Literature DB >> 19711014

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

Nives Pećina-Slaus1, Zeljka Majić, Vesna Musani, Martina Zeljko, Hrvoje Cupić.   

Abstract

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.

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Year:  2009        PMID: 19711014     DOI: 10.1007/s11060-009-0001-7

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  25 in total

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2.  Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.

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9.  Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.

Authors:  R J Scott; R van der Luijt; M Spycher; J L Mary; A Müller; T Hoppeler; M Haner; H Müller; S Martinoli; P L Brazzola
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  8 in total

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