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Published on: November 30, 2013
Aberrantly expressed microRNAs in bladder cancer and renal cell carcinoma
Akira Kurozumi1,2, Yusuke Goto1,2, Atsushi Okato1,2
1Department of Functional Genomics, Graduate School of Medicine, Chiba University, Chiba, Japan.
Abstract:
Bladder cancer (BC) and renal cell carcinoma (RCC) are frequently diagnosed urinary tract cancers. Recently developed molecular-targeted therapies for RCC have shown remarkable therapeutic efficacy; however, no targeted therapeutics are currently approved for the treatment of BC, and few effective treatment options exist. Current studies have shown that small noncoding RNA molecules have major roles in cancer cells. MicroRNAs (miRNAs) are endogenous small noncoding RNA molecules that regulate protein-/nonprotein-coding RNAs in human cells. A large body of evidence suggests that aberrantly expressed miRNAs are deeply involved in the pathogenesis of human cancers. In this paper, we review recently published miRNA expression signatures of BC and RCC. We focus on downregulated or upregulated miRNAs in multiple signatures and discuss putative target genes of miRNAs. Comparisons of RCC and BC expression signatures revealed that the two types of cancer showed opposite expression patterns for miR-200 family miRNAs (i.e., miR-141/200c and miR-200a/200b/429). We discuss in silico analysis of genes targeted by miR-200 family miRNAs and the molecular mechanisms underlying BC and RCC.
Insights
MicroRNAs (miRNAs) play a role in bladder cancer (BC) and renal cell carcinoma (RCC). This review highlights differing miRNA expression patterns in BC versus RCC, focusing on the miR-200 family.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Bladder cancer (BC) and renal cell carcinoma (RCC) are common urinary tract malignancies.
- While molecular-targeted therapies have advanced RCC treatment, BC lacks approved targeted therapeutics.
- MicroRNAs (miRNAs), small noncoding RNAs regulating gene expression, are implicated in cancer pathogenesis.
Purpose of the Study:
- To review recent miRNA expression signatures in BC and RCC.
- To identify consistently dysregulated miRNAs across multiple studies for both cancers.
- To explore the contrasting expression patterns of the miR-200 family in BC and RCC.
Main Methods:
- Systematic review of published miRNA expression signatures for BC and RCC.
- Focus on miRNAs showing consistent downregulation or upregulation across studies.
- In silico analysis to predict target genes of key miRNAs, particularly the miR-200 family.
Main Results:
- Identification of specific miRNA expression signatures associated with BC and RCC.
- Discovery of opposite expression trends for the miR-200 family miRNAs (miR-141/200c, miR-200a/200b/429) between BC and RCC.
- In silico analysis provides insights into potential target genes regulated by the miR-200 family in these cancers.
Conclusions:
- Aberrantly expressed miRNAs are crucial in the pathogenesis of BC and RCC.
- The opposing expression of miR-200 family miRNAs in BC versus RCC suggests distinct roles and potential therapeutic avenues.
- Further investigation into miR-200 family targets and mechanisms is warranted for understanding and treating these cancers.
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