TERT rs2736100 genotypes are associated with differential risk of myeloproliferative neoplasms in Swedish and Chinese male patient populations

被引:27
作者
Dahlstrom, Jenny [1 ,2 ]
Liu, Tiantian [3 ]
Yuan, Xiaotian [1 ,2 ]
Saft, Leonie [4 ]
Ghaderi, Mehran [4 ]
Wei, Ya Bin [5 ]
Lavebratt, Catharina [5 ]
Li, Ping [6 ]
Zheng, Chengyun [7 ]
Bjorkholm, Magnus [1 ,2 ]
Xu, Dawei [1 ,2 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp Solna, Dept Med, Div Hematol, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Karolinska Univ Hosp Solna, Ctr Mol Med, S-17177 Stockholm, Sweden
[3] Shandong Univ, Sch Med, Dept Pathol, Jinan, Peoples R China
[4] Karolinska Inst, Dept Pathol & Oncol, Stockholm, Sweden
[5] Karolinska Inst, Dept Mol Med & Surg, Neurogenet Unit, Stockholm, Sweden
[6] Shandong Univ, Sch Nursing, Jinan, Peoples R China
[7] Shandong Univ, Hosp 2, Dept Hematol, Jinan, Peoples R China
基金
瑞典研究理事会; 中国国家自然科学基金;
关键词
Telomerase; Myeloproliferative neoplasms; Cancer genetics; Single nucleotide polymorphism; TERT; TELOMERE LENGTH; POLYMORPHISM; CANCER; LOCUS; JAK2; TRANSFORMATION; CONTRIBUTES; MUTATIONS; VARIANTS; THERAPY;
D O I
10.1007/s00277-016-2787-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The telomerase reverse transcriptase (TERT) gene rs2736100_C allele has recently been shown to be associated with an increased risk for myeloproliferative neoplasms (MPNs) among Caucasians. However, it is unknown if this association is present in other ethnical populations and whether rs2736100 allele frequencies mirror the incidence of MPNs in a population. Here we genotyped TERT rs2736100 variants in 126 Swedish and 101 Chinese MPN patients and their age-, sex-, and ethnically-matched healthy controls. Healthy Chinese adults had a higher frequency of the A allele and lower frequencies of the C allele compared to Swedish counterparts (57.4 vs 47.0 % for A, 42.6 vs 53.0 % for C, P = 0.006). Both Swedish and Chinese patients harbored significantly higher C allele frequency than their controls (62.7 vs 53.0 % and 57.4 vs 42.6 % for Swedish and Chinese, respectively, P = 0.004). Swedes and Chinese bearing the CC genotype had a significantly increased risk of MPN compared to AA carriers (OR = 2.47; 95 % CI: 1.33-4.57, P = 0.003, for Swedes, and OR = 3.45; 95 % CI: 1.52-7.85, P = 0.005, for Chinese). Further analyses showed that rs2736100_CC was associated with robustly enhanced risk in males only (CC vs AA, OR = 5.11; 95 % CI: 2.19-11.92, P < 0.0001). The CC-carryingMPN patients exhibited significantly higher TERT expression than patients with the AC genotype. Collectively, the rs2736100_C is a risk allele for MPNs in Swedish and Chinese males, and the lower incidence of MPNs in the Chinese population is correlated with a lower rs2736100_C risk allele frequency.
引用
收藏
页码:1825 / 1832
页数:8
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