Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14

被引:3
|
作者
Boehm, Malte [1 ]
Maier, Christiane [2 ]
Kuefer, Rainer [3 ]
Roepke, Albrecht [4 ,5 ]
Vogel, Walther [2 ]
Wieland, Ilse [5 ]
机构
[1] Otto Von Guericke Univ, Urol Klin, DE-39120 Magdeburg, Germany
[2] Univ Ulm, Inst Humangenet, D-89069 Ulm, Germany
[3] Univ Ulm, Urol Klin, D-89069 Ulm, Germany
[4] Univ Munster, Inst Humangenet, D-48149 Munster, Germany
[5] Otto Von Guericke Univ, Inst Humangenet, DE-39120 Magdeburg, Germany
关键词
Prostate cancer-susceptibility; DICE1/INTS6; 13q14.3; TUMOR-SUPPRESSOR GENE; SUSCEPTIBILITY GENES; DICE1; CARCINOMA; MUTATIONS; CELLS;
D O I
10.1159/000366229
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Prostate cancer is the most frequent malignancy found to occur in Caucasian men, but its genetic basis remains elusive. A prostate cancer-susceptibility locus has been identified on chromosome 13q14. The tumour suppressor gene deleted in cancer cells 1 (DICE1/INTS6) is located within this interval on 13q14.3. Materials and Methods: We performed mutation analysis of the DICE1/INTS6 gene in thirteen German prostate cancer families. Results and Conclusion: None of the patients harboured DICE1 mutations, and similar frequencies of the previously identified 13 bp deletion polymorphism in the DICE1 promoter were observed in the familial prostate cancer patients as compared with sporadic prostate cancer patients and controls. However, in one family with three affected brothers, the variations c.1215A>C (p.T405T) in exon 10 and c.2568A>G (p.S856S) in exon 17 were detected in a heterozygous pattern. In sporadic prostate cancer patients, variant c.2568A>G (p.S856S) was detected in 10/325 (3.08%) compared with 5/207 (2.42%) control samples (p > 0.05). We conclude that DICE1 appears to be involved in prostate cancer progression rather than in the initiation of prostate cancer. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:386 / 389
页数:4
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