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Table · dataset · 2026

<p>Meta-analysis and revision sensitivity audit.</p>

Listed in figshare and Loughborough Research Repository — shown once because both records carry DOI 10.1371/journal.pone.0358043.t006

<div><p>Immune checkpoint inhibitors benefit only a subset of patients with urothelial carcinoma, and bulk biomarkers may not capture spatially organized stromal and vascular programs that restrict immune access.

Description

We performed a retrospective public multi-cohort transcriptomic study to examine whether a cancer-associated fibroblast (CAF)/TGF-beta/endothelial barrier direction is associated with immune exclusion and checkpoint resistance in bladder cancer.

GSE171351 was used for spatial discovery, GSE319536 for external spatial recurrence testing, TCGA-BLCA for prognosis-oriented support, and IMvigor210, GSE176307 and GSE328930/DUTRENEO for treatment-response projection. In the four-section discovery cohort, rank-5 non-negative matrix factorization separated an E2 barrier-enriched program from an E4 hypoxic epithelial program, although component assignment was strongly associated with section identity.

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The external cohort reproduced the direct CAF/TGF-beta/endothelial barrier direction in 22 of 22 sections but did not reproduce E2/E4 mutual exclusivity: projected E2 and E4 were positively correlated (rho = 0.928). In IMvigor210, top-quartile E2-high tumors showed suggestive, but not statistically conclusive, evidence of anti-PD-L1 non-response after full biologic covariate adjustment (OR=2.57, 95% CI 1.00–6.64, p = 0.051; delta AUC = 0.009).

A prespecified heuristic barrier-exclusion score was associated with non-response in exploratory fixed- and random-effects summaries (OR=1.52, 95% CI 1.20–1.92), including a sensitivity analysis excluding GSE328930. These results identify a recurrent barrier direction rather than a universal two-niche architecture and support a hypothesis-generating mechanism-to-translation framework that requires prospective spatial and pathology-level validation.</p></div>

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Provenance · 2 source records, 41 field assertions
SourceKeyLast seenRaw
figshareoai:figshare.com:article/3396698612 d agoJSON v1
Loughborough Research Repositoryoai:figshare.com:article/3396698612 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[disease].local:disease:cancermapping · figshare comvocabulary-mapper@1.0.0keywords['Cancer']
concepts[field].anzsrc:field:320211mapping · repository lboro ac ukvocabulary-mapper@1.0.0keywords['Infectious Diseases']
concepts[field].anzsrc:field:320211mapping · figshare comvocabulary-mapper@1.0.0keywords['Infectious Diseases']
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concepts[field].anzsrc:field:440710mapping · repository lboro ac ukvocabulary-mapper@1.0.0keywords['Science Policy']
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concepts[field].anzsrc:group:3105mapping · figshare comvocabulary-mapper@1.0.0keywords['Genetics']
concepts[field].anzsrc:group:3105mapping · repository lboro ac ukvocabulary-mapper@1.0.0keywords['Genetics']
concepts[field].anzsrc:group:3204mapping · figshare comvocabulary-mapper@1.0.0keywords['Immunology']
concepts[field].anzsrc:group:3204mapping · repository lboro ac ukvocabulary-mapper@1.0.0keywords['Immunology']
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