Low frequency of microsatellite instability in hereditary prostate cancer

被引:14
作者
Åhman, AK
Jonsson, BA
Damber, JE
Bergh, A
Grönberg, H [1 ]
机构
[1] Umea Univ, Dept Radiat Sci, S-90187 Umea, Sweden
[2] Umea Univ, Dept Pathol, S-90187 Umea, Sweden
[3] Sahlgrens Univ Hosp, Inst Surg Sci, Dept Urol, S-41345 Gothenburg, Sweden
关键词
hereditary prostate cancer; microsatellite instability; replication error; genetics; prostate cancer;
D O I
10.1046/j.1464-410x.2001.00104.x
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
Objective To investigate whether there is widespread microsatellite instability (MSI) in families with hereditary prostate cancer (HPC). Patients and methods Eighty-four prostate tumours from 80 Swedish men in 35 families with HPC were screened for genetic instability at microsatellite marker loci BAT-25, BAT-26, BAT-34C4, D2S123 and D17S250. Results MSI was detected in only five individuals from different families. Three tumours (4%) were unstable at more than two MSI loci and hence classified high-frequency MSI (MSI-H) according to a previous definition, Interestingly, two of the MSI-H tumours were from patients in families with both HPC and familial colon cancer. Conclusions Widespread MSI is a rare event in hereditary prostate cancer, indicating that defective DNA mismatch repair is not an important element in the genesis of HPC.
引用
收藏
页码:334 / 338
页数:5
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