Expression of Biliverdin Reductase A in peripheral blood leukocytes is associated with treatment response in HCV-infected patients
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23536765
PubMed Central
PMC3594226
DOI
10.1371/journal.pone.0057555
PII: PONE-D-12-10958
Knihovny.cz E-zdroje
- MeSH
- antivirové látky terapeutické užití MeSH
- dospělí MeSH
- exprese genu * MeSH
- hem metabolismus MeSH
- hemová oxygenasa (decyklizující) genetika metabolismus MeSH
- hemoxygenasa-1 genetika metabolismus MeSH
- Hepacivirus * MeSH
- hepatitida C farmakoterapie genetika virologie MeSH
- játra metabolismus virologie MeSH
- leukocyty metabolismus virologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- metabolické sítě a dráhy genetika MeSH
- oxidoreduktasy působící na CH-CH vazby genetika MeSH
- ROC křivka MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antivirové látky MeSH
- biliverdin reductase MeSH Prohlížeč
- hem MeSH
- heme oxygenase-2 MeSH Prohlížeč
- hemová oxygenasa (decyklizující) MeSH
- hemoxygenasa-1 MeSH
- oxidoreduktasy působící na CH-CH vazby MeSH
BACKGROUND AND AIMS: Hepatitis C virus (HCV) infection is associated with systemic oxidative stress. Since the heme catabolic pathway plays an important role in antioxidant protection, we attempted to assess the gene expression of key enzymes of heme catabolism, heme oxygenase 1 (HMOX1), heme oxygenase 2 (HMOX2), and biliverdin reductase A (BLVRA) in the liver and peripheral blood leukocytes (PBL) of patients chronically infected with HCV. METHODS: Gene expressions (HMOX1, HMOX2, BLVRA) and HCV RNA were analyzed in PBL of HCV treatment naïve patients (n = 58) and controls (n = 55), with a subset of HCV patients having data on hepatic gene expression (n = 35). Based upon the therapeutic outcome, HCV patients were classified as either responders (n = 38) or treatment-failure patients (n = 20). Blood samples in HCV patients were collected at day 0, and week 12, 24, 36, and 48 after the initiation of standard antiviral therapy. RESULTS: Compared to the controls, substantially increased BLVRA expression was detected in PBL (p<0.001) of therapeutically naïve HCV patients. mRNA levels of BLVRA in PBL closely correlated with those in liver tissue (r2 = 0.347,p = 0.03). A marked difference in BLVRA expression in PBL between the sustained responders and patients with treatment failure was detected at week 0 and during the follow-up (p<0.001). Multivariate analysis revealed that BLVRA basal expression in PBL was an independent predictor for sustained virological response (OR 15; 95% CI 1.05-214.2; P = 0.046). HMOX1/2 expression did not have any effect on the treatment outcome. CONCLUSION: Our results suggest that patients with chronic HCV infection significantly upregulate BLVRA expression in PBL. The lack of BLVRA overexpression is associated with non-responsiveness to standard antiviral therapy; whereas, HMOX1/2 does not seem to have any predictive potential.
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Seeff LB (1997) Natural history of hepatitis C. Hepatology. 26: 21S–28S. PubMed
World Health Organization: Hepatitis C. World Health Organization Fact sheet 164 (Revised June 2011). Available: http://www.who.int/mediacentre/factsheets/fs164/en/. Accessed 2012 Feb 4.
Nemecek V, Castkova J, Fritz P, Linhartova A, Svandova E, et al. (2003) The 2001 serological survey in the Czech Republic-viral hepatitis. Cent Eur J Public Health 11 Suppl: S54–61 PubMed
Nemecek V, Strunecky O (2009) Genotypic heterogeneity of hepatitis C virus (HCV) from blood donors in the Czech Republic. Epidemiol Mikrobiol Imunol 58: 63–72. PubMed
Wang JT, Sheu JC, Lin JT, Wang TH, Chen DS (1992) Detection of replicative form of hepatitis C virus RNA in peripheral blood mononuclear cells. J Infect Dis 166: 1167–1169. PubMed
Peterhans E (1997) Reactive oxygen species and nitric oxide in viral diseases. Biol Trace Elem Res 56: 107–116. PubMed
Okuda M, Li K, Beard MR, Showalter LA, Scholle F, et al. (2002) Mitochondrial injury, oxidative stress, and antioxidant gene expression are induced by hepatitis C virus core protein. Gastroenterology 122: 366–375. PubMed
Abdalla MY, Britigan BE, Wen F, Icardi M, McCormick ML, et al. (2004) Down-regulation of heme oxygenase-1 by hepatitis C virus infection in vivo and by the in vitro expression of hepatitis C core protein. J Infect Dis 190: 1109–1118. PubMed
Sass G, Seyfried S, M PS, Yamashita K, Kaczmarek E, et al. (2004) Cooperative effect of biliverdin and carbon monoxide on survival of mice in immune-mediated liver injury. Hepatology 40: 1128–1135. PubMed
Verma A, Hirsch DJ, Glatt CE, Ronnett GV, Snyder SH (1993) Carbon monoxide: a putative neural messenger. Science 259: 381–384. PubMed
Vitek L, Schwertner HA (2007) The heme catabolic pathway and its protective effects on oxidative stress-mediated diseases. Adv Clin Chem 43: 1–57. PubMed
Maines MD, Panahian N (2001) The heme oxygenase system and cellular defense mechanisms. Do HO-1 and HO-2 have different functions? Adv Exp Med Biol 502: 249–272. PubMed
Willis D, Moore AR, Frederick R, Willoughby DA (1996) Heme oxygenase: a novel target for the modulation of the inflammatory response. Nat Med 2: 87–90. PubMed
Li L, Grenard P, Nhieu JT, Julien B, Mallat A, et al. (2003) Heme oxygenase-1 is an antifibrogenic protein in human hepatic myofibroblasts. Gastroenterology 125: 460–469. PubMed
Sass G, Soares MC, Yamashita K, Seyfried S, Zimmermann WH, et al. (2003) Heme oxygenase-1 and its reaction product, carbon monoxide, prevent inflammation-related apoptotic liver damage in mice. Hepatology 38: 909–918. PubMed
Zhu Z, Wilson AT, Mathahs MM, Wen F, Brown KE, et al. (2008) Heme oxygenase-1 suppresses hepatitis C virus replication and increases resistance of hepatocytes to oxidant injury. Hepatology 48: 1430–1439. PubMed PMC
Ghaziani T, Shan Y, Lambrecht RW, Donohue SE, Pietschmann T, et al. (2006) HCV proteins increase expression of heme oxygenase-1 (HO-1) and decrease expression of Bach1 in human hepatoma cells. J Hepatol 45: 5–12. PubMed
Baranano DE, Rao M, Ferris CD, Snyder SH (2002) Biliverdin reductase: a major physiologic cytoprotectant. Proc Natl Acad Sci U S A 99: 16093–16098. PubMed PMC
Miralem T, Hu Z, Torno MD, Lelli KM, Maines MD (2005) Small interference RNA-mediated gene silencing of human biliverdin reductase, but not that of heme oxygenase-1, attenuates arsenite-mediated induction of the oxygenase and increases apoptosis in 293A kidney cells. J Biol Chem 280: 17084–17092. PubMed
Florczyk UM, Jozkowicz A, Dulak J (2008) Biliverdin reductase: new features of an old enzyme and its potential therapeutic significance. Pharmacol Rep 60: 38–48. PubMed PMC
Ahmad Z, Salim M, Maines MD (2002) Human biliverdin reductase is a leucine zipper-like DNA-binding protein and functions in transcriptional activation of heme oxygenase-1 by oxidative stress. J Biol Chem 277: 9226–9232. PubMed
Kravets A, Hu Z, Miralem T, Torno MD, Maines MD (2004) Biliverdin reductase, a novel regulator for induction of activating transcription factor-2 and heme oxygenase-1. J Biol Chem 279: 19916–19923. PubMed
Ding B, Gibbs PE, Brookes PS, Maines MD (2011) The coordinated increased expression of biliverdin reductase and heme oxygenase-2 promotes cardiomyocyte survival: a reductase-based peptide counters beta-adrenergic receptor ligand-mediated cardiac dysfunction. FASEB J 25: 301–313. PubMed PMC
Yamaguchi T, Komoda Y, Nakajima H (1994) Biliverdin-IX alpha reductase and biliverdin-IX beta reductase from human liver. Purification and characterization. J Biol Chem 269: 24343–24348. PubMed
Maines MD (2010) Potential application of biliverdin reductase and its fragments to modulate insulin/IGF-1/MAPK/PI3-K signaling pathways in therapeutic settings. Curr Drug Targets 11: 1586–1594. PubMed
Lehmann E, El-Tantawy WH, Ocker M, Bartenschlager R, Lohmann V, et al. (2010) The heme oxygenase 1 product biliverdin interferes with hepatitis C virus replication by increasing antiviral interferon response. Hepatology 51: 398–404. PubMed
Huang C, Chen H, Cassidy W, Howell CD (2008) Peripheral blood gene expression profile associated with sustained virologic response after peginterferon plus ribavirin therapy for chronic hepatitis-C genotype 1. J Natl Med Assoc 100: 1425–1433. PubMed
Ghany MG, Strader DB, Thomas DL, Seeff LB (2009) Diagnosis, management, and treatment of hepatitis C: an update. Hepatology 49: 1335–1374. PubMed PMC
Ishak K, Baptista A, Bianchi L, Callea F, De Groote J, et al. (1995) Histological grading and staging of chronic hepatitis. J Hepatol 22: 696–699. PubMed
Carriere M, Pene V, Breiman A, Conti F, Chouzenoux S, et al. (2007) A novel, sensitive, and specific RT-PCR technique for quantitation of hepatitis C virus replication. J Med Virol 79: 155–160. PubMed
Vreman HJ, Stevenson DK (1988) Detection of heme oxygenase activity by measurement of CO. In: Maines MD, Costa LG, Reed DJ, Sassa S, Sipes IG. Current Protocols in Toxicology. New York: John Wiley&Sons. 9.2.1–9.2.10. PubMed
Zhu Z, Wilson AT, Luxon BA, Brown KE, Mathahs MM, et al. (2010) Biliverdin inhibits hepatitis C virus nonstructural 3/4A protease activity: mechanism for the antiviral effects of heme oxygenase? Hepatology 52: 1897–1905. PubMed PMC
Wen F, Brown KE, Britigan BE, Schmidt WN (2008) Hepatitis C core protein inhibits induction of heme oxygenase-1 and sensitizes hepatocytes to cytotoxicity. Cell Biol Toxicol 24: 175–188. PubMed
Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, et al. (2009) Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. Nature 461: 399–401. PubMed
Suppiah V, Moldovan M, Ahlenstiel G, Berg T, Weltman M, et al. (2009) IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. Nat Genet 41: 1100–1104. PubMed
Thompson AJ, Muir AJ, Sulkowski MS, Ge D, Fellay J, et al. (2010) Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus. Gastroenterology 139: 120–129. PubMed
Frankova S, Bartakova R, Hejda V, Urbanek P, Husova L, et al. (2012) IL28 rs 12979860 CC genotype slows progression of liver disease in HCV infected patients. Gastroenterologie a Hepatologie 66: S17.
Lanford RE, Guerra B, Lee H, Chavez D, Brasky KM, et al. (2006) Genomic response to interferon-alpha in chimpanzees: implications of rapid downregulation for hepatitis C kinetics. Hepatology 43: 961–972. PubMed
Waddell SJ, Popper SJ, Rubins KH, Griffiths MJ, Brown PO, et al. (2010) Dissecting interferon-induced transcriptional programs in human peripheral blood cells. PLoS One 5: e9753. PubMed PMC
He XS, Ji X, Hale MB, Cheung R, Ahmed A, et al. (2006) Global transcriptional response to interferon is a determinant of HCV treatment outcome and is modified by race. Hepatology 44: 352–359. PubMed
Clinically silent LINE 1 insertion in the PNPLA3 gene may impede genotyping of the p.I148M variant