PI3K/AKT/GSK-3β signaling pathway involving in the mechanism of
polymyxin B induced melanogenesis
Abstract
Backgrounds: Polymyxin B, which is a last line antibiotic for
multi-drug resistant gram-negative bacteria, has been reported to induce
skin hyperpigmentation in patients during treatments.
8~15% or more cases were reported hyperpigmentation,
especially in head and neck, seriously influencing the compliance of
patients. To investigate the mechanism of hyperpigmentation is
beneficial for intervention strategy and improve compliance. Methods:
The melanoma cells, SK-MEL-2 cells were employed in the present study to
verify whether polymyxin B treatment could directly induce
hyperpigmentation. Melanin contents were measured by hot alkali lysis
method and tyrosinase were quantified by dopaquinone oxidation method.
The real-time quantitative PCR was applied to measure the mRNA levels of
melanogenesis-related genes to investigate the possible signaling
pathway involved in the polymyxin B induced hyperpigmentation. Results:
The melanin content and tyrosinase activity were up-regulated after 5
μg/mL polymyxin B treatment in SK-MEL-2 cells at 48 hr. and 72 hr. The
mRNA levels of melanogenesis-related genes were up-regulated, including
PI3K, Akt, GSK-3β, CREB, MITF in the polymyxin B treatment group
compared with control group at 48 hr. (p<0.001). Conclusions:
In the present study, for the first time to reveal that polymyxin B
induced hyperpigmentation involved the signaling pathway of
PI3K/AKT/GSK-3β and the up-regulation of CREB and MITF subsequently,
then induced the activity of tyrosinase and melanin content in melanoma
cells.