About two months ago, my father was
diagnosed with skin cancer. Fortunately, it was not a diagnosis of melanoma.
However, the diagnoses was still devastating and mortifying. He underwent
treatment shortly after and is now cancer free. The physician indicated the
skin cancer was a possible result of not applying sunscreen. Unlike my father,
I liberally apply sunscreen multiple times if I’m out in the sun for extended
periods of time. Unfortunately, I’m cursed with pale skin and burn easily. The
recent diagnoses of my father sparked my interest to read this scientific
study. The scientific study examined the molecular changes of the skin cells associated with skin cancer with and without sunscreen.
According to the article, melanoma
is a form of skin cancer that results from melanocytes, the pigment producing
cells of the skin. It is hypothesized that the increased production of
melanocytes may be associated with melanoma. The link between ultraviolet
radiation and melanoma are undetermined and farther investigation needs to be
conducted. The p53 gene plays an
important role in preventing skin cancer by repairing UV damaged skin. The p53
gene can be mutated overtime with increased exposure to ultraviolet radiation
and repeated burning of the skin. The mutated p53 gene displays a loss in the
capabilities to repair UV damaged skin resulting in the increased risk of skin
cancer.
According to the study, 24 hours after
solar-simulated ultraviolet radiation (SSUVR) keratinocytes and melanocytes
both skin cells displayed UV induced DNA damage. The unexposed skin and skin
protected with sunscreen displayed no UV induced DNA damage. The UV induced DNA
damage can increase the risk of melanoma. The application of sunscreen can
diminish DNA damage associated with ultraviolet radiation and reduce the risk
of melanoma and other skin cancers.
The expression of the p53 gene was
present in keratinocytes and melanocytes. The gene expression in both cells
increased 24 hours after being exposed to SSUVR, the expression of the gene
decreased at 14 days. The application of sunscreen displayed no p53 expression
in keratinocytes and melanocytes after exposure to SSUVR. The expression of the
p53 gene is to prevent cell death by repairing cells with UV damage. The
application of sunscreen diminishes the expression of p53; the cells are not
exposed to damaging ultraviolet radiation. Therefore, the expression of the
gene is not needed to prevent cell death of normal healthy skin cells.
The study also displayed at day 14
there was an increased amount of melanocytes after SSUVR exposure when compared
with sunscreen. According to the article the increased melanocytes increased
the pigmentation of the skin and helps prevent against induced DNA damage. The
results are significant and display the effectiveness of sunscreen. The
application of sunscreen is imperative to prevent molecular changes in skin
cells associated with skin cancer.
References
Yamaguchi, Y., Coelho, S.G., Zmudzka, B.Z., Takahashi, K., Beer,
J.Z., Hearing, V.J., and Miller, S.A. (2008). Cyclobutane pyrimidine dimer
formation and p53 production in human skin after repeated UV irradiation. Exp.
Dermatol. 17, 916–924.
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