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Translational Advances in Urothelial Carcinoma: From Bench to Bedside.

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International journal of urology : official journal of the Japanese Urological Association 📖 저널 OA 27.2% 2021: 1/3 OA 2024: 2/2 OA 2025: 12/45 OA 2026: 15/56 OA 2021~2026 2026 Vol.33(1) p. e70341
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Iwasawa T, Tsujino T, Tsukahara S, Fukushima H, Ito D, Tomiyama E, Urabe F

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Urothelial carcinoma (UC), encompassing both bladder cancer and upper tract UC, is a biologically heterogeneous malignancy that has long complicated patient stratification and therapeutic prediction.

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APA Iwasawa T, Tsujino T, et al. (2026). Translational Advances in Urothelial Carcinoma: From Bench to Bedside.. International journal of urology : official journal of the Japanese Urological Association, 33(1), e70341. https://doi.org/10.1111/iju.70341
MLA Iwasawa T, et al.. "Translational Advances in Urothelial Carcinoma: From Bench to Bedside.." International journal of urology : official journal of the Japanese Urological Association, vol. 33, no. 1, 2026, pp. e70341.
PMID 41531330 ↗
DOI 10.1111/iju.70341

Abstract

Urothelial carcinoma (UC), encompassing both bladder cancer and upper tract UC, is a biologically heterogeneous malignancy that has long complicated patient stratification and therapeutic prediction. Recent genomic and transcriptomic analyses, however, have delineated reproducible molecular subtypes across non-muscle-invasive and muscle-invasive disease. These classification frameworks have refined biological understanding and improved both risk stratification and treatment selection. Emerging evidence also indicates that genomic alterations, such as FGFR3 mutations, may confer distinct immunologic phenotypes within specific transcriptomic contexts, thereby challenging prior assumptions. The advent of immune checkpoint inhibitors has transformed UC management, yet variable response rates underscore the complexity of the tumor microenvironment (TME). Single-cell and spatial analyses have identified immune-inflamed, -desert, and -excluded TME subtypes, with cancer-associated fibroblasts playing a key role in immune exclusion and therapeutic resistance. Liquid biopsy, particularly circulating tumor DNA, has demonstrated utility for real-time disease monitoring, minimal residual disease detection, and treatment stratification, as highlighted in trials such as IMvigor010 and IMvigor011. Urinary extracellular vesicles also represent promising non-invasive biomarkers, though further standardization is required. In addition, novel therapeutic strategies-including antibody-drug conjugates, gene therapies, and sustained-release delivery systems-are broadening treatment options across disease stages. Collectively, these translational advances mark a paradigm shift toward precision immuno-oncology in UC. Nonetheless, successful clinical implementation will require prospective validation, optimized analytical platforms, and sustained physician-scientist engagement to translate these discoveries into improved patient outcomes. This review provides a comprehensive overview of recent progress in UC translational research, with a focus on genomic and transcriptomic insights, the evolving role of immunotherapy, advances in liquid biopsy, and the development of novel therapeutics.

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