Pregled bibliografske jedinice broj: 428787
Report on mutation in exon 15 of the APC gene in a case of brain metastasis
Report on mutation in exon 15 of the APC gene in a case of brain metastasis // The third Croatian congress of neuroscience : Book of Abstracts / Šimić, Goran (ur.).
Zagreb: Hrvatsko društvo za neuroznanost, 2009. str. 57-57 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 428787 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Report on mutation in exon 15 of the APC gene in a case of brain metastasis
Autori
Pećina-Šlaus, Nives ; Majić, Željka ; Musani, Vesna ; Zeljko, Martina ; Čupić, Hrvoje
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The third Croatian congress of neuroscience : Book of Abstracts
/ Šimić, Goran - Zagreb : Hrvatsko društvo za neuroznanost, 2009, 57-57
Skup
Croatian congress of neuroscience (3 ; 2009)
Mjesto i datum
Zadar, Hrvatska, 24.09.2009. - 26.09.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Adenomatous polyposis coli gene; mutation; brain metastasis; G– A transversion
Sažetak
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.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1081870-1905 - Uloga signalnog puta wnt u tumorigenezi i embriogenezi mozga (Pećina-Šlaus, Nives, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb