CN Bio, a leading cell culture company that has developed single and multi-organ microphysiological systems (MPS) that improve the accuracy and efficiency of drug discovery, today announced the publication of co-authored research led by researchers at the University of Cambridge in Nature Metabolism1, identifying a novel pathway that regulates the underlying mechanism of Non-Alcoholic Steatohepatitis (NASH), potentially a new therapeutic target.
CN Bio and Cambridge University identify novel regulatory pathway driving NASH
The collaborative work uses CN Bio’s NASH model to help elucidate the complex cellular mechanisms that cause liver fibrosis.
The group demonstrated that Bone Morphogenetic Protein 8B (BMP8B), a poorly characterised member of the BMP/TGFß superfamily, exhibits marked upregulation during Non-Alcoholic Fatty Liver Disease (NAFLD) to NASH disease progression. This surge of BMP8B was shown to be an important mediator of liver disease progression, and a leading pathogenic mediator of the wound healing response of NASH, therefore presenting itself as a potential therapeutic target.
Contributing organisations include: University of Cambridge, Newcastle University, National & Kapodistrian University of Athens, Nordic Bioscience A/S, Sorbonne Université, Imperial College London and Wellcome Trust Sanger Institute
The paper illustrates the direct translation between CN Bio’s NASH assay, human clinical studies and in vivo mouse models. It demonstrates that the MPS NASH model can offer more human-relevant data than standard liver tissue studies, and a quicker and cheaper option to study NASH pathophysiology with similar results to long and expensive animal models to better inform the drug discovery process and reduce associated costs. Cell cultures were performed in CN Bio’s MPS NASH model, utilising its proprietary liver-on-chip technology, which enables longer term in vitro culture (>1 month) of primary human hepatocytes in 3D microtissue structures. The NASH assay captures all key aspects of the different stages of the NAFLD/NASH spectrum: intracellular fat accumulation, inflammation and fibrosis.
Dr David Hughes, CEO, CN Bio, commented: “Increasing global levels of obesity are paralleled with growing numbers of NASH patients. However, currently there are no therapies on the market to treat the disease, with candidates in phase 3 clinical trials not effective enough to treat the majority of patients. By providing human-relevant organ-on-chip data, our NASH model is enabling researchers to screen new NAFLD and NASH therapeutic candidates, investigate mechanisms of action and generate actionable data in weeks, ultimately to fast-track investigation into new drug candidates.”
Dr Tomasz Kostrzewski, Director, Biology, CN Bio, said: “This paper demonstrates how industry leaders in fatty liver disease, NASH and fibrosis have recognised the quality of CN Bio’s research and the reliability of our data. We’re excited to see this research published in Nature Metabolism, a new and exciting journal for our field which will become highly impactful.”
'Bone morphogenetic protein 8B promotes the progression of non-alcoholic steatohepatitis', Nature Metabolism, https://www.nature.com/articles/s42255-020-0214-9
CN Bio’s NASH model is available as a fee-for-service offering, performed and analysed using the Company’s PhysioMimix™ MPS. The offering supports researchers in planning and optimising clinical trial design, to prioritise pre-clinical candidates and integrate effects on different target cell types of the liver.
For more information about CN Bio’s NASH drug discovery fee-for-service, please visit: https://cn-bio.com/nash-fee-for-service/
CN Bio is a leading life sciences company. Our microfluidic technology improves drug discovery by generating human-relevant pre-clinical data in the lab, bridging gaps between traditional cell culture, animal studies, and human clinical trials to help develop safer, more effective, medicines, faster and reducing or replacing animal testing. Our Systems and Services facilitate deep insights into disease mechanisms, therapeutic efficacy and safety assessments.