Napredna pretraga

Pregled bibliografske jedinice broj: 900217

Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite


Pećina-Šlaus, Nives; Kafka, Anja; Bukovac, Anja; Vladušić, Tomislav; Tomas, Davor; Hrašćan, Reno
Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite // Tumor biology, 39 (2017), 7; 1-9 doi:10.1177/1010428317705791 (međunarodna recenzija, članak, znanstveni)


Naslov
Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite
(Genetic changes of MLH1 and MSH2 genes could explain constant findings on microsatellite instability in intracranial meningioma)

Autori
Pećina-Šlaus, Nives ; Kafka, Anja ; Bukovac, Anja ; Vladušić, Tomislav ; Tomas, Davor ; Hrašćan, Reno

Izvornik
Tumor biology (1010-4283) 39 (2017), 7; 1-9

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Meningioma, microsatellite instability, loss of heterozygosity, MLH1 MSH2, BAT26, D3S1611, AXIN1, CDH1, DVL3

Sažetak
Postreplicative mismatch repair safeguards the stability of our genome. The defects in its functioning will give rise to microsatellite instability. In this study, 50 meningiomas were investigated for microsatellite instability. Two major mismatch repair genes, MLH1 and MSH2, were analyzed using microsatellite markers D1S1611 and BAT26 amplified by polymerase chain reaction and visualized by gel electrophoresis on high-resolution gels. Furthermore, genes DVL3 (D3S1262), AXIN1 (D16S3399), and CDH1 (D16S752) were also investigated for microsatellite instability. Our study revealed constant presence of microsatellite instability in meningioma patients when compared to their autologous blood DNA. Altogether 38% of meningiomas showed microsatellite instability at one microsatellite locus, 16% on two, and 13.3% on three loci. The percent of detected microsatellite instability for MSH2 gene was 14%, and for MLH1, it was 26%, for DVL3 22.9%, for AXIN1 17.8%, and for CDH1 8.3%. Since markers also allowed for the detection of loss of heterozygosity, gross deletions of MLH1 gene were found in 24% of meningiomas. Genetic changes between MLH1 and MSH2 were significantly positively correlated (p = 0.032). We also noted a positive correlation between genetic changes of MSH2 and DVL3 genes (p = 0.034). No significant associations were observed when MLH1 or MSH2 was tested against specific histopathological meningioma subtype or World Health Organization grade. However, genetic changes in DVL3 were strongly associated with anaplastic histology of meningioma (χ2 = 9.14 ; p = 0.01). Our study contributes to better understanding of the genetic profile of human intracranial meningiomas and suggests that meningiomas harbor defective cellular DNA mismatch repair mechanisms.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekt / tema
HRZZ 6625

Ustanove
Prehrambeno-biotehnološki fakultet, Zagreb,
Medicinski fakultet, Zagreb,
KBC "Sestre Milosrdnice"

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati