Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations
Burke, Laura S.
Hyland, Paula L.
Pfeiffer, Ruth M.
Savage, Sharon A.
Tucker, Margaret A.
Goldstein, Alisa M.
Yang, Xiaohong R.Note: Order does not necessarily reflect citation order of authors.
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CitationBurke, L. S., P. L. Hyland, R. M. Pfeiffer, J. Prescott, W. Wheeler, L. Mirabello, S. A. Savage, et al. 2013. “Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations.” PLoS ONE 8 (8): e71121. doi:10.1371/journal.pone.0071121. http://dx.doi.org/10.1371/journal.pone.0071121.
AbstractIntroduction: Recent evidence suggests a link between constitutional telomere length (TL) and cancer risk. Previous studies have suggested that longer telomeres were associated with an increased risk of melanoma and larger size and number of nevi. The goal of this study was to examine whether TL modified the risk of melanoma in melanoma-prone families with and without CDKN2A germline mutations. Materials and Methods We measured TL in blood DNA in 119 cutaneous malignant melanoma (CMM) cases and 208 unaffected individuals. We also genotyped 13 tagging SNPs in TERT. Results: We found that longer telomeres were associated with an increased risk of CMM (adjusted OR = 2.81, 95% CI = 1.02–7.72, P = 0.04). The association of longer TL with CMM risk was seen in CDKN2A- cases but not in CDKN2A+ cases. Among CMM cases, the presence of solar injury was associated with shorter telomeres (P = 0.002). One SNP in TERT, rs2735940, was significantly associated with TL (P = 0.002) after Bonferroni correction. Discussion Our findings suggest that TL regulation could be variable by CDKN2A mutation status, sun exposure, and pigmentation phenotype. Therefore, TL measurement alone may not be a good marker for predicting CMM risk.
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