Hu F, Mah K, Teramura D J
Br J Dermatol. 1986 Jan;114(1):17-26. doi: 10.1111/j.1365-2133.1986.tb02775.x.
We have shown that dicarboxylic acids (C9 and C12), known competitive inhibitors of tyrosinase, are selectively cytotoxic to malignant melanogenic melanocytes but not to normal pigmented cells or to amelanotic or non-melanogenic melanoma cells. The main target of this toxicity appears to be the mitochondria, which become markedly swollen and vacuolated. The mechanism of their action has been thought to be due to interference with oxidoreductases in the mitochondria. However, our results suggest that this cytotoxicity most probably does not result simply from inhibition of mitochondrial enzymes, but is closely related to the melanin biosynthesis pathway.
我们已经表明,二羧酸(C9和C12),即已知的酪氨酸酶竞争性抑制剂,对恶性黑素生成性黑素细胞具有选择性细胞毒性,但对正常色素沉着细胞、无色素性或非黑素生成性黑色素瘤细胞则无毒性。这种毒性的主要靶点似乎是线粒体,线粒体明显肿胀并出现空泡化。其作用机制一直被认为是由于干扰了线粒体中的氧化还原酶。然而,我们的结果表明,这种细胞毒性很可能并非仅仅源于线粒体酶的抑制,而是与黑色素生物合成途径密切相关。