Author:
Talash Ghazal Alipour,Langfelder Peter,Vitale Daniele,Azardaryany Mahmoud Karimi,Belgard T. Grant,Choo Jocelyn,Rogers Geraint,Ho Vikki,Ramezani-Moghadam Mehdi,Dervish Suat,Lai Joey,Gloss Brian S.,McLeod Duncan,Eslam Mohammed,Liddle Chris,Qiao Liang,George Jacob,Esmaili Saeed
Abstract
ABSTRACTIn fatty liver disease, systemic homeostasis is perturbed. While pre-clinical models are used to understand its pathogenesis, translating this knowledge to patients is difficult. However, by focusing on the most preserved homeostasis systems between species and models, novel disease dimensions can be unearthed. We interrogated core liver gene co-expression networks in a mouse model of liver cancer following dietary challenge. Immunometabolic modules showed temporal changes under the influence of diet duration and aging. The behaviour of immune network in tumours mirrored their counterparts in non-tumour liver. A high immune response network was associated with a lower tumour burden in mice and humans. This module in mice was enriched for genes related to haematopoietic cell differentiation. Consistently, the bone marrow haematopoietic stem and progenitor cells response was reflective of the liver immune response. Linking haematopoiesis to hepatic homeostasis uncovers a hitherto unexplored dimension of tissue crosstalk that can inform pathogenesis.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献