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肾癌组织中线粒体融合蛋白2基因的表达及临床意义 被引量:2

Expression and clinical significance of Mitofusion 2 mRNA in renal cell carcinoma
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摘要 目的检测肾细胞癌线粒体融合蛋白-2(Mfn2)基因表达的变化,探讨其相关的临床意义。方法选取我院2014年2月至2016年1月收治的肾细胞癌患者74例,另取同期我院肾小球活检排除肾癌者30例作为对照组。Mfn2基因表达量使用荧光定量PCR检测。结果 Mfn2在肾癌组织中表达量为0.182±0.031,显著低于对照肾组织的0.325±0.047(P<0.01)。肾癌组织中男女性别、不同年龄以及肿瘤病理类型之间Mfn2表达量无显著性差异(P>0.05)。Ⅲ、Ⅳ临床分期患者Mfn2表达量为0.146±0.029,显著低于Ⅰ、Ⅱ临床分期患者的0.212±0.038(P<0.05)。肿瘤有淋巴结转移患者Mfn2表达量为0.151±0.024,显著低于无淋巴结转移患者的0.228±0.042(P<0.05)。肿瘤中、低分化患者Mfn2表达量为0.154±0.028,显著低于高分化患者的0.231±0.051(P<0.05)。结论 Mfn2基因在肾癌组织中低表达,Mfn2基因表达量与肾癌的临床分期、有无淋巴结转移以及肿瘤分化程度密切相关。 Objective To detect mitofusion 2 (Mfn2) mRNA expression in renal cell carcinoma (RCC) and to explore its clinical significance. Methods A total of 74 RCC cases and another 30 non-RCC controls were enrolled in this study. Realtime PCR was used to detect Mfn2 mRNA expression. Results Mfn2 mRNA expression was 0. 182±0. 031 vs. 0. 325±0. 047 in RCC cases and controls (P〈0.01). There were no statistical differences in Mfn2 mRNA expression between RCC patients of different gender, age, and pathological type (P〉0.05). Mfn2 mRNAexpression was 0. 146±0. 029 in Ⅲ and Ⅳ stage and 0.212 ± 0. 038 in Ⅰ and Ⅱ stage (P〈0.05). Mfn2 mRNA expression was 0.151± 0. 024 vs. 0.. 228 ± 0. 042 in lymph node metas- tasis group and non-lymph node metastasis group (P〈0.05). Mfn2 mRNA expression was 0. 154±0. 028 vs. 0. 231±0. 051 in median and low differentiation group, and well differentiation group (P〈0.05). ConclusionLow expression of Mfn2 mR- NA was detected in RCC, which was closely related to clinical stage, lymph node metastasis, and tumor differentiation.
出处 《现代泌尿外科杂志》 CAS 2016年第9期673-675,共3页 Journal of Modern Urology
关键词 肾癌 线粒体融合蛋白-2基因 荧光定量PCR renal cell carcinoma Mfn2 mRNA real-time PCR
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  • 1王萍,毋丽娜,蒋春笋,李志新,张颖妹,陈光慧,邱晓彦.人增殖抑制基因(HSG)对肿瘤细胞系化疗敏感性的作用[J].北京大学学报(医学版),2005,37(2):117-120. 被引量:15
  • 2叶章群,曾晓勇.当前膀胱癌研究热点与争论[J].临床外科杂志,2009,17(11). 被引量:5
  • 3夏耘,吴亚群,张林,李小兰,袁惠玲,何小军,陶德定,龚建平,裘法祖.线粒体融合素基因-2对人乳腺癌MCF-7细胞株增殖与化疗敏感性的影响[J].癌症,2007,26(8):815-819. 被引量:12
  • 4Karbowski M, Kurono C, Nishizawa Y, et al. Induction of megamitochondria by some chemicals inducing oxidative stress in primary cultured rat hepatocytes. Biochim Biophys Acta, 1997, 1349(3): 242-250.
  • 5Yu T, Robotham J L, Yoon Y. Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology. Proc Natl Aead Sci USA, 2006, 103(8): 2653-2658.
  • 6Chen G H, Liu N K, Zhou A, et al. The role of hypertension-related gene in aortic vascular smooth muscle cells from mice and rats. Chin Med J, 2001, 114(8): 833-836.
  • 7Karbowski M, Lee Y J, Gaume B, et al. Spatial and temporal association of Bax with mitochondrial fission sites, Drpl, and Mfn2 during apoptosis. J Cell Biol, 2002, 159(6): 931-938.
  • 8Ugioka R, Shimizu S, Tsujimoto Y. Fzol, aprotein involved in mitochondrial fusion, inhibits apoptosis. J Biol Chem, 2004, 279(50): 52726-52734.
  • 9Jahani A A, Cheung E C, Neuspiel M. Mitofusin 2 protects cerebellar granule neurons against injury induced cell death. J Biol Chem, 2007, 282(33): 23788-23798.
  • 10Guo X, Chen K H, Guo Y, et al. Mitofusin 2 triggers vascular smooth muscle cell apoptosis via mitochondrial death pathway. Circ Res, 2007, 101(11): 1113-1122.

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