胰腺癌
下调和上调
医学
脂肪酸结合蛋白
癌症
癌症研究
内科学
内分泌学
生长因子
PI3K/AKT/mTOR通路
脂肪酸
细胞生长
信号转导
生物
生物化学
基因
受体
作者
Keith M. Wirth,Shuhei Shinoda,Mizuho Sato‐Dahlman,Deborah M. Dickey,David Bernlohr,Sayeed Ikramuddin,Masato Yamamoto
标识
DOI:10.1016/j.soard.2021.12.002
摘要
Obesity and diabetes are associated with an increased incidence of pancreatic cancer. Fatty acid binding protein 4 (FABP4), noted to be higher in patients with severe obesity, is linked to the development and progression of several cancers, and its level in the circulation decreases after bariatric surgery.In this paper, we evaluate the role of FABP4 in pancreatic cancer progression.University Hospital and Laboratories, United States.When Panc-1 (human) and Pan02 (mouse) pancreatic cancer cells were treated with FABP4 or the-single-point mutant FABP4 (R126Q, fatty acid binding site mutant), only FABP4 stimulated cellular proliferation. The transcriptional activity of nuclear factor E2-related factor 2 (NRF2) was increased in response to FABP4 but not the R126Q. FABP4 treatment also led to downregulation of reactive oxygen species (ROS) activity. Consistent with induced cell propagation by FABP4, the growth of Pan02 tumor was decreased in FABP4-null animals compared with C57BL/6J controls.These results suggest that FABP4 increases pancreatic cancer proliferation via activation of NRF2 and downregulation of ROS activity.
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