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Updated: Jun 9, 2025

Culture of Bladder Cancer Organoids as Precision Medicine Tools
Published on: December 28, 2021
Molecular Landscape of Bladder Cancer: Key Genes, Transcription Factors, and Drug Interactions
Danishuddin1, Md Azizul Haque1, Shawez Khan2
1Department of Biotechnology, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Abstract:
Bladder cancer is among the most prevalent tumors in the urinary system and is known for its high malignancy. Although traditional diagnostic and treatment methods are established, recent research has focused on understanding the molecular mechanisms underlying bladder cancer. The primary objective of this study is to identify novel diagnostic markers and discover more effective targeted therapies for bladder cancer. This study identified differentially expressed genes (DEGs) between bladder cancer tissues and adjacent normal tissues using data from The Cancer Genome Atlas (TCGA). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were conducted to explore the functional roles of these genes. A protein-protein interaction (PPI) network was also constructed to identify and analyze hub genes within this network. Gene set variation analysis (GSVA) was conducted to investigate the involvement of these genes in various biological processes and pathways. Ten key genes were found to be significantly associated with bladder cancer: IL6, CCNA2, CCNB1, CDK1, PLK1, TOP2A, AURKA, AURKB, FOXM1, and CALML5. GSVA analyses revealed that these genes are involved in a variety of biological processes and signaling pathways, including coagulation, UV-response-down, apoptosis, Notch signaling, and Wnt/beta-catenin signaling. The diagnostic relevance of these genes was validated through ROC curve analysis. Additionally, potential therapeutic drug interactions with these key genes were identified. This study provides valuable insights into key genes and their roles in bladder cancer. The identified genes and their interactions with therapeutic drugs could serve as potential biomarkers, presenting new opportunities for enhancing the diagnosis and prognosis of bladder cancer.
Insights
This study identifies ten key genes involved in bladder cancer progression. These genes offer potential for developing new diagnostic markers and targeted therapies for improved patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Bladder cancer is a highly malignant urinary system tumor with established treatments.
- Recent research focuses on elucidating molecular mechanisms for novel therapeutic strategies.
- Understanding gene expression is crucial for identifying diagnostic markers and targeted therapies.
Purpose of the Study:
- To identify novel diagnostic markers for bladder cancer.
- To discover more effective targeted therapies for bladder cancer.
- To explore the molecular mechanisms underlying bladder cancer.
Main Methods:
- Utilized The Cancer Genome Atlas (TCGA) data to identify differentially expressed genes (DEGs).
- Performed Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses.
- Constructed a protein-protein interaction (PPI) network and conducted Gene Set Variation Analysis (GSVA).
Main Results:
- Identified ten key genes significantly associated with bladder cancer: IL6, CCNA2, CCNB1, CDK1, PLK1, TOP2A, AURKA, AURKB, FOXM1, and CALML5.
- GSVA revealed these genes' involvement in coagulation, UV-response-down, apoptosis, Notch, and Wnt/beta-catenin signaling pathways.
- Validated diagnostic relevance using ROC curve analysis and identified potential drug interactions.
Conclusions:
- The ten identified key genes provide valuable insights into bladder cancer pathogenesis.
- These genes and their drug interactions may serve as potential biomarkers for diagnosis and prognosis.
- This research opens new avenues for enhancing bladder cancer diagnosis and treatment strategies.
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