Dysregulation of the miRNA biogenesis components DICER1, DROSHA, DGCR8 and AGO2 in clear cell renal cell carcinoma in both a Korean cohort and the cancer genome atlas kidney clear cell carcinoma cohort
Impairment of microRNA (miRNA) biogenesis may be involved in clear cell renal cell carcinoma (ccRCC). The objective of the present study was to investigate the mRNA levels of important miRNA machinery components, , DiGeroge syndrome critical region gene 8 ( ), and Argonaute 2 ( ), and their correlat...
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Veröffentlicht in: | Oncology letters 2019-10, Vol.18 (4), p.4337-4345 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Impairment of microRNA (miRNA) biogenesis may be involved in clear cell renal cell carcinoma (ccRCC). The objective of the present study was to investigate the mRNA levels of important miRNA machinery components,
, DiGeroge syndrome critical region gene 8 (
), and Argonaute 2 (
), and their correlations with clinicopathological characteristics of ccRCC using mRNA expression data from The Cancer Genome Atlas kidney clear cell carcinoma (TCGA KIRC) cohort and a Korean ccRCC cohort. mRNA levels of
, and
were significantly decreased in both cohorts. However,
was significantly downregulated only in the Korean ccRCC cohort. Additionally, positive correlations were observed between the altered mRNA levels of
and
as well as
and
in both cohorts. In the TCGA KIRC cohort, alterations in the mRNA levels of
were significantly correlated with histological grade. Furthermore, the altered mRNA levels of
showed significant associations with sex and histologic grades. However, in the Korean ccRCC cohort, no factors were significantly associated with any clinicopathological parameters, including sex, age, T stage, Fuhrman grade/The International Society of Urological Pathology grade, lymphovascular invasion, and peri-renal fat invasion. Taken together, these findings indicate that
and
are significantly dysregulated in ccRCC, suggesting that they are important in the pathophysiology of this malignancy. |
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ISSN: | 1792-1074 1792-1082 |
DOI: | 10.3892/ol.2019.10759 |