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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Published inOncology letters Vol. 18; no. 4; pp. 4337 - 4345
Main Authors Lee, Sang Su, Min, Hyeonji, Ha, Ji Yong, Kim, Byung Hoon, Choi, Mi Sun, Kim, Shin
Format Journal Article
LanguageEnglish
Published Greece Spandidos Publications 01.10.2019
Spandidos Publications UK Ltd
D.A. Spandidos
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Abstract 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.
AbstractList 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.
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, DICER1, DROSHA, DiGeroge syndrome critical region gene 8 (DGCR8), and Argonaute 2 (AGO2), 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 DICER1, DROSHA, and DGCR8 were significantly decreased in both cohorts. However, AGO2 was significantly downregulated only in the Korean ccRCC cohort. Additionally, positive correlations were observed between the altered mRNA levels of DICER1 and DROSHA as well as DROSHA and DGCR8 in both cohorts. In the TCGA KIRC cohort, alterations in the mRNA levels of DICER1 were significantly correlated with histological grade. Furthermore, the altered mRNA levels of DGCR8 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 DICER1, DROSHA, DGCR8 and AGO2 are significantly dysregulated in ccRCC, suggesting that they are important in the pathophysiology of this malignancy.
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, D1CER1, DROSHA, DiGeroge syndrome critical region gene 8 (DGCR8), and Argonaute 2 (AGO2), 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 D1CER1, DROSHA, and DGCR8 were significantly decreased in both cohorts. However, AGO2 was significantly downregulated only in the Korean ccRCC cohort. Additionally, positive correlations were observed between the altered mRNA levels of D1CER1 and DROSHA as well as DROSHA and DGCR8 in both cohorts. In the TCGA KIRC cohort, alterations in the mRNA levels of DICER1 were significantly correlated with histological grade. Furthermore, the altered mRNA levels of DGCR8 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 DICER1, DROSHA, DGCR8 and AGO2 are significantly dysregulated in ccRCC, suggesting that they are important in the pathophysiology of this malignancy.
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, DICER1, DROSHA , DiGeroge syndrome critical region gene 8 ( DGCR8 ), and Argonaute 2 ( AGO2 ), 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 DICER1, DROSHA , and DGCR8 were significantly decreased in both cohorts. However, AGO2 was significantly downregulated only in the Korean ccRCC cohort. Additionally, positive correlations were observed between the altered mRNA levels of DICER1 and DROSHA as well as DROSHA and DGCR8 in both cohorts. In the TCGA KIRC cohort, alterations in the mRNA levels of DICER1 were significantly correlated with histological grade. Furthermore, the altered mRNA levels of DGCR8 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 DICER1, DROSHA, DGCR8 and AGO2 are significantly dysregulated in ccRCC, suggesting that they are important in the pathophysiology of this malignancy.
Audience Academic
Author Lee, Sang Su
Choi, Mi Sun
Kim, Shin
Min, Hyeonji
Kim, Byung Hoon
Ha, Ji Yong
AuthorAffiliation 2 Department of Immunology, School of Medicine, Keimyung University, Dalseo-gu, Daegu 42601, Republic of Korea
1 Department of Internal Medicine, Dongsan Medical Center, Keimyung University, Jung-gu, Daegu 41931, Republic of Korea
3 Department of Urology, Dongsan Medical Center, Keimyung University, Jung-gu, Daegu 41931, Republic of Korea
4 Department of Pathology, School of Medicine, Keimyung University, Dalseo-gu, Daegu 42601, Republic of Korea
AuthorAffiliation_xml – name: 1 Department of Internal Medicine, Dongsan Medical Center, Keimyung University, Jung-gu, Daegu 41931, Republic of Korea
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Snippet 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...
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StartPage 4337
SubjectTerms Biosynthesis
Cancer
Cancer genetics
Carcinoma
Cluster analysis
Colorectal cancer
Datasets
Gene expression
Genes
Genetic aspects
Genomes
Genomics
Kidney cancer
Messenger RNA
Metastasis
MicroRNA
MicroRNAs
Oncology
Professional associations
Renal cell carcinoma
RNA
Statistical analysis
Surgery
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Title 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
URI https://www.ncbi.nlm.nih.gov/pubmed/31516620
https://www.proquest.com/docview/2299077717
https://search.proquest.com/docview/2290856606
https://pubmed.ncbi.nlm.nih.gov/PMC6732956
Volume 18
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