2019
The detection of DNA methylation of tumour suppressor genes in cervical high-grade squamous intraepithelial lesion: A prospective cytological-histological correlation study of 70 cases
ONDIČ, Ondrej, Jana NĚMCOVÁ, Reza ALAGHEHBANDAN, Kateřina ČERNÁ, Barbora GOMOLČÁKOVÁ et. al.Základní údaje
Originální název
The detection of DNA methylation of tumour suppressor genes in cervical high-grade squamous intraepithelial lesion: A prospective cytological-histological correlation study of 70 cases
Autoři
ONDIČ, Ondrej (203 Česká republika, garant), Jana NĚMCOVÁ (203 Česká republika), Reza ALAGHEHBANDAN (124 Kanada), Kateřina ČERNÁ (203 Česká republika), Barbora GOMOLČÁKOVÁ (203 Česká republika), Iva KINKOROVÁ-LUŇÁČKOVÁ (203 Česká republika), Jan CHYTRA (203 Česká republika), Henrieta ŠIDLOVÁ (703 Slovensko), Ondřej MÁJEK (203 Česká republika, domácí) a Jiří BOUDA (203 Česká republika)
Vydání
CYTOPATHOLOGY, HOBOKEN, WILEY, 2019, 0956-5507
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 1.493
Kód RIV
RIV/00216224:14110/19:00110577
Organizační jednotka
Lékařská fakulta
UT WoS
000472237900011
Klíčová slova anglicky
cervix; cytology; HSIL; hypermethylation; methylation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 9. 2019 15:18, Mgr. Tereza Miškechová
Anotace
V originále
Background DNA methylation has been suggested as one of the epigenetic changes promoting carcinogenesis. The aim of this study was to prospectively evaluate the methylation status of CADM 1, MAL and hsa-miR-124 genes in high-grade squamous intraepithelial lesion (HSIL) liquid-based cytology (LBC) samples with a histological correlation. Methods Seventy histologically confirmed cases of HSIL paired with prior screening LBC diagnosis of HSIL within a 3-month interval were selected. Histologically, the lesions were reviewed and assessed including: (a) number of blocks harbouring dysplastic squamous epithelium; (b) number of blocks containing glandular extension of dysplastic epithelium; and (c) the depth of glandular extension (which was assessed semi-quantitatively as graded 1-3). Human papillomavirus (HPV) subtyping was performed from residual LBC materials using the LINEAR ARRAY HPV Genotyping Test and in-house polymerase chain reaction targeting the HPV E1 gene. The detection of methylation silencing of tumour suppressor genes CADM1, MAL and hsa-miR-124 was performed by multiplex methylation-specific real-time polymerase chain reaction. Results A positive methylation status was detected in 41 cases (58.6%). The number of blocks with HSIL varied from one to 13. Glandular extension was seen in 44 cases with the number of blocks involved ranging from one to 10. The depth of HSIL glandular extension varied. Conclusion The DNA methylation test allows HSIL lesions to be divided into two distinct groups of methylated HSIL in significantly older patients and unmethylated HSIL in younger patients. This study was not able to prove that methylation status in cervical HSIL correlates with the size of the lesion (measured by the number of blocks involved) or with HSIL propensity for endocervical glandular extension, nor with HPV type or multi-infection.