Exercise retards hepatocarcinogenesis in obese mice independently of weight control

التفاصيل البيبلوغرافية
العنوان: Exercise retards hepatocarcinogenesis in obese mice independently of weight control
المؤلفون: W. Geoffrey Haigh, Sharon Pok, Vanessa Barn, Geoffrey C. Farrell, Narci C. Teoh, Arfianti Arfianti, Matthew M. Yeh, George N. Ioannou
المصدر: Journal of Hepatology. 73:140-148
بيانات النشر: Elsevier BV, 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Carcinoma, Hepatocellular, Carcinogenesis, MAP Kinase Signaling System, Mice, Obese, Type 2 diabetes, Motor Activity, Mice, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Physical Conditioning, Animal, Proliferating Cell Nuclear Antigen, Diabetes mellitus, Internal medicine, Animals, Medicine, Obesity, Hepatology, business.industry, Body Weight, Liver Neoplasms, Fatty liver, Protective Factors, medicine.disease, Immunohistochemistry, digestive system diseases, 030104 developmental biology, Endocrinology, Diabetes Mellitus, Type 2, Hepatocellular carcinoma, 030211 gastroenterology & hepatology, Histopathology, Mitogen-Activated Protein Kinases, Tumor Suppressor Protein p53, business, Liver cancer
الوصف: Obesity and type 2 diabetes increase hepatocellular carcinoma (HCC) incidence in humans and accelerate diethylnitrosamine (DEN)-induced hepatocarcinogenesis in mice. We investigated whether exercise reduces HCC development in obese/diabetic Alms1 mutant (foz/foz) mice and studied protective mechanisms.We measured HCC development in DEN-injected male foz/foz and wild-type (WT) littermates housed with or without an exercise wheel from week 4 until 12 or 24 weeks, and in foz/foz mice pair-fed to WT littermates. We also studied HCC development in DEN-injected Jnk1Exercising foz/foz mice maintained similar weight as WT mice up to 10 weeks, but then gained weight and were obese by 24 weeks; a similar body weight profile was obtained by pair-feeding foz/foz mice to WT. At 12 weeks, livers of exercising foz/foz mice exhibited fewer GST-pi positive hepatocytes than sedentary counterparts; by 24 weeks, fewer exercising foz/foz mice developed HCC (15% vs. 64%, p0.05). Conversely, pair-feeding foz/foz mice failed to reduce HCC incidence. In these insulin-resistant foz/foz mice, exercise failed to activate hepatic AMPK or Akt/mTORC1. Instead, it improved insulin sensitivity, ameliorated steatosis and liver injury, activated p53 to increase p27 expression, and prevented JNK activation. This was associated with suppression of hepatocellular proliferation. DEN-injected Jnk1Direct effects of exercise dampen proliferation of dysplastic hepatocytes to reduce 3-month dysplastic foci and 6-month incidence of DEN-induced HCC in obese, insulin-resistant mice. The effects of exercise that potentially slow hepatocarcinogenesis include p53-mediated induction of p27 and prevention of JNK activation.Fatty liver disease commonly occurs alongside obesity and diabetes, contributing to rapidly increasing rates of liver cancer throughout the world. Herein, we show that exercise reduces the incidence and progression of hepatocellular carcinoma in mouse models. The effect of exercise on cancer risk was shown to be independent of changes in weight. Exercise could be a protective mechanism against liver cancer in at-risk individuals.
تدمد: 0168-8278
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2363ce76621d5314ee19f5cc834cca4
https://doi.org/10.1016/j.jhep.2020.02.006
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....e2363ce76621d5314ee19f5cc834cca4
قاعدة البيانات: OpenAIRE