From the Department of Surgery, Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Departments of Biotechnology.
Pancreas. 2021 Apr 1;50(4):564-570. doi: 10.1097/MPA.0000000000001797.
High-fat diet has been considered a risk factor for the development of pancreatic cancer. It is also shown to significantly impact composition and dysbiosis of gut microbiota in both humans and animals. However, there is little information on the effect of high-fat diet on the development of pancreatic cancer or upon the gut microbiota of patients with pancreatic cancer in humans or animal models.
In this study, the effect of high-fat diet on cancer pathology and the gut microbiota was investigated by a carcinogen-induced pancreatic cancer mouse model.
Compared with carcinogen alone, mice with high-fat diet and carcinogen showed more obvious pathological changes in pancreatic tissue; increased levels of proinflammatory cytokine tumor necrosis factor-α, interleukin-6, interleukin-10, and carbohydrate antigen 242; and increased expression of cancer-associated biomarkers mucin-4 and claudin-4 in pancreatic tissue. Moreover, there is a significant change in the gut microbiota between the carcinogen group and the carcinogen with high-fat diet group. We identified that Johnsonella ignava especially existed in the carcinogen with high-fat diet group, which may contribute to pancreatic cancer development.
Our results revealed that high-fat diet changed the composition of the gut microbiota and was involved in carcinogen-induced pancreatic cancer progression.
高脂肪饮食被认为是胰腺癌发展的一个风险因素。它也被证明会显著影响人和动物肠道微生物群落的组成和失调。然而,关于高脂肪饮食对人类或动物模型中胰腺癌发展或胰腺癌患者肠道微生物群落的影响的信息很少。
本研究通过致癌剂诱导的胰腺癌小鼠模型,研究了高脂肪饮食对癌症病理学和肠道微生物群的影响。
与致癌剂单独作用相比,高脂肪饮食和致癌剂组的小鼠胰腺组织出现更明显的病理变化;促炎细胞因子肿瘤坏死因子-α、白细胞介素-6、白细胞介素-10 和碳水化合物抗原 242 水平升高;胰腺组织中癌症相关生物标志物粘蛋白-4 和紧密连接蛋白-4 的表达增加。此外,致癌剂组和高脂肪饮食加致癌剂组之间的肠道微生物群落发生了显著变化。我们发现 Johnsonella ignava 特别存在于高脂肪饮食加致癌剂组中,这可能有助于胰腺癌的发展。
我们的结果表明,高脂肪饮食改变了肠道微生物群落的组成,并参与了致癌剂诱导的胰腺癌进展。