Report on mutation in exon 15 of the APC gene in a case of brain metastasis

被引:12
|
作者
Pecina-Slaus, Nives [1 ,2 ]
Majic, Zeljka [1 ]
Musani, Vesna [3 ]
Zeljko, Martina [1 ]
Cupic, Hrvoje [4 ]
机构
[1] Univ Zagreb, Sch Med, Croatian Inst Brain Res, Lab Neurooncol, Zagreb 10000, Croatia
[2] Univ Zagreb, Sch Med, Dept Biol, Zagreb 10000, Croatia
[3] Rudjer Boskovic Inst, Lab Hereditary Canc, Div Mol Med, Zagreb 10000, Croatia
[4] Univ Hosp Sisters Char, Ljudevit Jurak Dept Pathol, Zagreb 10000, Croatia
关键词
Adenomatous polyposis coli gene; Mutation; Brain metastasis; G-A transversion; FAMILIAL ADENOMATOUS POLYPOSIS; CELL LUNG-CANCER; SOMATIC MUTATIONS; SILENT MUTATION; HETEROZYGOSITY; GERMLINE; PHENOTYPES; PATHWAYS; MISSENSE; NONSENSE;
D O I
10.1007/s11060-009-0001-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The study analyzes exon 15 of the adenomatous polyposis coli gene (APC) in a 49-year-old male patient with brain metastasis. The primary site was lung carcinoma. PCR method and direct DNA sequencing of the metastasis and autologous lymphocyte samples identified the presence of a somatic mutation. The substitution was at position 5883 G-A in the metastasis tissue. The mutation was confirmed by RFLP analysis using Msp I endonuclease, since the mutation strikes the Msp I restriction site. Immunohistochemical analysis revealed the lack of protein expression of this tumor suppressor gene. The main molecular activator of the wnt pathway, beta-catenin, was expressed, and located in the nucleus. The mutation is a silent mutation that might have consequences in the creation of a new splice site. Different single-base substitutions in APC exons need not only be evaluated by the predicted change in amino acid sequence, but rather at the nucleotide level itself. In our opinion, such silent mutations should also be incorporated in mutation detection rate and validation.
引用
收藏
页码:143 / 148
页数:6
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