Longitudinal studies can identify distinct inflammatory cytokines associated with the inhibition or progression of liver cancer

医学 非酒精性脂肪肝 肝细胞癌 炎症 慢性肝病 疾病 内科学 肝癌 癌症 脂肪肝 免疫学 肝硬化 肿瘤科 生物信息学 生物
作者
Faridoddin Mirshahi,Hussein F. Aqbi,Kellen G. Cresswell,Mulugeta Saneshaw,Cara Coleman,Taylor Jacobs,Michael O. Idowu,Mikhail G. Dozmorov,Arun J. Sanyal,Masoud H. Manjili
出处
期刊:Liver International [Wiley]
卷期号:40 (2): 468-472 被引量:15
标识
DOI:10.1111/liv.14323
摘要

Abstract Background and Aims Chronic diseases such as nonalcoholic fatty liver disease (NAFLD) and hepatocellular carcinoma (HCC) are associated with chronic inflammation. However, controversial reports as to the key cytokines involved in the process of chronic inflammation hinder development of targeted therapies for patients. This is because, chronic inflammatory process cannot be fully understood by studying the mechanisms of the disease in a short‐term or isolated fashion. Understanding of the trend of inflammatory cytokines through longitudinal studies could provide a profound insight into the process of disease progression. Methods We performed a longitudinal analysis of inflammatory cytokines/chemokines and faecal microbiome dysbiosis associated with the diet‐induced progression of NAFLD to HCC in diet‐induced animal model of NAFLD comparing males and females, since males show a higher incidence of these diseases than females do. Results Longitudinal analyses revealed that a transient and timely increase in LIF and TMIP1 was associated with the inhibition of the progression of NAFLD to HCC in females. On the other hand, chronically increasing trends in CCL12, CCL17, CXCL9 and LIX/CXCL5 were associated with the promotion of the progression of NAFLD to HCC in males. Conclusions We provided empirical evidence that a methodological shift from snapshot observations to longitudinal data collection and analysis can provide a better understanding of chronic liver diseases.
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