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Patient-derived Orthotopic Xenograft Models for Human Urothelial Cell Carcinoma and Colorectal Cancer Tumor Growth and Spontaneous Metastasis
Published on: May 12, 2019
Functional Genomics Profiling of Bladder Urothelial Carcinoma MicroRNAome as a Potential Biomarker
Wei Tse Li1, Hao Zheng1, Vincent Nguyen1
1Department of Surgery, University of California, San Diego, La Jolla, California, USA.
Abstract:
Though bladder urothelial carcinoma is the most common form of bladder cancer, advances in its diagnosis and treatment have been modest in the past few decades. To evaluate miRNAs as putative disease markers for bladder urothelial carcinoma, this study develops a process to identify dysregulated miRNAs in cancer patients and potentially stratify patients based on the association of their microRNAome phenotype to genomic alterations. Using RNA sequencing data for 409 patients from the Cancer Genome Atlas, we examined miRNA differential expression between cancer and normal tissues and associated differentially expressed miRNAs with patient survival and clinical variables. We then correlated miRNA expressions with genomic alterations using the Wilcoxon test and REVEALER. We found a panel of six miRNAs dysregulated in bladder cancer and exhibited correlations to patient survival. We also performed differential expression analysis and clinical variable correlations to identify miRNAs associated with tobacco smoking, the most important risk factor for bladder cancer. Two miRNAs, miR-323a and miR-431, were differentially expressed in smoking patients compared to nonsmoking patients and were associated with primary tumor size. Functional studies of these miRNAs and the genomic features we identified for potential stratification may reveal underlying mechanisms of bladder cancer carcinogenesis and further diagnosis and treatment methods for urothelial bladder carcinoma.
Insights
This study identified six microRNAs (miRNAs) dysregulated in bladder cancer, correlating with patient survival. Two specific miRNAs, miR-323a and miR-431, are linked to smoking status and tumor size in bladder cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Bladder urothelial carcinoma, the most common bladder cancer, has seen limited diagnostic and therapeutic advances.
- MicroRNAs (miRNAs) are potential biomarkers for cancer detection and stratification.
Purpose of the Study:
- To identify dysregulated miRNAs in bladder cancer.
- To correlate miRNA expression with patient survival and clinical variables.
- To associate miRNA profiles with genomic alterations and smoking status.
Main Methods:
- Utilized RNA sequencing data from 409 Cancer Genome Atlas patients.
- Performed differential expression analysis for miRNAs between tumor and normal tissues.
- Correlated miRNA expression with survival, clinical data, and genomic alterations using Wilcoxon test and REVEALER.
Main Results:
- Identified a panel of six miRNAs significantly dysregulated in bladder cancer, associated with patient survival.
- Found two miRNAs (miR-323a and miR-431) differentially expressed in smoking patients, linked to primary tumor size.
- Established correlations between miRNA expression, genomic alterations, and clinical factors.
Conclusions:
- Dysregulated miRNAs represent potential biomarkers for bladder cancer diagnosis and patient stratification.
- Specific miRNAs are associated with smoking, a major risk factor, and tumor characteristics.
- Further functional studies on identified miRNAs and genomic features may elucidate bladder cancer mechanisms and improve treatment.
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