British Journal of Dermatology · 1986 · 30 citations · 13 references
Life SciencesBiochemistryCell BiologyCellular MetabolismMetabolismMitochondrial BiologyCellular ToxicologyMitochondrial BioenergeticsMitochondrial FunctionMitochondrial MetabolismMitochondrial ToxicityTricarboxylic Acid CycleDicarboxylic Acid MetabolismDicarboxylic AcidsEnzymesMelanin BiosynthesisMelanin FormationMelanin SynthesisMelanocyte BiologyMitochondrial Toxicity Mechanisms
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.
13
The Journal of Investigative Dermatology
Naomi M. Kanof · Archives of Dermatology · 1967 · 1.4K citations
Journal of the National Cancer Institute
Journal of the American Dietetic Association · 1994 · 172 citations
THE ISOLATION AND CYTOLOGY OF TWO PIGMENT CELL STRAINS FROM B-16 MOUSE MELANOMAS.
Funan Hu, Patricia F. Lesney · PubMed · 1964 · 102 citations
Medicine, Cell Biology, Oncology +16
EFFECT OF AZELAIC ACID ON HUMAN MALIGNANT MELANOMA
M. Nazzaro-Porro, G Zina, A. S. Breathnach et al. · The Lancet · 1980 · 70 citations
Medicine, Oncology, Pharmacology +10
Effect of Dicarboxylic Acids on Lentigo Maligna
M. Nazzaro-Porro, Siro Passi, L. Båluş et al. · Journal of Investigative Dermatology · 1979 · 68 citations · Full text