2012
DOI: 10.1002/cbf.2905
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Hesperetin impairs glucose uptake and inhibits proliferation of breast cancer cells

Abstract: The flavanone hesperetin is known to decrease basal glucose uptake, although the inhibitory mechanism is largely unknown. Here, we used MDA-MB-231 breast cancer cells to investigate the molecular pathways affected by hesperetin. The results indicate that the suppression of glucose uptake is caused by the down-regulation of glucose transporter 1 (GLUT1). Hesperetin was also found to inhibit insulin-induced glucose uptake through impaired cell membrane translocation of glucose transporter 4 (GLUT4). In addition,… Show more

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Cited by 104 publications
(62 citation statements)
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“…Indeed, harmful solvents have been used extensively in vitro and in vivo to permit the delivery of non-water-soluble drugs. For instance, dimethyl sulfoxide (DMSO) is usually the first agent of choice for cell culture [34, 35]. However, DMSO has displayed toxicity in multiple studies [3639].…”
Section: Reduction Of Drug Toxicity Through Nanomedicinementioning
confidence: 99%
“…Indeed, harmful solvents have been used extensively in vitro and in vivo to permit the delivery of non-water-soluble drugs. For instance, dimethyl sulfoxide (DMSO) is usually the first agent of choice for cell culture [34, 35]. However, DMSO has displayed toxicity in multiple studies [3639].…”
Section: Reduction Of Drug Toxicity Through Nanomedicinementioning
confidence: 99%
“…RNA extraction was performed using the ALLPrep RNA Kit (QIAGEN), according to the manufacturer's instructions, and samples were quantified by absorption spectroscopy. Real‐time RT‐PCR was conducted as previously described [15].…”
Section: Methodsmentioning
confidence: 99%
“…In addition, the binding of CDK4 with p21Cip1 was boosted by hesperetin, showing their involvement in anti-cancer activity in MCF-7 cells. Hesperetin impaired the uptake of insulin-generated glucose and inhibited proliferation in MDA-MB-231 cancer cells 112 . This was followed by inhibition of insulin-related redistribution of GLUT4, phosphorylation of insulin receptor and AKT, finally causing antiproliferation of breast cancer cells.…”
Section: Hesperetinmentioning
confidence: 97%