作者: Yong Yang , Joy Wolfram , Kathryn Boom , Xiaohong Fang , Haifa Shen
DOI: 10.1002/CBF.2905
关键词: Hesperidin 、 Biology 、 Glucose Transporter Type 1 、 Endocrinology 、 GLUT4 、 Hesperetin 、 Glucose transporter 、 GLUT1 、 Internal medicine 、 Glucose uptake 、 Protein kinase B
摘要: The flavanone hesperetin is known to decrease basal glucose uptake, although the inhibitory mechanism largely unknown. Here, we used MDA-MB-231 breast cancer cells investigate molecular pathways affected by hesperetin. results indicate that suppression of uptake caused down-regulation transporter 1 (GLUT1). Hesperetin was also found inhibit insulin-induced through impaired cell membrane translocation 4 (GLUT4). In addition, phosphorylation insulin receptor-beta subunit (IR-beta) and Akt suppressed. decreased cellular proliferation, which likely due inhibition uptake. Cancer are highly dependent on may, therefore, have potential application as an anticancer agent.