Telomerase promoter mutations in human immunodeficiency virus-related conjunctiva neoplasia

被引:8
|
作者
Starita, Noemy [1 ]
Buonaguro, Luigi [1 ]
Buonaguro, Franco M. [1 ]
Tornesello, Maria Lina [1 ]
机构
[1] Ist Nazl Tumori IRCCS Fdn G Pascale, Mol Biol & Viral Oncol Unit, Via Mariano Semmola, I-80131 Naples, Italy
来源
JOURNAL OF TRANSLATIONAL MEDICINE | 2018年 / 16卷
关键词
TERT promoter; Mutations; Conjunctiva neoplasia; Kaposi sarcoma; HIV; Africa; SQUAMOUS-CELL CARCINOMA; TERT PROMOTER; SKIN-CANCER; TP53; MUTATIONS; HIV-INFECTION; AIDS; EPIDEMIOLOGY; PATTERN; PATIENT; GLIOMAS;
D O I
10.1186/s12967-018-1456-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Squamous cell carcinoma (SCC) of the conjunctiva is a common cancer in Africa mainly associated with solar ultraviolet (UV) exposure and human immunodeficiency virus (HIV) infection. We analyzed the role of HIV on the occurrence of telomerase reverse transcriptase (TERT) promoter mutations among a cohort of conjunctiva neoplasia Ugandan patients. Methods: Telomerase reverse transcriptase promoter mutations were searched in 72 conjunctiva neoplasia cases, comprising SCC and intraepithelial neoplasia grade 1-3 (CIN1-3), as well as in 53 conjunctiva normal tissues and in 24 HIV-related Kaposi sarcoma. Results: The average prevalence of TERT promoter mutations in conjunctiva neoplasia was 31.9%. The mutation rates were significantly higher in HIV-positive (31.8% of CIN1 and CIN2, 46.2% of CIN3 and SCC,) than HIV-negative patients (22.2% of CIN1 and CIN2, 13.3% of CIN3 and SCC). Such mutations were rarely identified among HIV-positive conjunctiva controls (3.6%) and never in Kaposi sarcoma lesions. The most frequent variations were the hot spots - 124G>A and - 146G>A and tandem transitions - 124_125GG>AA and -138_139GG>AA. Conclusions: Telomerase reverse transcriptase promoter mutations are early events in conjunctival neoplasia and could be used for timely diagnosis of conjunctiva tumours. The high frequency of UV-signatures in HIV-positive conjunctiva lesions suggests an additive effect of the virus to UV-related mutagenesis.
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页数:7
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