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Ganoderma tsugae extract inhibits expression of epidermal growth factor receptor and angiogenesis in human epidermoid carcinoma cells: In vitro and in vivo
Authors:Shih-Chung Hsu  Chien-Chih Ou  Tzu-Chao Chuang  Jhy-Wei Li  Yi-Jen Lee  Vinchi Wang  Jah-Yao Liu  Chin-Shiang Chen  Song-Chow Lin  Ming-Ching Kao
Affiliation:1. Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan, ROC;2. Kang-Ning Junior College of Medical Care and Management, Taipei, Taiwan, ROC;3. Department of Obstetrics and Gynecology, Tri-Service General Hospital, Taipei, Taiwan, ROC;4. Department of Chemistry, Tamkang University, Tamsui, Taipei, Taiwan, ROC;5. Graduate Institute of Life Sciences, Tamkang University, Tamsui, Taipei, Taiwan, ROC;6. Graduate Institute of Pathology, National Defense Medical Center, Taipei, Taiwan, ROC;g Department of Pathology, Da-Chien General Hospital, Miaoli, Taiwan, ROC;h Department of Neurology, Cardinal Tien Hospital, Taipei, Taiwan, ROC;i School of Medicine, Fu-Jen Catholic University, Taipei, Taiwan, ROC;j Department of Horticulture and Biotechnology, Chinese Culture University, Taipei, Taiwan, ROC;k School of Biological Science and Technology, China Medical University, Taichung, Taiwan, ROC;l Department of Biochemistry, National Defense Medical Center, Taipei, Taiwan, ROC
Abstract:We examined the anti-angiogenic effects of Ganoderma tsugae methanol extract (GTME) on human epidermoid carcinoma A-431 cells. Our data indicate that GTME inhibits the expression of epidermal growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) in vitro and in vivo, and also inhibits the capillary tube formation of human umbilical vein endothelial cells (HUVECs). We also show that the suppression of VEGF expression by GTME can be restored by treatment with EGF. These results suggest that GTME inhibits VEGF expression via the suppression of EGFR expression, resulting in the downregulation of VEGF secretion from epidermoid carcinoma A-431 cells. These findings reveal a novel role for G. tsugae in inhibiting EGFR and VEGF expression, which are important for tumor angiogenesis and growth. Thus, GTME may provide a potential therapeutic approach for anti-tumor treatment.
Keywords:G. tsugae, Ganoderma tsugae   GTME, Ganoderma tsugae methanol extract   EGFR, epidermal growth factor receptor   VEGF, vascular endothelial growth factor   MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide   HUVECs, human umbilical vein endothelial cells
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