胰腺癌
胰腺肿瘤
内科学
上皮-间质转换
细胞凋亡
细胞因子
血管生成
癌症
体内
医学
癌症研究
内分泌学
生物
转移
生物化学
生物技术
作者
Denise I. Garcia,Katie E. Hurst,Alexandra Bradshaw,Harinarayanan Janakiraman,Cindy Wang,E. Ramsay Camp
标识
DOI:10.1016/j.jss.2020.10.007
摘要
Abstract: Background Emerging evidence indicates associations between high-fat diet (HFD), metabolic syndrome (MetS), and increased risk of pancreatic cancer. However, individual components of an HFD that increase cancer risk have not been isolated. In addition, a specific pattern of cytokine elevation by which MetS drives pancreatic tumor progression is not well described. We hypothesized that oleic acid (OA), a major component of HFD, would augment pancreatic neoplastic processes. Methods An orthotopic pancreatic cancer model with Panc02 cells was used to compare the effect of low-fat diet to OA-based HFD on cancer progression. Tumors were quantitated, analyzed by immunohistochemistry. In addition, serum cytokine levels were quantitated. Proliferation, migration assays, and expression of epithelial-to-mesenchymal transition factors were evaluated on Panc02 and MiaPaCa-2 pancreatic cancer cells cultured in high concentrations of OA. Results HFD tumor-bearing mice (n = 8) had an 18% weight increase (P 2.5-fold increase in cell migration (P Conclusions High-fat conditions in vitro and in vivo resulted in an aggressive pancreatic cancer phenotype. Our data support further investigations elucidating molecular pathways augmented by MetS conditions to identify novel therapeutic strategies for pancreatic cancer.
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