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2016 | 63 | 3 | 527-531

Article title

Hepatic expression of miR-122 and antioxidant genes in patients with chronic hepatitis B

Content

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Languages of publication

EN

Abstracts

EN
Introduction: The pathogenesis of chronic hepatitis B depends on both, the immune response and oxidative stress. Aim of the study: To assess the hepatic expression of miR-122 and the antioxidant genes: HMOX-1, NQO1 and GFER1, in liver biopsy specimens obtained from patients with chronic hepatitis B, with regard to selected clinical and histological parameters, using RT-PCR. Results: The study group comprised 34 HBV-infected patients. Statistically significant associations were found between lower hepatic expression of HMOX-1 and greater severity of liver inflammation (p=0.04). However, significantly higher expression of NQO1 was observed in patients with advanced liver fibrosis (p=0.035). Hepatic expression of miR-122 in HBV patients was not associated with viral load or liver injury. Conclusion: The hepatic expression of HMOX-1and NQO1 may be associated with liver injuries in chronic hepatitis B. However, hepatic expression of miR-122 does not seem to correspond to progression of the liver disease.

Keywords

Year

Volume

63

Issue

3

Pages

527-531

Physical description

Dates

published
2016
received
2015-11-24
revised
2016-04-20
accepted
2016-05-18
(unknown)
2016-07-08

Contributors

  • Department of Infectious Diseases and Hepatology, Medical University of Lodz, Łódź, Poland
  • Department of Infectious Diseases and Hepatology, Medical University of Lodz, Łódź, Poland
  • Central Laboratory, Medical University of Lodz, Łódź, Poland
  • Department of Infectious Diseases and Hepatology, Medical University of Lodz, Łódź, Poland

References

  • Chen G, Lin W, Shen F, Iloeje UH, London WT, Evans AA (2006) Past HBV viral load as predictor of mortality and morbidity from HCC and chronic liver disease in a prospective study. Am J Gastroenterol 101: 1797-1803.
  • Cheng ML, Lu YF, Chen H, Shen ZY, Liu J (2015) Liver expression of Nrf2-related genes in different liver diseases. Hepatobiliary Pancreat Dis Int 14: 485-491.
  • Chisari FV, Isogawa M, Wieland SF (2010) Pathogenesis of hepatitis B virus infection. Pathol Biol (Paris) 58: 258-266. doi: 10.1016/j.patbio.2009.11.001.
  • Guidotti LG, Chisari FV (2006) Immunobiology and pathogenesis of viral hepatitis. Annu Rev Pathol 1: 23-61.
  • Iloeje UH, Yang HI, Su J, Jen CL, You SL, Chen CJ; Risk Evaluation of Viral Load Elevation and Associated Liver Disease/Cancer-In HBV (the REVEAL-HBV) Study Group (2006) Predicting cirrhosis risk based on the level of circulating hepatitis B viral load. Gastroenterology 130: 678-686.
  • Li Q, Liu DM, Zhang LM, Zhu B, He YT, Xiao YH (2005) Effects of augmentation of liver regeneration recombinant plasmid on rat hepatic fibrosis. World J Gastroenterol 11: 2438-2443.
  • Maines MD (1997) The heme oxygenase system: a regulator of second messenger gases. Annu Rev Pharmacol Toxicol 37: 517-554.
  • Qiu L, Fan H, Jin W, Zhao B, Wang Y, Ju Y, Chen L, Chen Y, Duan Z, Meng S (2010) miR-122-induced down-regulation of HO-1 negatively affects miR-122-mediated suppression of HBV. Biochem Biophys Res Commun 398: 771-777. doi: 10.1016/j.bbrc.2010.07.021.
  • Protzer U, Seyfried S, Quasdorff M, Sass G, Svorcova M, Webb D, Bohne F, Hösel M, Schirmacher P, Tiegs G (2007) Antiviral activity and hepatoprotection by heme oxygenase-1 in hepatitis B virus infection. Gastroenterology 133: 1156-1165.
  • Roderburg C, Urban GW, Bettermann K, Vucur M, Zimmermann H, Schmidt S, Janssen J, Koppe C, Knolle P, Castoldi M, Tacke F, Trautwein C, Luedde T (2011) Micro-RNA profiling reveals a role for miR-29 in human and murine liver fibrosis. Hepatology 53: 209-218. doi: 10.1002/hep.23922.
  • Siegel D, Ross D (2000) Immunodetection of NAD(P)H:quinone oxidoreductase 1 (NQO1) in human tissues. Free Radic Biol Med 29: 246-253.
  • Tanigawa K, Sakaida I, Masuhara M, Hagiya M, Okita K (2000) Augmenter of liver regeneration (ALR) may promote liver regeneration by reducing natural killer (NK) cell activity in human liver diseases. J Gastroenterol 35: 112-119.
  • Tasdelen Fisgin N, Aydin BK, Sarikaya H, Tanyel E, Esen S, Sunbul M, Leblebicioglu H (2012) Oxidative stress and antioxidant defense in patients with chronic hepatitis B. Clin Lab 58: 273-280.
  • Wang S, Qiu L, Yan X, Jin W, Wang Y, Chen L, Wu E, Ye X, Gao GF, Wang F, Chen Y, Duan Z, Meng S (2012) Loss of microRNA 122 expression in patients with hepatitis B enhances hepatitis B virus replication through cyclin G(1)-modulated P53 activity. Hepatology 55: 730-741. doi: 10.1002/hep.24809.
  • Waris G, Huh KW, Siddiqui A (2001) Mitochondrially associated hepatitis B virus X protein constitutively activates transcription factors STAT-3 and NF-kappa B via oxidative stress. Mol Cell Biol 21: 7721-7730.
  • World Health Organization (2000) Hepatitis B.
  • Wunder C, Potter RF (2003) The heme oxygenase system: its role in liver inflammation. Curr Drug Targets Cardiovasc Haematol Disord 3: 199-208.
  • Xing TJ, Jiang DF, Huang JX, Xu ZL (2014) Expression and clinical significance of miR-122 and miR-29 in hepatitis B virus-related liver disease. Genet Mol Res 13: 7912-7918. doi: 10.4238/2014.
  • Zhang H, Li QY, Guo ZZ, Guan Y, Du J, Lu YY, Hu YY, Liu P, Huang S, Su SB (2012) Serum levels of microRNAs can specifically predict liver injury of chronic hepatitis B. World J Gastroenterol 18: 5188-5196. doi: 10.3748/wjg.v18.i37.5188.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv63p527kz
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