TERT Promoter Mutations in Skin Cancer: The Effects of Sun Exposure and X-Irradiation

被引:103
作者
Populo, Helena [1 ]
Boaventura, Paula [1 ]
Vinagre, Joao [1 ,2 ]
Batista, Rui [1 ]
Mendes, Adelia [1 ]
Caldas, Regina [3 ]
Pardal, Joana [4 ]
Azevedo, Filomena [5 ]
Honavar, Mrinalini [6 ]
Guimaraes, Isabel [7 ]
Lopes, Jose Manuel [1 ,3 ,4 ]
Sobrinho-Simoes, Manuel [1 ,3 ,4 ]
Soares, Paula [1 ,3 ]
机构
[1] Univ Porto IPATIMUP, Inst Mol Pathol & Immunol, Dept Canc Biol, P-4200465 Oporto, Portugal
[2] Univ Porto, Inst Biomed Sci Abel Salazar, P-4100 Oporto, Portugal
[3] Univ Porto, Fac Med, Dept Pathol & Oncol, P-4100 Oporto, Portugal
[4] Hosp Sao Joao, Dept Pathol, Oporto, Portugal
[5] Hosp Sao Joao, Dept Dermatol, Oporto, Portugal
[6] Hosp Pedro Hispano, Dept Pathol, Senhora Da Hora, Portugal
[7] Hosp Pedro Hispano, Dept Plast Surg, Senhora Da Hora, Portugal
关键词
BASAL-CELL CARCINOMA; HIGHLY RECURRENT; MTOR PATHWAY; CHILDHOOD; HEAD;
D O I
10.1038/jid.2014.163
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The reactivation or reexpression of telomerase (TERT) is a widespread feature of neoplasms. TERT promoter mutations were recently reported that were hypothesized to result from UV radiation. In this retrospective study, we assessed TERT promoter mutations in 196 cutaneous basal cell carcinomas (BCCs), including 102 tumors from X-irradiated patients, 94 tumors from patients never exposed to ionizing radiation treatment, and 116 melanomas. We sought to evaluate the effects of UV and X-ray irradiation on TERT mutation frequency. TERT mutations were detected in 27% of BCCs from X-irradiated patients, 51% of BCCs from nonirradiated patients, and 22% of melanoma patients. TERT mutations were significantly increased in non-X-irradiated BCC patients compared with X-irradiated BCC patients; the mutations also presented a different mutation signature. In nonirradiated patients, TERT mutations were more frequent in BCCs of sun-exposed skin, supporting a possible causative role of UV radiation. In melanoma, TERT promoter mutations were generally restricted to intermittent sun-exposed areas and were associated with nodular and superficial spreading subtypes, increased thickness, ulceration, increased mitotic rate, and BRAFV600E mutations. Our results suggest that various carcinogenic factors may cause distinct TERT promoter mutations in BCC and that TERT promoter mutations might be associated with a poorer prognosis in melanoma.
引用
收藏
页码:2251 / 2257
页数:7
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