期刊文献+

血浆miR-122表达与肝癌手术前后肝损伤的相关性 被引量:2

Correlation between Expression of Plasma miR-122 and Liver Injury before and after Liver Cancer Surgery
原文传递
导出
摘要 目的:探讨血浆中micro RNA-122(miR-122)表达与肝癌根治切除术前后肝损伤的相关性。方法:选取2015年1月-2016年1月在我院择期行肝癌根治切除术的肝癌患者36例,作为研究组,另选择同期健康体检者30例作为对照组。分别取研究组患者术前、术后第1 d、7 d及对照组入组时的清晨肘静脉血,采取荧光定量PCR(RT-PCR)技术检测血浆中miR-122表达水平,并检测两组血浆丙氨酸氨基转移酶(ALT)及转化生长因子-β1(TGF-β1)水平,分析手术前后研究组中各指标的相关性。结果:研究组术前血浆miR-122表达水平与血浆ALT、TGF-β1水平均高于对照组(P<0.05)。与术前比较,研究组术后1 d血浆miR-122表达水平与血浆ALT、TGF-β1水平均明显上升(P<0.05);且与术后1 d比较,肝癌患者术后7 d血浆miR-122、ALT、TGF-β1水平明显下降,且与术前比较差异有统计学意义(P<0.05)。肝癌患者术前、术后1 d、7 d血浆miR-122表达水平与血浆ALT、TGF-β1水平均呈正相关(均P<0.05)。结论:血浆miR-122与肝癌根治切除术前后肝功能损伤有关,可作为一种新型生物学指标。 Objective: To explore the correlation between expression of plasma micro RNA-122 (miR-122) and liver injury before and alter radical resection of liver cancer. Methods: Selected 36 patients who were underwent selective radical resection of liver cancer as the research group in our hospital from January 2015 to January 2016, in the same time selected 30 cases of healthy physical examination as the control group. Collected the early morning elbow vein blood of research group before operation and 1 d, 7 d after operation and the control group, the expression of plasma miR-122 in two groups were detected by Real-time PCR (RT-PCR) technique, and detected the levels of plasma alanine aminotransferase (ALT) and transforming growth factor-β1 (TGF-β1), then analyzed the correlation between above indexes in research group before and alter operation. Results: The expression of plasma miR-122, plasma ALT and TGF-β1 in the research group before operation were higher than that in the control group (P〈0.05); In research group, the expression of plasma miR-122, plasma ALT and TGF-β1 ld after operation were significantly increased compared with before operation (P〈0.05), but they were decreased 7 d alter operation compared with 1 d alter operation, which was statistically different from before operation(P〈0.05); The expression of plasma miR-122 in research group before operation and 1 d, 7 d alter operation were positively correlated with plasma ALT and TGF-β1 (P〈0.05). Conclusion: Plasma miR-122 is related to liver injury before and alter radical resection of liver cancer, which could be a new biological index.
出处 《现代生物医学进展》 CAS 2017年第14期2697-2699,2710,共4页 Progress in Modern Biomedicine
基金 全军医学科技青年培育项目(13QNP023)
关键词 肝癌 肝切除术 肝损伤 血浆miR-122 Liver cancer Hepatectomy Liver injury Plasma miR- 122
  • 相关文献

参考文献3

二级参考文献105

  • 1Huang, Fan,Geng, Xiao-Ping.Chemokines and hepatocellular carcinoma[J].World Journal of Gastroenterology,2010,16(15):1832-1836. 被引量:19
  • 2施国英,施德金,吕伟标,陈永坤,童向民.基质细胞衍化生长因子-1及其受体CXCR4在肝细胞癌和肝硬化中的表达[J].中华肝脏病杂志,2007,15(4):276-278. 被引量:12
  • 3Lee UE, Friedman SL. Mechanisms of hepatic fibrogenesis. BestPract Res Clin Gastroenterol 2011; 25: 195-206 [PMID: 21497738DOI: 10.1016/j.bpg.2011.02.005].
  • 4Mormone E, George J, Nieto N. Molecular pathogenesis ofhepatic fibrosis and current therapeutic approaches. Chem BiolInteract 2011; 193: 225-231 [PMID: 21803030 DOI: 10.1016/j.cbi.2011.07.001].
  • 5Chen SL, Zheng MH, Shi KQ, Yang T, Chen YP. A new strategyfor treatment of liver fibrosis: letting MicroRNAs do the job.BioDrugs 2013; 27: 25-34 [PMID: 23329398 DOI: 10.1007/s40259-012-0005-2].
  • 6Gressner OA, Weiskirchen R, Gressner AM. Biomarkers of liverfibrosis: clinical translation of molecular pathogenesis or basedon liver-dependent malfunction tests. Clin Chim Acta 2007; 381:107-113 [PMID: 17399697].
  • 7Bandyopadhyay S, Friedman RC, Marquez RT, Keck K, KongB, Icardi MS, Brown KE, Burge CB, Schmidt WN, Wang Y,McCaffrey AP. Hepatitis C virus infection and hepatic stellate cellactivation downregulate miR-29: miR-29 overexpression reduceshepatitis C viral abundance in culture. J Infect Dis 2011; 203:1753-1762 [PMID: 21606534 DOI: 10.1093/infdis/jir186].
  • 8Haybaeck J, Zeller N, Heikenwalder M. The parallel universe:microRNAs and their role in chronic hepatitis, liver tissue damageand hepatocarcinogenesis. Swiss Med Wkly 2011; 141: w13287[PMID: 22020555 DOI: 10.4414/smw.2011.13287].
  • 9He Y, Huang C, Zhang SP, Sun X, Long XR, Li J. The potentialof microRNAs in liver fibrosis. Cell Signal 2012; 24: 2268-2272[PMID: 22884954 DOI: 10.1016/j.cellsig.2012.07.023].
  • 10Noetel A, Kwiecinski M, Elfimova N, Huang J, Odenthal M.microRNA are Central Players in Anti- and Profibrotic GeneRegulation during Liver Fibrosis. Front Physiol 2012; 3: 49 [PMID:22457651 DOI: 10.3389/fphys.2012.00049].

共引文献15

同被引文献18

引证文献2

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部