quantitatively analyzed by using real-time PCR in 27 hepatocellular carcinomas (HCC) and corresponding noncancerous liver tissues and 27 hepatocellular nodular hyperplasiae (HNH). RESULTS: A novel CD (4 981 bp) was detected in 85% (23/27) and 83%(22/27) of HCC and HNH tumor tissues, respectively, which were significantly higher than that in paired noncancerous liver tissues (57%, 15/27) (P<0.05). The CD/WT-mtDNA ratio in HCC tumors was 0.00092 (median, interquartile range, 0.0001202-0.00105), which was significantly higher than that in paired noncancerous liver tissues (median, 0.000, quartile range, 0-0) (P=0.002, Mann-Whitney Test), and was 25 of times of that in HNH tissues (median, 0.0000374, quartile range, 0-0.0004225) (P=0.002, Mann-Whitney test). CONCLUSION: CD-mtDNA mutation plays an important role in the development and progression of HCC.
机译:目的:研究肝细胞癌和肝细胞结节性增生中线粒体DNA的缺失及其在癌症发展中的意义。方法:采用实时荧光定量PCR技术对27例肝细胞癌(HCC)和相应的非癌性肝组织以及27例肝细胞结节性增生(HNH)中的缺失mtDNA(CD-mtDNA)和野生型mtDNA(WT-mtDNA)进行了定量分析。结果:在HCC和HNH肿瘤组织中分别检出85%(23/27)和83%(22/27)的CD(4 981 bp),显着高于配对的非癌肝组织(57)。 %,15/27)(P <0.05)。 HCC肿瘤的CD / WT-mtDNA比率为0.00092(中位数,四分位间距,0.0001202-0.00105),显着高于配对的非癌肝组织(中位数,0.000,四分位间距,0-0)(P = 0.002) (Mann-Whitney检验),是HNH组织中的25倍(中位数为0.0000374,四分位数范围为0-0.0004225)(P = 0.002,Mann-Whitney检验)。结论:CD-mtDNA突变在肝癌的发生发展中起重要作用。

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