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Published in: Tumor Biology 1/2016

01-01-2016 | Review

IL-22: a promising candidate to inhibit viral-induced liver disease progression and hepatocellular carcinoma

Authors: Muhammad Saalim, Saleha Resham, Sobia Manzoor, Hassam Ahmad, Shahla Jaleel, Javed Ashraf, Muhammad Imran, Sidrah Naseem

Published in: Tumor Biology | Issue 1/2016

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Abstract

Hepatocellular carcinoma (HCC) is a growing concern all over the world. With the number of patients rising exponentially with each passing day, HCC is a problem that needs immediate attention. Currently, available treatment strategies focus on controlling the damage after the development of HCC. The options available from chemo- and radio-embolization to surgical resection and transplantation are not efficacious as required due to the complex nature of the disease. Liver regeneration and tissue healing are the subject of great interest today. Interleukin-22 (IL-22) is a cytokine with the ability to regenerate and therefore reverse the injuries caused by a wide range of agents. IL-22 acts via STAT molecule and controls the activity of a wide variety of cell survival and proliferation genes. Experimental data has given a positive insight into the role of IL-22 in inhibition of viral and alcohol-induced hepatocellular carcinoma. A further insight into the nature of IL-22 and the factors that can be manipulated in controlling the activity of IL-22 can help to counter the menace caused by the devastating effects of HCC.
Literature
2.
go back to reference Hassan MM, Hwang LY, Hatten CJ, Swaim M, Li D, Abbruzzese JL, et al. Risk factors for hepatocellular carcinoma: synergism of alcohol with viral hepatitis and diabetes mellitus. Hepatology. 2002;36(5):1206–13.CrossRefPubMed Hassan MM, Hwang LY, Hatten CJ, Swaim M, Li D, Abbruzzese JL, et al. Risk factors for hepatocellular carcinoma: synergism of alcohol with viral hepatitis and diabetes mellitus. Hepatology. 2002;36(5):1206–13.CrossRefPubMed
3.
go back to reference Marrero JA, Fontana RJ, Fu S, Conjeevaram HS, Su GL, Lok AS. Alcohol, tobacco and obesity are synergistic risk factors for hepatocellular carcinoma. J Hepatol. 2005;42(2):218–24.CrossRefPubMed Marrero JA, Fontana RJ, Fu S, Conjeevaram HS, Su GL, Lok AS. Alcohol, tobacco and obesity are synergistic risk factors for hepatocellular carcinoma. J Hepatol. 2005;42(2):218–24.CrossRefPubMed
4.
6.
go back to reference Block TM, Mehta AS, Fimmel CJ, Jordan R. Molecular viral oncology of hepatocellular carcinoma. Oncogene. 2003;22(33):5093–107.CrossRefPubMed Block TM, Mehta AS, Fimmel CJ, Jordan R. Molecular viral oncology of hepatocellular carcinoma. Oncogene. 2003;22(33):5093–107.CrossRefPubMed
7.
go back to reference Lindenbach BD, Rice CM. Unravelling hepatitis C virus replication from genome to function. Nature. 2005;436(7053):933–8.CrossRefPubMed Lindenbach BD, Rice CM. Unravelling hepatitis C virus replication from genome to function. Nature. 2005;436(7053):933–8.CrossRefPubMed
8.
go back to reference Levrero M. Viral hepatitis and liver cancer: the case of hepatitis C. Oncogene. 2006;25(27):3834–47.CrossRefPubMed Levrero M. Viral hepatitis and liver cancer: the case of hepatitis C. Oncogene. 2006;25(27):3834–47.CrossRefPubMed
9.
go back to reference Rehermann B. Hepatitis C, virus versus innate and adaptive immune responses: a tale of coevolution and coexistence. J Clin Invest. 2009;119(7):1745–54.CrossRefPubMedPubMedCentral Rehermann B. Hepatitis C, virus versus innate and adaptive immune responses: a tale of coevolution and coexistence. J Clin Invest. 2009;119(7):1745–54.CrossRefPubMedPubMedCentral
10.
go back to reference Dumoutier L, Louahed J, Renauld J-C. Cloning and characterization of IL-10-related T cell-derived inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9. J Immunol. 2000;164(4):1814–9.CrossRefPubMed Dumoutier L, Louahed J, Renauld J-C. Cloning and characterization of IL-10-related T cell-derived inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9. J Immunol. 2000;164(4):1814–9.CrossRefPubMed
11.
go back to reference Radaeva S, Sun R, Pan H, Hong F, Gao B, Interleukin 22. (IL‐22) plays a protective role in T cell‐mediated murine hepatitis: IL‐22 is a survival factor for hepatocytes via STAT3 activation. Hepatology. 2004;39(5):1332–42.CrossRefPubMed Radaeva S, Sun R, Pan H, Hong F, Gao B, Interleukin 22. (IL‐22) plays a protective role in T cell‐mediated murine hepatitis: IL‐22 is a survival factor for hepatocytes via STAT3 activation. Hepatology. 2004;39(5):1332–42.CrossRefPubMed
12.
go back to reference Dumoutier L, de Meester C, Tavernier J, Renauld J-C. New activation modus of STAT3 a tyrosine-less region of the interleukin-22 receptor recruits STAT3 by interacting with its coiled-coil domain. J Biol Chem. 2009;284(39):26377–84.CrossRefPubMedPubMedCentral Dumoutier L, de Meester C, Tavernier J, Renauld J-C. New activation modus of STAT3 a tyrosine-less region of the interleukin-22 receptor recruits STAT3 by interacting with its coiled-coil domain. J Biol Chem. 2009;284(39):26377–84.CrossRefPubMedPubMedCentral
13.
go back to reference Rawlings JS, Rosler KM, Harrison DA. The JAK/STAT signaling pathway. J Cell Sci. 2004;117(8):1281–3.CrossRefPubMed Rawlings JS, Rosler KM, Harrison DA. The JAK/STAT signaling pathway. J Cell Sci. 2004;117(8):1281–3.CrossRefPubMed
14.
go back to reference Bromberg J, Darnell Jr JE. The role of STATs in transcriptional control and their impact on cellular function. Oncogene. 2000;19(21):2468–73.CrossRefPubMed Bromberg J, Darnell Jr JE. The role of STATs in transcriptional control and their impact on cellular function. Oncogene. 2000;19(21):2468–73.CrossRefPubMed
15.
go back to reference Yoshida T, Hanada T, Tokuhisa T, Kosai K-I, Sata M, Kohara M. Activation of STAT3 by the hepatitis C virus core protein leads to cellular transformation. J Exp Med. 2002;196(5):641–53.CrossRefPubMedPubMedCentral Yoshida T, Hanada T, Tokuhisa T, Kosai K-I, Sata M, Kohara M. Activation of STAT3 by the hepatitis C virus core protein leads to cellular transformation. J Exp Med. 2002;196(5):641–53.CrossRefPubMedPubMedCentral
16.
go back to reference Gao B. Cytokines, STATs and liver disease. Cell Mol Immunol. 2005;2(2):92–100.PubMed Gao B. Cytokines, STATs and liver disease. Cell Mol Immunol. 2005;2(2):92–100.PubMed
18.
go back to reference Wang H, Lafdil F, Kong X, Gao B. Signal transducer and activator of transcription 3 in liver diseases: a novel therapeutic target. Int J Biol Sci. 2011;7(5):536.CrossRefPubMedPubMedCentral Wang H, Lafdil F, Kong X, Gao B. Signal transducer and activator of transcription 3 in liver diseases: a novel therapeutic target. Int J Biol Sci. 2011;7(5):536.CrossRefPubMedPubMedCentral
19.
go back to reference Nagem RAP, Colau D, Dumoutier L, Renauld J-C, Ogata C, Polikarpov I. Crystal structure of recombinant human interleukin-22. Structure. 2002;10(8):1051–62.CrossRefPubMed Nagem RAP, Colau D, Dumoutier L, Renauld J-C, Ogata C, Polikarpov I. Crystal structure of recombinant human interleukin-22. Structure. 2002;10(8):1051–62.CrossRefPubMed
20.
go back to reference de Oliveira NM, Ferreira Jr JR, Colau D, Fischer H, Nascimento AS, Craievich AF, et al. Interleukin-22 forms dimers that are recognized by two interleukin-22R1 receptor chains. Biophys J. 2008;94(5):1754–65.CrossRef de Oliveira NM, Ferreira Jr JR, Colau D, Fischer H, Nascimento AS, Craievich AF, et al. Interleukin-22 forms dimers that are recognized by two interleukin-22R1 receptor chains. Biophys J. 2008;94(5):1754–65.CrossRef
21.
go back to reference Foster RG, Golden-Mason L, Rutebemberwa A, Rosen HR. Interleukin (IL)-17/IL-22-producing T cells enriched within the liver of patients with chronic hepatitis C viral (HCV) infection. Dig Dis Sci. 2012;57(2):381–9.CrossRefPubMed Foster RG, Golden-Mason L, Rutebemberwa A, Rosen HR. Interleukin (IL)-17/IL-22-producing T cells enriched within the liver of patients with chronic hepatitis C viral (HCV) infection. Dig Dis Sci. 2012;57(2):381–9.CrossRefPubMed
22.
go back to reference Okuhara S, Umemura T, Joshita S, Shibata S, Kimura T, Morita S et al. Serum levels of interleukin‐22 and hepatitis B core‐related antigen are associated with treatment response to entecavir therapy in chronic hepatitis B. Hepatology Research. 2014. Okuhara S, Umemura T, Joshita S, Shibata S, Kimura T, Morita S et al. Serum levels of interleukin‐22 and hepatitis B core‐related antigen are associated with treatment response to entecavir therapy in chronic hepatitis B. Hepatology Research. 2014.
23.
go back to reference Dambacher J, Beigel F, Zitzmann K, Heeg MH, Göke B, Diepolder HM, et al. The role of interleukin-22 in hepatitis C virus infection. Cytokine. 2008;41(3):209–16.CrossRefPubMed Dambacher J, Beigel F, Zitzmann K, Heeg MH, Göke B, Diepolder HM, et al. The role of interleukin-22 in hepatitis C virus infection. Cytokine. 2008;41(3):209–16.CrossRefPubMed
24.
go back to reference Ki SH, Park O, Zheng M, Morales‐Ibanez O, Kolls JK, Bataller R, et al. Interleukin‐22 treatment ameliorates alcoholic liver injury in a murine model of chronic‐binge ethanol feeding: role of signal transducer and activator of transcription 3. Hepatology. 2010;52(4):1291–300.CrossRefPubMedPubMedCentral Ki SH, Park O, Zheng M, Morales‐Ibanez O, Kolls JK, Bataller R, et al. Interleukin‐22 treatment ameliorates alcoholic liver injury in a murine model of chronic‐binge ethanol feeding: role of signal transducer and activator of transcription 3. Hepatology. 2010;52(4):1291–300.CrossRefPubMedPubMedCentral
25.
go back to reference Støy S, Sandahl TD, Dige AK, Agnholt J, Rasmussen TK, Grønbæk H, et al. Highest frequencies of interleukin-22-producing T helper cells in alcoholic hepatitis patients with a favourable short-term course. PLoS One. 2013;8(1), e55101.CrossRefPubMedPubMedCentral Støy S, Sandahl TD, Dige AK, Agnholt J, Rasmussen TK, Grønbæk H, et al. Highest frequencies of interleukin-22-producing T helper cells in alcoholic hepatitis patients with a favourable short-term course. PLoS One. 2013;8(1), e55101.CrossRefPubMedPubMedCentral
26.
go back to reference Ashour TH. Therapy with interleukin-22 alleviates hepatic injury and hemostasis dysregulation in rat model of acute liver failure. Advances in hematology. 2014; 2014. Ashour TH. Therapy with interleukin-22 alleviates hepatic injury and hemostasis dysregulation in rat model of acute liver failure. Advances in hematology. 2014; 2014.
28.
go back to reference Gurtsevitch V. Human oncogenic viruses: hepatitis B and hepatitis C viruses and their role in hepatocarcinogenesis. Biochem Mosc. 2008;73(5):504–13.CrossRef Gurtsevitch V. Human oncogenic viruses: hepatitis B and hepatitis C viruses and their role in hepatocarcinogenesis. Biochem Mosc. 2008;73(5):504–13.CrossRef
29.
go back to reference Farazi PA, DePinho RA. Hepatocellular carcinoma pathogenesis: from genes to environment. Nat Rev Cancer. 2006;6(9):674–87.CrossRefPubMed Farazi PA, DePinho RA. Hepatocellular carcinoma pathogenesis: from genes to environment. Nat Rev Cancer. 2006;6(9):674–87.CrossRefPubMed
30.
go back to reference Kitaoka S, Shiota G, Kawasaki H. Serum levels of interleukin-10, interleukin-12 and soluble interleukin-2 receptor in chronic liver disease type C. Hepato-Gastroenterology. 2002;50(53):1569–74. Kitaoka S, Shiota G, Kawasaki H. Serum levels of interleukin-10, interleukin-12 and soluble interleukin-2 receptor in chronic liver disease type C. Hepato-Gastroenterology. 2002;50(53):1569–74.
31.
go back to reference Huang Y, Hwang S, Chan C, Wu J, Chao Y, Chang F, et al. Serum levels of cytokines in hepatitis C-related liver disease: a longitudinal study. Zhonghua yi xue za zhi = Chinese medical journal. Free China ed. 1999;62(6):327–33. Huang Y, Hwang S, Chan C, Wu J, Chao Y, Chang F, et al. Serum levels of cytokines in hepatitis C-related liver disease: a longitudinal study. Zhonghua yi xue za zhi = Chinese medical journal. Free China ed. 1999;62(6):327–33.
32.
go back to reference Sato T, Asanuma Y, Masaki Y, Sato Y, Hatakeyama Y, Kusano T, et al. Changes in tumor necrosis factor-a and interleukin-1 beta production following liver surgery on cirrhotic patients. Hepato-Gastroenterology. 1995;43(11):1148–53. Sato T, Asanuma Y, Masaki Y, Sato Y, Hatakeyama Y, Kusano T, et al. Changes in tumor necrosis factor-a and interleukin-1 beta production following liver surgery on cirrhotic patients. Hepato-Gastroenterology. 1995;43(11):1148–53.
33.
go back to reference Lejeune D, Dumoutier L, Constantinescu S, Kruijer W, Schuringa JJ, Renauld J-C. Interleukin-22 (IL-22) activates the JAK/STAT, ERK, JNK, and p38 MAP kinase pathways in a rat hepatoma cell line pathways that are shared with and distinct from IL-10. J Biol Chem. 2002;277(37):33676–82.CrossRefPubMed Lejeune D, Dumoutier L, Constantinescu S, Kruijer W, Schuringa JJ, Renauld J-C. Interleukin-22 (IL-22) activates the JAK/STAT, ERK, JNK, and p38 MAP kinase pathways in a rat hepatoma cell line pathways that are shared with and distinct from IL-10. J Biol Chem. 2002;277(37):33676–82.CrossRefPubMed
34.
go back to reference Boniface K, Bernard F-X, Garcia M, Gurney AL, Lecron J-C, Morel F. IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes. J Immunol. 2005;174(6):3695–702.CrossRefPubMed Boniface K, Bernard F-X, Garcia M, Gurney AL, Lecron J-C, Morel F. IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes. J Immunol. 2005;174(6):3695–702.CrossRefPubMed
35.
go back to reference Wolk K, Witte E, Wallace E, Döcke WD, Kunz S, Asadullah K, et al. IL‐22 regulates the expression of genes responsible for antimicrobial defense, cellular differentiation, and mobility in keratinocytes: a potential role in psoriasis. Eur J Immunol. 2006;36(5):1309–23.CrossRefPubMed Wolk K, Witte E, Wallace E, Döcke WD, Kunz S, Asadullah K, et al. IL‐22 regulates the expression of genes responsible for antimicrobial defense, cellular differentiation, and mobility in keratinocytes: a potential role in psoriasis. Eur J Immunol. 2006;36(5):1309–23.CrossRefPubMed
36.
go back to reference Pan H, Hong F, Radaeva S, Gao B. Hydrodynamic gene delivery of interleukin-22 protects the mouse liver from concanavalin A-, carbon tetrachloride-, and Fas ligand-induced injury via activation of STAT3. Cell Mol Immunol. 2004;1(1):43–9.PubMed Pan H, Hong F, Radaeva S, Gao B. Hydrodynamic gene delivery of interleukin-22 protects the mouse liver from concanavalin A-, carbon tetrachloride-, and Fas ligand-induced injury via activation of STAT3. Cell Mol Immunol. 2004;1(1):43–9.PubMed
37.
go back to reference Andoh A, Zhang Z, Inatomi O, Fujino S, Deguchi Y, Araki Y, et al. Interleukin-22, a member of the IL-10 subfamily, induces inflammatory responses in colonic subepithelial myofibroblasts. Gastroenterology. 2005;129(3):969–84.CrossRefPubMed Andoh A, Zhang Z, Inatomi O, Fujino S, Deguchi Y, Araki Y, et al. Interleukin-22, a member of the IL-10 subfamily, induces inflammatory responses in colonic subepithelial myofibroblasts. Gastroenterology. 2005;129(3):969–84.CrossRefPubMed
38.
go back to reference Zenewicz LA, Yancopoulos GD, Valenzuela DM, Murphy AJ, Karow M, Flavell RA. Interleukin-22 but not interleukin-17 provides protection to hepatocytes during acute liver inflammation. Immunity. 2007;27(4):647–59.CrossRefPubMedPubMedCentral Zenewicz LA, Yancopoulos GD, Valenzuela DM, Murphy AJ, Karow M, Flavell RA. Interleukin-22 but not interleukin-17 provides protection to hepatocytes during acute liver inflammation. Immunity. 2007;27(4):647–59.CrossRefPubMedPubMedCentral
39.
go back to reference Park O, Wang H, Weng H, Feigenbaum L, Li H, Yin S, et al. In vivo consequences of liver‐specific interleukin‐22 expression in mice: implications for human liver disease progression. Hepatology. 2011;54(1):252–61.CrossRefPubMedPubMedCentral Park O, Wang H, Weng H, Feigenbaum L, Li H, Yin S, et al. In vivo consequences of liver‐specific interleukin‐22 expression in mice: implications for human liver disease progression. Hepatology. 2011;54(1):252–61.CrossRefPubMedPubMedCentral
40.
go back to reference Kong X, Feng D, Wang H, Hong F, Bertola A, Wang FS, et al. Interleukin‐22 induces hepatic stellate cell senescence and restricts liver fibrosis in mice. Hepatology. 2012;56(3):1150–9.CrossRefPubMedPubMedCentral Kong X, Feng D, Wang H, Hong F, Bertola A, Wang FS, et al. Interleukin‐22 induces hepatic stellate cell senescence and restricts liver fibrosis in mice. Hepatology. 2012;56(3):1150–9.CrossRefPubMedPubMedCentral
41.
go back to reference Kong X, Feng D, Mathews S, Gao B. Hepatoprotective and anti‐fibrotic functions of interleukin‐22: therapeutic potential for the treatment of alcoholic liver disease. J Gastroenterol Hepatol. 2013;28(S1):56–60.CrossRefPubMedPubMedCentral Kong X, Feng D, Mathews S, Gao B. Hepatoprotective and anti‐fibrotic functions of interleukin‐22: therapeutic potential for the treatment of alcoholic liver disease. J Gastroenterol Hepatol. 2013;28(S1):56–60.CrossRefPubMedPubMedCentral
42.
go back to reference W-w X, M-j Z, Liu S, Xu T, Gao J, Wang J-x, et al. Hepatoprotective effects of IL-22 on fulminant hepatic failure induced by d-galactosamine and lipopolysaccharide in mice. Cytokine. 2011;56(2):174–9.CrossRef W-w X, M-j Z, Liu S, Xu T, Gao J, Wang J-x, et al. Hepatoprotective effects of IL-22 on fulminant hepatic failure induced by d-galactosamine and lipopolysaccharide in mice. Cytokine. 2011;56(2):174–9.CrossRef
43.
go back to reference Liang SC, Nickerson-Nutter C, Pittman DD, Carrier Y, Goodwin DG, Shields KM, et al. IL-22 induces an acute-phase response. J Immunol. 2010;185(9):5531–8.CrossRefPubMed Liang SC, Nickerson-Nutter C, Pittman DD, Carrier Y, Goodwin DG, Shields KM, et al. IL-22 induces an acute-phase response. J Immunol. 2010;185(9):5531–8.CrossRefPubMed
44.
go back to reference Ho HH, Ivashkiv LB. Role of STAT3 in type I interferon responses negative regulation of STAT1-dependent inflammatory gene activation. J Biol Chem. 2006;281(20):14111–8.CrossRefPubMed Ho HH, Ivashkiv LB. Role of STAT3 in type I interferon responses negative regulation of STAT1-dependent inflammatory gene activation. J Biol Chem. 2006;281(20):14111–8.CrossRefPubMed
45.
go back to reference Zhang Y, Ji H, Liu Y, Shen X, Gao F, Fong C et al., editors. The immunomodulatory role of IL-22 in mouse liver ischemia and reperfusion injury (IRI): enhancement of autophagy by STAT3-c-myc signaling. American Journal of Transplantation; 2013: Wiley-Blackwell 111 River ST, Hoboken 07030-5774, NJ USA. Zhang Y, Ji H, Liu Y, Shen X, Gao F, Fong C et al., editors. The immunomodulatory role of IL-22 in mouse liver ischemia and reperfusion injury (IRI): enhancement of autophagy by STAT3-c-myc signaling. American Journal of Transplantation; 2013: Wiley-Blackwell 111 River ST, Hoboken 07030-5774, NJ USA.
46.
go back to reference Zhao J, Zhang Z, Luan Y, Zou Z, Sun Y, Li Y, et al. Pathological functions of interleukin‐22 in chronic liver inflammation and fibrosis with hepatitis B virus infection by promoting T helper 17 cell recruitment. Hepatology. 2014;59(4):1331–42.CrossRefPubMedPubMedCentral Zhao J, Zhang Z, Luan Y, Zou Z, Sun Y, Li Y, et al. Pathological functions of interleukin‐22 in chronic liver inflammation and fibrosis with hepatitis B virus infection by promoting T helper 17 cell recruitment. Hepatology. 2014;59(4):1331–42.CrossRefPubMedPubMedCentral
47.
go back to reference Zhang Y, Cobleigh MA, Lian JQ, Huang CX, Booth CJ, Bai XF, et al. A proinflammatory role for interleukin-22 in the immune response to hepatitis B virus. Gastroenterology. 2011;141(5):1897–906.CrossRefPubMedPubMedCentral Zhang Y, Cobleigh MA, Lian JQ, Huang CX, Booth CJ, Bai XF, et al. A proinflammatory role for interleukin-22 in the immune response to hepatitis B virus. Gastroenterology. 2011;141(5):1897–906.CrossRefPubMedPubMedCentral
48.
go back to reference Chestovich PJ, Uchida Y, Chang W, Ajalat M, Lassman C, Sabat R, et al. IL-22: implications for liver ischemia/reperfusion injury. Transplantation. 2012;93(5):485.CrossRefPubMedPubMedCentral Chestovich PJ, Uchida Y, Chang W, Ajalat M, Lassman C, Sabat R, et al. IL-22: implications for liver ischemia/reperfusion injury. Transplantation. 2012;93(5):485.CrossRefPubMedPubMedCentral
49.
go back to reference Feng D, Wang Y, Wang H, Weng H, Kong X, Martin-Murphy BV, et al. Acute and chronic effects of IL-22 on acetaminophen-induced liver injury. J Immunol. 2014;193(5):2512–8.CrossRefPubMedPubMedCentral Feng D, Wang Y, Wang H, Weng H, Kong X, Martin-Murphy BV, et al. Acute and chronic effects of IL-22 on acetaminophen-induced liver injury. J Immunol. 2014;193(5):2512–8.CrossRefPubMedPubMedCentral
50.
go back to reference Zhang Z, Zhao J, Fu Y, Wang F-S. Increased IL-22-producing cells contribute to liver fibrosis through promoting Th17 migration in chronic HBV patients (P3363). The Journal of Immunology. 2013;190 (meeting abstracts 1):202.4. Zhang Z, Zhao J, Fu Y, Wang F-S. Increased IL-22-producing cells contribute to liver fibrosis through promoting Th17 migration in chronic HBV patients (P3363). The Journal of Immunology. 2013;190 (meeting abstracts 1):202.4.
51.
go back to reference Jiang R, Tan Z, Deng L, Chen Y, Xia Y, Gao Y, et al. Interleukin‐22 promotes human hepatocellular carcinoma by activation of STAT3. Hepatology. 2011;54(3):900–9.CrossRefPubMed Jiang R, Tan Z, Deng L, Chen Y, Xia Y, Gao Y, et al. Interleukin‐22 promotes human hepatocellular carcinoma by activation of STAT3. Hepatology. 2011;54(3):900–9.CrossRefPubMed
Metadata
Title
IL-22: a promising candidate to inhibit viral-induced liver disease progression and hepatocellular carcinoma
Authors
Muhammad Saalim
Saleha Resham
Sobia Manzoor
Hassam Ahmad
Shahla Jaleel
Javed Ashraf
Muhammad Imran
Sidrah Naseem
Publication date
01-01-2016
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 1/2016
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-015-4294-1

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