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izvor podataka: crosbi

Frequency of loss of heterozygosity of the NF2 gene in schwannomas from Croatian patients (CROSBI ID 186190)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Pećina-Šlaus, Nives ; Zeljko, Martina ; Pećina, Hrvoje Ivan ; Nikuševa Martić, Tamara ; Bačić, Niko ; Tomas, Davor ; Hrašćan, Reno Frequency of loss of heterozygosity of the NF2 gene in schwannomas from Croatian patients // Croatian medical journal, 53 (2012), 4; 321-327. doi: 10.3325/cmj.2012.53.321

Podaci o odgovornosti

Pećina-Šlaus, Nives ; Zeljko, Martina ; Pećina, Hrvoje Ivan ; Nikuševa Martić, Tamara ; Bačić, Niko ; Tomas, Davor ; Hrašćan, Reno

engleski

Frequency of loss of heterozygosity of the NF2 gene in schwannomas from Croatian patients

Aim was to identify gross deletions in the NF2 gene in a panel of schwannomas from Croatian patients in order to establish their frequencies in Croatian population. Changes of the NF2 gene were tested by polymerase chain reaction/loss of heterozygosity (LOH) using two microsatellite markers, D22S444 and D22S929. The analysis with both markers demonstrated that 43.75% of schwannomas exhibited LOH of the NF2 gene. The D22S444 region exhibited 45.5% of LOHs and the D22S929 region exhibited 14.3% of LOHs. Four LOHs were found in Antoni B, 2 in Antoni A, and 1 in Antoni A and B type tumors. The frequency of changes observed in Croatian patients is broadly similar to that reported in other populations and thus confirms the existing hypothesis regarding the tumorigenesis of schwannomas and contributes to schwannoma genetic profile helping us to better understand its etiology and treatment.

NF2; schwannoma

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Podaci o izdanju

53 (4)

2012.

321-327

objavljeno

0353-9504

10.3325/cmj.2012.53.321

Povezanost rada

Temeljne medicinske znanosti, Biotehnologija

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