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UVA radiation damages DNA in human melanocyte skin cells and can lead to melanoma

Date:
July 2, 2010
Source:
NYU Langone Medical Center / New York University School of Medicine
Summary:
A new study has found that UVA radiation damages the DNA in human melanocyte cells, causing mutations that can lead to melanoma. Melanocytes, which contain a substance called melanin that darkens the skin to protect it from the ultraviolet rays of the sun, are more vulnerable to UVA radiation than normal skin cells because they are unable to repair themselves as efficiently.

A new study by researchers at NYU School of Medicine found that UVA radiation damages the DNA in human melanocyte cells, causing mutations that can lead to melanoma. Melanocytes, which contain a substance called melanin that darkens the skin to protect it from the ultraviolet rays of the sun, are more vulnerable to UVA radiation than normal skin cells because they are unable to repair themselves as efficiently.

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"For the first time, UVA rays have been shown to cause significant damage to the DNA of human melanocyte skin cells," says Moon-shong Tang, PhD, professor of environmental medicine, pathology and medicine at NYU School of Medicine. "And because melanocytes have a reduced capacity to repair DNA damage from UVA radiation, they mutate more frequently, potentially leading to the development of melanoma."

In this study, researchers exposed lightly and darkly pigmented human melanocytes to UVA radiation and assessed DNA damage and the capacity of these cells to repair damaged DNA. DNA damage was detected in all melanocyte cells and these cells were unable to repair the damage. Normal skin cells were also exposed to UVA light but no damage to their DNA was observed.

"Identifying the underlying causes of melanoma allows researchers to develop new ways to assess a person's risk of melanoma, prevent the disease and aid in the design of more effective treatments," said Dr. Tang, who is also a member of the NYU Cancer Institute.

Sunlight in the form of UVA radiation causes oxygen in melanocytes to damage DNA. Thus, oxidative DNA damage adversely affects transcription and DNA replication in melanocytes. The authors concluded that UVA-induced oxidative DNA damage in melanocytes and the inherently reduced repair capacity in these cells are the two key factors that contribute to melanoma on the skin.

The authors also discovered the underlying mechanism to explain why melanoma can also develop in areas never exposed to sunlight: Because melanocytes generally have a limited capacity to repair any DNA damage, they have a higher mutation frequency rate and are more susceptible to the development of melanoma -- even without the effects of the sun.

"Melanoma, the deadliest form of skin cancer, continues to increase at a rate of 3 percent a year," says Dr. Tang. "This research highlights the necessity of limiting UVA radiation by avoiding excessive sunlight, tanning and sunbeds."

The study received funding from the National Institutes of Health in Bethesda, Maryland. It was published early online and will be appear in the print edition of the Proceedings of the National Academy of Sciences on July 6, 2010.


Story Source:

The above story is based on materials provided by NYU Langone Medical Center / New York University School of Medicine. Note: Materials may be edited for content and length.


Cite This Page:

NYU Langone Medical Center / New York University School of Medicine. "UVA radiation damages DNA in human melanocyte skin cells and can lead to melanoma." ScienceDaily. ScienceDaily, 2 July 2010. <www.sciencedaily.com/releases/2010/07/100701103415.htm>.
NYU Langone Medical Center / New York University School of Medicine. (2010, July 2). UVA radiation damages DNA in human melanocyte skin cells and can lead to melanoma. ScienceDaily. Retrieved December 21, 2014 from www.sciencedaily.com/releases/2010/07/100701103415.htm
NYU Langone Medical Center / New York University School of Medicine. "UVA radiation damages DNA in human melanocyte skin cells and can lead to melanoma." ScienceDaily. www.sciencedaily.com/releases/2010/07/100701103415.htm (accessed December 21, 2014).

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