DiSorbo D M, Litwack G
Nutr Cancer. 1982;3(4):216-22. doi: 10.1080/01635588109513725.
Data are presented which indicate that vitamin B6 (pyridoxine) can retard and eventually kill Fu5-5 rat hepatoma cells in culture. Additional studies indicate that the human kidney cell line 293-31, and a rat glial cell strain. C6, display growth characteristics similar to those of hepatoma cells when cultured in 5 mM pyridoxine-supplemented medium. However, the pyridoxine-supplemented culture medium had little effect on the growth of the human mammary cancer cell line MCF-7. The resistance of the MCF-7 cells to growth inhibition by vitamin B6 suggests that the vitamer pyridoxine must be metabolized by pyridoxal before it can act as a growth inhibitor. These findings suggest the potential use of vitamin B6 as an antineoplastic agent. Possible mechanisms by which vitamin B6 promotes this effect are presented.
所呈现的数据表明,维生素B6(吡哆醇)在培养过程中可延缓并最终杀死Fu5-5大鼠肝癌细胞。进一步的研究表明,人肾细胞系293-31和大鼠神经胶质细胞系C6在添加5 mM吡哆醇的培养基中培养时,显示出与肝癌细胞相似的生长特性。然而,添加吡哆醇的培养基对人乳腺癌细胞系MCF-7的生长影响很小。MCF-7细胞对维生素B6生长抑制的抗性表明,维生素吡哆醇在作为生长抑制剂起作用之前必须先被吡哆醛代谢。这些发现提示维生素B6作为一种抗肿瘤药物的潜在用途。本文还介绍了维生素B6产生这种作用的可能机制。