Identification of succinylation-related genes in bladder cancer: integration of single-cell and transcriptomic data - Scorecard - MDSpire

Identification of succinylation-related genes in bladder cancer: integration of single-cell and transcriptomic data

  • By

  • Jiajian Yang

  • Zhengyao You

  • Haojie Mo

  • Jinxian Pu

  • Gang Shen

  • Zhijun Miao

  • May 15, 2026

  • 0 min

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Clinical Scorecard: Discovery of Genes Associated with Succinylation in Bladder Cancer: A Combined Analysis of Single-Cell and Transcriptomic Data

At a Glance

CategoryDetail
ConditionBladder Cancer (BLCA)
Key MechanismsSuccinylation-related genes (SRGs) linked to tumor progression and immune evasion.
Target PopulationPatients with bladder cancer, particularly those with non-muscle-invasive and muscle-invasive subtypes.
Care SettingOncology clinics and research settings focusing on bladder cancer.

Key Highlights

  • Identification of KCTD16, CD3D, and GSDMB as prognostic genes.
  • Development of a risk model with predictive accuracy (AUC > 0.7).
  • High-risk group shows enhanced immune evasion and altered tumor microenvironment.
  • Single-cell analysis reveals key epithelial cell subpopulations.
  • Functional assays confirm tumor-suppressive roles of GSDMB and KCTD16.

Guideline-Based Recommendations

Diagnosis

  • Utilize transcriptomic sequencing for identifying prognostic SRGs.

Management

  • Incorporate SRGs into risk models for personalized therapy.

Monitoring & Follow-up

  • Assess expression profiles of identified SRGs for prognostic evaluation.

Risks

  • Consider high recurrence and progression rates in NMIBC and low survival rates in MIBC.

Patient & Prescribing Data

Bladder cancer patients, especially those with varying stages of disease.

Targeting succinylation-related pathways may enhance therapeutic outcomes.

Clinical Best Practices

  • Integrate single-cell RNA sequencing with transcriptomic data for comprehensive analysis.
  • Focus on immune profiling to understand tumor microenvironment dynamics.
  • Validate prognostic genes through functional assays.

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