2015
Evaluation of Cell-Free Urine microRNAs Expression for the Use in Diagnosis of Ovarian and Endometrial Cancers. A Pilot Study
ZÁVESKÝ, Luděk; Eva JANDÁKOVÁ; Radovan TURYNA; Lucie LANGMEIEROVÁ; Vít WEINBERGER et al.Základní údaje
Originální název
Evaluation of Cell-Free Urine microRNAs Expression for the Use in Diagnosis of Ovarian and Endometrial Cancers. A Pilot Study
Autoři
ZÁVESKÝ, Luděk; Eva JANDÁKOVÁ; Radovan TURYNA; Lucie LANGMEIEROVÁ; Vít WEINBERGER; Lenka ZÁVESKÁ DRÁBKOVÁ; Martina HŮLKOVÁ; Aleš HOŘÍNEK; Daniela DUŠKOVÁ; Jaroslav FEYEREISL; Luboš MINÁŘ a Milada KOHOUTOVÁ
Vydání
Pathology & Oncology Research, Dordrecht, Springer, 2015, 1219-4956
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30214 Obstetrics and gynaecology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 1.940
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/15:00083502
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
ovarian cancer; endometrial cancer; urine; microRNA;miR-92a; miR-106b
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 16. 12. 2015 17:04, Soňa Böhmová
Anotace
V originále
Among gynaecological cancers, epithelial ovarian cancers are the most deadly cancers while endometrial cancers are the most common diseases. Efforts to establish relevant novel diagnostic, screening and prognostic markers are aimed to help reduce the high level of mortality, chemoresistance and recurrence, particularly in ovarian cancer. MicroRNAs, the class of post-transcriptional regulators, have emerged as the promising diagnostic and prognostic markers associated with various diseased states recently. Urine has been shown as the source of microRNAs several years ago; however, there has been lack of information on urine microRNA expression in ovarian and endometrial cancers till now. In this pilot study, we examined the expression of candidate cell-free urine microRNAs in ovarian cancer and endometrial cancer patients using quantitative real-time PCR. We compared the expression between pre- and post-surgery ovarian cancer samples, and between patients with ovarian and endometrial cancers and healthy controls, within three types of experiments. These experiments evaluated three different isolation methods of urine RNA, representing two supernatant and one exosome fractions of extracellular microRNA. In ovarian cancer, we found miR-92a significantly up-regulated, and miR-106b significantly down-regulated in comparison with control samples. In endometrial cancer, only miR-106b was found down-regulated significantly compared to control samples. Using exosome RNA, no significant de-regulations in microRNAs expression could be found in either of the cancers investigated.We propose that more research should now focus on confirming the diagnostic potential of urine microRNAs in gynaecological cancers using more clinical samples and largescale expression profiling methods.