VYCHYTILOVÁ, Petra, Alena KOVAŘÍKOVÁ, Marek SVOBODA, Rostislav VYZULA a Ondřej SLABÝ. Genes of the microRNA biogenesis pathway are deregulated in colorectal cancer. In The Non-Coding Genome, Heidelberg, Germany. 2013.
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Základní údaje
Originální název Genes of the microRNA biogenesis pathway are deregulated in colorectal cancer
Autoři VYCHYTILOVÁ, Petra (203 Česká republika, domácí), Alena KOVAŘÍKOVÁ (203 Česká republika, domácí), Marek SVOBODA (203 Česká republika), Rostislav VYZULA (203 Česká republika) a Ondřej SLABÝ (203 Česká republika, garant, domácí).
Vydání The Non-Coding Genome, Heidelberg, Germany, 2013.
Další údaje
Originální jazyk angličtina
Typ výsledku Konferenční abstrakt
Obor 30200 3.2 Clinical medicine
Stát vydavatele Německo
Utajení není předmětem státního či obchodního tajemství
Kód RIV RIV/00216224:14740/13:00065633
Organizační jednotka Středoevropský technologický institut
Klíčová slova anglicky colorectal cancer; miRNA biogenesis; biomarkers; therapeutic targets
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Petra Vychytilová, Ph.D., učo 211789. Změněno: 22. 1. 2014 12:09.
Anotace
MicroRNAs (miRNAs) are small non-coding RNAs 18-25 nucleotides long that regulate gene expression on post-transcriptional level. Therefore, their production and maturation have to be strictly regulated. Their biogenesis starts with the transcription, which is followed by several steps that lead to processing of primary transcripts to mature miRNAs. Each step of this pathway is sophistically regulated and any disruption of control mechanisms may leads to the cancer occurrence. The aim of this study was to analyse the expression of the crucial genes involved in the biogenesis of miRNAs in colorectal cancer (CRC). Expression of 19 selected genes (EIF2C1-4, GEMIN4, DDX20, TARBP2, DICER1, XPO5, DROSHA, DGCR8, POLR2A, DDX5, DDX17, ADAR, ADARB1, TNRC6A, LIN28A/B) has been analysed in tumour tissues of 120 clinically characterized patients with CRC and in 120 parallel healthy tissues by qRT-PCR. Using Wilcoxon test, genes with different expression between tumour tissue and healthy tissue have been identified. Subsequently, Kruskal-Wallis test has been used to find any correlation with the clinical-pathological features of the patients. We have found significantly higher expression of POLRIIA, ADAR, ADARB1, DGCR8, DDX5, DDX17, DROSHA, XPO5, EIF2C1-C4, TARBP2, TNRC6A, GEMIN3, DDX20 and DICER1 (P < 0.0001) and significantly lower expression of LIN28A in tumour tissue of CRC patients. Moreover, negative correlation between the expression of AGO3 and clinical stage of patients (P = 0.0017) and grade (P = 0.0151) and positive correlation between the expression of DICER1 (P = 0.0230) and DROSHA (P = 0.0212) and grade of patients has been observed. Our results show that changes in the expression of genes associated with biogenesis of miRNAs may be associated not only with the origin, but also to progression of CRC and therefore, these molecules could serve as potential new biomarkers or therapeutic targets.
Návaznosti
NT13549, projekt VaVNázev: Vytvoření diagnostické sady cirkulujících mikroRNA pro neinvazivní časnou diagnostiku a sledování pacientů s kolorektálním karcinomem
VytisknoutZobrazeno: 26. 7. 2024 19:37