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Purpose <p>Xanthine dehydrogenase (XDH) serves as a key enzyme in purine metabolism and plays a significant role in carcinogenesis. However, the clinical significance of XDH in urothelial carcinoma (UC) progression remains unclear. Using a transcriptomic UC database (GSE32894), we found that among the genes related to XDH activity (GO:0004854), XDH was significantly downregulated during UC progression. Therefore, we aimed to assess the prognostic value of XDH immunoexpression in urinary bladder UC (UBUC) and upper tract UC (UTUC) patients.</p> Methods <p>Immunohistochemical staining for XDH was performed on 340 UTUC and 295 UBUC specimens. The association of XDH expression with clinicopathological features and patients’ outcomes, including disease-specific survival (DSS) and metastasis-free survival (MFS), was analyzed using Pearson’s chi-square test, Kaplan–Meier analysis, and multivariate Cox proportional hazards model to identify independent prognosticators.</p> Results <p>Low XDH expression was significantly associated with high tumor stage, nodal metastasis, high tumor grade, perineural invasion, vascular invasion, and a high mitotic rate (all <i>P</i> &lt; 0.01). Kaplan–Meier survival curves showed that low XDH expression was associated with poor DSS and MFS (both <i>p</i> &lt; 0.001). After adjusting for the standard pathological parameters, XDH expression status was an independent prognostic factor for DSS and MFS in UBUC and UTUC (all <i>P</i> &lt; 0.01) in the multivariate analysis model. To associate XDH with potential functions in UC, gene co-expression examination was performed using the GO classification system. XDH upregulation was linked to pyroptosis and desmosomes.</p> Conclusion <p>Low XDH expression correlates with aggressive pathological features and poor oncological outcomes, indicating its prognostic and therapeutic significances in patients with UC.</p>

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Exploring XDH expression as a prognostic marker for urothelial carcinoma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月26日

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  • Meng-Yun Hung,
  • Chien-Feng Li,
  • Hsiang-Ying Lee,
  • Hung-Lung Ke,
  • Yow-Ling Shiue,
  • Hsin-Chih Yeh,
  • Wen-Jeng Wu,
  • Yu-Ching Wei,
  • Wei-Ming Li

摘要

Purpose

Xanthine dehydrogenase (XDH) serves as a key enzyme in purine metabolism and plays a significant role in carcinogenesis. However, the clinical significance of XDH in urothelial carcinoma (UC) progression remains unclear. Using a transcriptomic UC database (GSE32894), we found that among the genes related to XDH activity (GO:0004854), XDH was significantly downregulated during UC progression. Therefore, we aimed to assess the prognostic value of XDH immunoexpression in urinary bladder UC (UBUC) and upper tract UC (UTUC) patients.

Methods

Immunohistochemical staining for XDH was performed on 340 UTUC and 295 UBUC specimens. The association of XDH expression with clinicopathological features and patients’ outcomes, including disease-specific survival (DSS) and metastasis-free survival (MFS), was analyzed using Pearson’s chi-square test, Kaplan–Meier analysis, and multivariate Cox proportional hazards model to identify independent prognosticators.

Results

Low XDH expression was significantly associated with high tumor stage, nodal metastasis, high tumor grade, perineural invasion, vascular invasion, and a high mitotic rate (all P < 0.01). Kaplan–Meier survival curves showed that low XDH expression was associated with poor DSS and MFS (both p < 0.001). After adjusting for the standard pathological parameters, XDH expression status was an independent prognostic factor for DSS and MFS in UBUC and UTUC (all P < 0.01) in the multivariate analysis model. To associate XDH with potential functions in UC, gene co-expression examination was performed using the GO classification system. XDH upregulation was linked to pyroptosis and desmosomes.

Conclusion

Low XDH expression correlates with aggressive pathological features and poor oncological outcomes, indicating its prognostic and therapeutic significances in patients with UC.