Effect of toll‐like receptor 7 and 9 targeted therapy to prevent the development of hepatocellular carcinoma. (30th July 2014)

• Record Type: Journal Article
• Authors: Mohamed, Fatma E.; Al‐Jehani, Rajai M.; Minogue, Shane S.; Andreola, Fausto; Winstanley, Alison; Olde Damink, Steven W.M.; Habtesion, Abeba; Malagó, Massimo; Davies, Nathan; Luong, Tu Vinh; Dhillon, Amar P.; Mookerjee, Rajeshwar P.; Dhar, Dipok K.; Jalan, Rajiv
• Is Part Of: Liver international. Volume 35:Number 3(2015:Mar.)
• Page Start: 1063
• Page End: 1076
• Publication Date: 2014-07-30
• Subjects: Liver -- Periodicals; Liver -- Diseases -- Periodicals; 616.362
• DOI: 10.1111/liv.12626
• Languages: English
• ISSNs: 1478-3223

Abstract

<abstract abstract-type="main" id="liv12626-abs-0001"> <title>Abstract</title> <sec id="liv12626-sec-0001" sec-type="section"> <title>Background & Aims</title> <p>Chronic liver disease is a predisposing factor for development of hepatocellular carcinoma (HCC). Toll‐like receptors play a crucial role in immunity against microbial pathogens and recent evidence suggests that they may also be important in pathogenesis of chronic liver disease. The purpose of this study was to determine whether TLR7 and TLR9 are potential targets for prevention and progression of HCC.</p> </sec> <sec id="liv12626-sec-0002" sec-type="section"> <title>Methods</title> <p>Tissue microarrays containing liver samples from patients with cirrhosis, viral hepatitis and HCC were examined for expression of TLR7 and TLR9 and the data obtained was validated in liver specimens from the hospital archives. Proliferation of human HCC cell lines was studied following stimulation of TLR7 and TLR9 using agonists (imiquimod and CpG‐ODN respectively) and inhibition with a specific antagonist (IRS‐954) or chloroquine. The effect of these interventions was confirmed in a xenograft model and diethylnitrosamine (DEN)/nitrosomorpholine (NMOR)‐induced model of HCC.</p> </sec> <sec id="liv12626-sec-0003" sec-type="section"> <title>Results</title> <p>TLR7 and TLR9 expression was up‐regulated in human HCC tissue. Proliferation of HuH7 cells <italic>in vitro</italic> increased significantly in response to stimulation of TLR7. TLR7 and TLR9 inhibition using IRS‐954 or chloroquine significantly reduced HuH7 cell proliferation <italic>in vitro</italic> and inhibited tumour growth in the mouse xenograft model. HCC development in the DEN/NMOR rat model was also significantly inhibited by chloroquine (<italic>P</italic> < 0.001).</p> </sec> <sec id="liv12626-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The data suggest that inhibiting TLR7 and TLR9 with IRS‐954 or chloroquine could potentially be used as a novel therapeutic approach for preventing HCC development and/or progression in susceptible patients.</p> </sec> </abstract>