Australian researchers find unexpected genomic landscape in melanoma
Genetic changes in acral and mucosal melanomas are completely different to the mutations found in skin melanoma, reveals a new study by Australian researchers.
The findings by researchers at Melanoma Institute Australia, QIMR Berghofer Medical Research Institute and The University of Sydney confirm melanomas on the hands and feet (acral) and internal surfaces (mucosal), and skin melanomas as very distinct diseases.
“Our study has provided a whole series of observations and important new insights from whole genome sequencing, some of which you would expect but others which are quite surprising,” said Professor Richard Scolyer, Conjoint Medical Director of Melanoma Institute Australia and a lead author.
The findings of the “largest gene-sequencing study ever undertaken in melanoma, and one of the biggest in the field of oncology — as part of the Australian Melanoma Genome Project” were published in Nature. This is the first large study to survey the entire DNA sequence of melanomas, giving 50 times more information than most previous work which has focused on the coding regions of genes, according to the researchers. Many genes were found to have damaged control mechanisms and may be previously unsuspected drivers of melanoma.
UV radiation does not cause acral or mucosal melanoma, the researchers discovered. Using whole-genome sequencing on tumours from 183 patients, the study found genetic mutations caused by ultraviolet (UV) radiation were dominant in skin melanoma, whereas complex structural rearrangements not caused by UV radiation dominated in acral and mucosal melanoma. In fact, none of the other known genetic signatures for environmental causes of cancer matched with what was seen in acral and mucosal melanoma.
“We know that sun protection works to prevent skin melanoma, but it’s not going to get these other forms of melanoma under control,” said Professor Nicholas Hayward, a lead author from QIMR Berghofer Medical Research Institute.
These findings show that not only do acral and mucosal melanoma have different causes to skin melanoma, but they explain why new therapies that have been so successful in treating skin melanoma have been less unsuccessful in treating acral and mucosal melanoma.
New driver mutations identified
By studying the whole genome, researchers have identified a number of new uncommon driver mutations in skin melanoma and confirmed the importance of other major mutations driving melanoma.
“We did not see any melanoma driver mutations that were as common as the ones we already knew about, such as BRAF. This is an important negative finding,” commented Professor Graham Mann, a lead author at Melanoma Institute Australia. “However, we have shown for the first time that melanomas carry a wide range of mutations in gene control mechanisms, and some of these are very likely to be drivers.
“We overcame important technical difficulties to find this out. Skin melanoma is riddled with mutations because the sun is so effective at damaging genes. That creates a lot of noise and makes it challenging to find the wood for the trees.” The researchers engaged a team, led by Professor Núria López-Bigas from the Institute for Research in Biomedicine and Pompeu Fabra University, Barcelona, which is expert in separating this genomic noise. They applied a new technique to the melanoma genome data to correctly identify which mutations are most important, and therefore which genes are the most promising targets for therapy.
Mucosal melanoma genetically similar to eye melanoma
Although there are fewer genetic mutations in mucosal melanoma compared to skin melanoma, the research identified specific driver mutations (SF3B1 and GNAQ genes) that are similar to those found in eye (uveal) melanoma. This could have important outcomes for therapeutic development and helps explain why treatments that often work in skin melanoma are often ineffective in uveal, acral and mucosal melanoma.
A paradoxical relationship between mutations to the telomerase enzyme and telomere length was observed, which may help unravel our understanding of the relationship of these mutations in tumour development. Cells that have to live a long time have to be able to continuously repair and maintain their telomeres. A key genetic mutation previously observed in most melanoma over-activates the telomerase gene, so it was expected that longer telomeres would be found in these melanoma cells.
However, the study found this mutation produced telomeres that were actually shorter than average. “This is a surprising finding that opens the door to further enquiry,” said Professor Mann.
“It means that there is something else going on; telomerase must control the way telomere length is regulated rather than just make telomeres longer.
“This finding challenges and adds to our fundamental understanding of telomerase and the role it plays in melanoma and indeed all cancer.”
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