Kimura Tomohiro, Shirakawa Ryutaro, Yaoita Nobuhiro, Hayashi Takashi, Nagano Keisuke, Horiuchi Hisanori
Department of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
Institute of Biomedical Innovation, Otsuka Pharmaceutical Co., Ltd., 463-10 Kagasuno, Kawauchi-cho, Tokushima 771-0192, Japan.
FEBS Lett. 2014 Oct 16;588(20):3673-6. doi: 10.1016/j.febslet.2014.08.011. Epub 2014 Aug 23.
Quinoline derivatives such as chloroquine and primaquine are widely used for the treatment of malaria. These drugs are also used for the treatment of trypanosomiasis, and more recently for cancer therapy. However, molecular target(s) of these drugs remain unclear. In this study, we have identified human pyridoxal kinase as a binding protein of primaquine. Primaquine inhibited pyridoxal kinases of malaria, trypanosome and human, while chloroquine inhibited only malaria pyridoxal kinase. Thus, we have identified pyridoxal kinase as a possible target molecule of the antimalarial drugs chloroquine and primaquine.
喹啉衍生物如氯喹和伯氨喹被广泛用于治疗疟疾。这些药物也用于治疗锥虫病,最近还用于癌症治疗。然而,这些药物的分子靶点仍不清楚。在本研究中,我们已确定人吡哆醛激酶是伯氨喹的结合蛋白。伯氨喹抑制疟疾、锥虫和人类的吡哆醛激酶,而氯喹仅抑制疟疾吡哆醛激酶。因此,我们已确定吡哆醛激酶是抗疟药物氯喹和伯氨喹的一个可能靶点分子。