Future
thought
One important pathway in melanin synthesis
involves the transcription factor MITF. The MITF gene is highly conserved
and is found in people, mice, birds, and even fish. MITF production
is regulated via a fairly straightforward pathway. UV radiation causes
increased expression of transcription factor p53 in keratinocytes, and
p53 causes these cells to produce melanocyte stimulating hormone (MSH),
which binds to melanocortin 1 receptors (MC1R) on melanocytes. Ligand-binding
at MC1R receptors activates adenyl cyclases, which produce cAMP, which
activates CREB, which promote MITF expression. The targets of MITF include
p16 (a CDK inhibitor) and Bcl2, a gene essential to melanocyte survival.
It is often difficult to design drugs that interfere with transcription
factors, but perhaps new drugs will be discovered that can impede some
reaction in the pathway upstream of MITF. Studies of chromatin structure
also promise to shed light on transcriptional regulation in melanoma
cells. It has long been assumed that nucleosomes are positioned randomly
on DNA, but murine studies of genes involved in melanin production now
suggest that nucleosomes are stereotypically positioned on DNA. When
a gene is undergoing transcription, its transcription start site is
almost always nucleosome-free. When the gene is silent, however, nucleosomes
often block the transcriptional start site, suggesting that nucleosome
position may play a role in gene regulation. Finally, given the fact
that tanning helps protect skin cells from UV-induced damage, new melanoma
prevention strategies could involve attempts to induce tanning in individuals
who would otherwise get sunburns. Redheads, for example, do not tan
because they have MC1R mutations. In mice, it has been shown that the
melanin production pathway can be rescued downstream of MC1R. Perhaps
such a strategy will eventually be used to protect humans from melanoma.