Chakraborty A K, Ueda M, Mishima Y, Ichihashi M
Department of Dermatology, Yale University School of Medicine, New Haven, CT 06510.
Melanoma Res. 1992 Dec;2(5-6):315-9. doi: 10.1097/00008390-199212000-00004.
Levels of glutathione peroxidase (GSH-PX), glutathione-S-transferase (GST), gamma-glutamyl transpeptidase (gamma GTP) and glutathione reductase (GR) activities in the B16-F10 metastatic melanoma cell line are higher than those in non-metastatic B-16 murine melanoma cells. An inverse relationship was observed between the level of reduced glutathione (GSH) and metastatic capacity. Interferon (IFN), an antitumour and antimetastic agent, reduced the experimental metastatic capacity of B16-F10 cells while increasing the intracellular GSH content. This was associated with a fall in activity of GSH-metabolizing enzymes. These results suggest a correlation of intracellular GSH and its metabolizing enzymes with malignant transformation.
B16-F10转移性黑色素瘤细胞系中谷胱甘肽过氧化物酶(GSH-PX)、谷胱甘肽-S-转移酶(GST)、γ-谷氨酰转肽酶(γGTP)和谷胱甘肽还原酶(GR)的活性水平高于非转移性B-16小鼠黑色素瘤细胞。观察到还原型谷胱甘肽(GSH)水平与转移能力之间呈负相关。干扰素(IFN)是一种抗肿瘤和抗转移剂,它降低了B16-F10细胞的实验性转移能力,同时增加了细胞内GSH含量。这与GSH代谢酶活性的下降有关。这些结果表明细胞内GSH及其代谢酶与恶性转化之间存在相关性。