Inhibitory effect of non-alcoholic steatohepatitis on colon cancer liver metastasis

医学 脂肪性肝炎 转移 内科学 结直肠癌 脂肪肝 内分泌学 肝癌 纤维化 车站3 胃肠病学 癌症 信号转导 疾病 生物 生物化学
作者
Shinichiro Yamada,Yuji Morine,Tetsuya Ikemoto,Yu Saito,Katsuki Miyazaki,Mayuko Ichimura‐Shimizu,Koichi Tsuneyama,Mitsuo Shimada
出处
期刊:Ejso [Elsevier BV]
卷期号:49 (2): 410-415 被引量:3
标识
DOI:10.1016/j.ejso.2022.11.002
摘要

The incidence of non-alcoholic steatohepatitis (NASH) is dramatically increasing, but the effect of NASH on colon cancer liver metastasis (CLM) is controversial. The aim of this study was to investigate the impact and mechanism of action of NASH on CLM using a western diet (WD)-fed mouse model.Six-week-old male C57BL/6 J mice were used. They were divided into the WD group and control group with normal diet. MC38 colon cancer cells were injected into the spleen at 2, 6, 8 and 16 weeks, and mice were killed at 2 weeks after injection to evaluate hepatic steatosis, fibrosis, metastasis and mRNA/protein expression in the liver.Only mice fed a WD for 16 weeks showed hepatic fibrosis. These mice showed significantly higher alanine aminotransferase and total cholesterol levels compared with the control group (p < 0.05). The WD group showed significantly lower tumor number and smaller tumor diameter (p < 0.05). In the WD group, expression of SAA1, IL6, STAT3 and MMP9 mRNA in the liver was significantly lower than in the control group (p < 0.05). Serum amyloid A1 protein expression was also lower in the WD group.The WD-fed NASH mouse model showed an inhibitory effect on CLM. Suppressed interleukin-6/signal transducer and activator of transcription 3 signaling and serum amyloid A/matrix metalloproteinase 9 expression may affect this phenomenon.
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