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Updated: Feb 2, 2026

Culture of Bladder Cancer Organoids as Precision Medicine Tools
Published on: December 28, 2021
Loss of DUSP2 predicts a poor prognosis in patients with bladder cancer
Hubin Yin1, Weiyang He2, Yunhai Li3
1Department of Urology, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China; Chongqing Key Laboratory of Molecular Oncology and Epigenetics, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Abstract:
Dual-specificity phosphatase 2 (DUSP2), a member of nuclear type I DUSP family, abolishes the activation of mitogen-activated protein kinases (MAPKs) and plays critical roles in the immune processes, inflammatory responses, and cancer progression. Currently, whether DUSP2 is involved in pathogenesis of bladder cancer remains unclear. In this study, we demonstrate that the expression level of DUSP2 was predominantly downregulated in bladder cancer tissues and cell lines as compared with that of paired normal tissues and benign urothelial cells. Besides, the expression of DUSP2 was significantly associated with pathological grade (P = .009), AJCC stage (P = .017), and subtype (P = .001) in The Cancer Genome Atlas cohort and mainly related to TNM stage (P = .016) in the tissue microarray cohort. Kaplan-Meier analysis suggested that patients with low DUSP2 expression had a shorter 5-year overall survival (P = .018 in The Cancer Genome Atlas; P = .012 in tissue microarray) and lower recurrence-free survival (P = .008). Cox regression analysis indicated that reduced DUSP2 was an independent high risk factor for survival prognosis in both cohorts. Taken together, our findings for the first time suggested DUSP2 as a progression and prognosis biomarker for bladder cancer. Whether DUSP2 functions as a tumor suppressor in bladder cancer deserves further studies.
Insights
Dual-specificity phosphatase 2 (DUSP2) is downregulated in bladder cancer, correlating with advanced stages and poor survival. Reduced DUSP2 expression indicates a worse prognosis for bladder cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Dual-specificity phosphatase 2 (DUSP2) regulates mitogen-activated protein kinases (MAPKs).
- DUSP2's role in bladder cancer pathogenesis is currently unknown.
- DUSP2 is implicated in immune processes, inflammation, and cancer progression.
Purpose of the Study:
- To investigate the expression and prognostic significance of DUSP2 in bladder cancer.
- To determine if DUSP2 is associated with bladder cancer progression and patient survival.
Main Methods:
- Analysis of DUSP2 expression in bladder cancer tissues and cell lines.
- Correlation of DUSP2 levels with clinicopathological features (grade, stage, subtype) in The Cancer Genome Atlas and tissue microarray cohorts.
- Kaplan-Meier and Cox regression analyses to assess the impact of DUSP2 on overall and recurrence-free survival.
Main Results:
- DUSP2 expression was significantly downregulated in bladder cancer tissues and cell lines compared to normal controls.
- Lower DUSP2 expression correlated with higher pathological grade, advanced AJCC/TNM stage, and specific subtypes.
- Reduced DUSP2 levels were associated with shorter overall survival and recurrence-free survival in both patient cohorts.
Conclusions:
- DUSP2 is downregulated in bladder cancer and serves as a potential biomarker for disease progression.
- Reduced DUSP2 expression is an independent predictor of poor survival prognosis in bladder cancer patients.
- Further research is warranted to elucidate DUSP2's tumor-suppressive function in bladder cancer.
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