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pmid:35004669

LCK and CD3E Orchestrate the Tumor Microenvironment and Promote Immunotherapy Response and Survival of Muscle-Invasive Bladder Cancer Patients.

Xiaonan Zheng · Xinyang Liao · Ling Nie · Tianhai Lin · Hang Xu · Lu Yang · Bairong Shen · Shi Qiu · Jianzhong Ai · Qiang Wei

Frontiers in cell and developmental biology · 2021 doi:10.3389/fcell.2021.748280

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35004669
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2026-11-01T17:36:44Z
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paper object · 10 fields
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title
LCK and CD3E Orchestrate the Tumor Microenvironment and Promote Immunotherapy Response and Survival of Muscle-Invasive Bladder Cancer Patients.
doi
10.3389/fcell.2021.748280
pmid
35004669
authors array · 10 items
[0]
Xiaonan Zheng
[1]
Xinyang Liao
[2]
Ling Nie
[3]
Tianhai Lin
[4]
Hang Xu
[5]
Lu Yang
[6]
Bairong Shen
[7]
Shi Qiu
[8]
Jianzhong Ai
[9]
Qiang Wei
journal
Frontiers in cell and developmental biology
year
2021
abstract
Background: Studies have demonstrated the significance of multiple biomarkers for bladder cancer. Here, we attempt to present biomarkers potentially predictive of the prognosis and immunotherapy response of muscle-invasive bladder cancer (MIBC). Method: Immune and stromal scores were calculated for MIBC patients from The Cancer Genome Atlas (TCGA). Core differential expression genes (DEGs) with prognostic value were identified and validated using an independent dataset GSE31684. The clinical implications of prognostic genes and the inter-gene correlation were presented. The distribution of tumor-infiltrating immune cells (TICs), the correlation with tumor mutation burden (TMB), and the expression of eight immune checkpoint-relevant genes and CD39 were accordingly compared. Two bladder cancer cohorts (GSE176307 and IMvigor210) receiving immunotherapy were recruited to validate the prognostic value of LCK and CD3E for immunotherapy. Results: 361 MIBC samples from TCGA revealed a worse overall survival for higher stromal infiltration (p = 0.009) but a better overall survival for higher immune infiltration (p = 0.042). CD3E and LCK were independently validated by TCGA and GSE31684 to be prognostic for MIBC. CD3E was the most correlative gene of LCK, with a coefficient of r = 0.86 (p < 0.001). CD8+ T cells and macrophage M1 are more abundant in favor of a higher expression of CD3E and LCK in MIBC and across pan-cancers. Immune checkpoints like CTLA4, CD274 (PD-1), and PDCD1 (PD-L1) were highly expressed in high-CD3E and high-LCK groups for MIBC and also for pan-cancers, except for thymoma. LCK and CD3E had a moderate positive correlation with CD39 expression. Importantly, high-LCK and high-CD3E groups had a higher percentage of responders than the low-expression groups both in GSE176307 (LCK: 22.73vs. 13.64%, CD3E: 22.00 vs. 13.16%) and IMvigor210 cohorts (LCK: 28.19 vs. 17.45%, CD3E: 25.50 vs. 20.13%). Conclusion: CD3E and LCK were potential biomarkers of MIBC. CD3E and LCK were positively correlated with several regular immunotherapy biomarkers, which is supported by real-world outcomes from two immunotherapy cohorts.
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The prognostic value of the genes present in the core modules of the PPI network was evaluated with Kaplan–Meier curves.
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sections[4] "Identification of Prognostic Genes" paragraph 3
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The prognostic value of the genes present in the core modules of the PPI network was evaluated with Kaplan–Meier curves.
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sections[14] "Data Availability Statement" paragraph 2
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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CD3E and LCK were the prognostic genes of MIBC after external validation with GSE31684.
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sections[7] "CD3E and LCK Are the Prognostic Genes of MIBC" paragraph 5
quote
Survival curves demonstrated that CD3E (TCGA: p = 0.041, GEO: p = 0.022) and LCK (TCGA: p = 0.026, GEO: p = 0.024) were the prognostic genes of MIBC after external validation with GSE31684 (Figures 2D–G).
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CD3E and LCK were the prognostic genes of MIBC after external validation with GSE31684.
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Fibroblast Growth Factor Receptor 3 Alterations and Response to Immune Checkpoint Inhibition in Metastatic Urothelial Cancer: A Real World Experience
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title
Combination of a novel gene expression signature with a clinical nomogram improves the prediction of survival in high-risk bladder cancer  
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35004669", "kind": "science-record", "revision": 4, "content_hash": "sha256:d045ddf5d57c3ac73960bf5f0a7b13cd1259c9f8ab21a602e887a0019ed3f98d", "created_at": "2026-11-01T17:36:44Z", "updated_at": "2026-11-01T22:05:33Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "LCK and CD3E Orchestrate the Tumor Microenvironment and Promote Immunotherapy Response and Survival of Muscle-Invasive Bladder Cancer Patients.", "doi": "10.3389/fcell.2021.748280", "pmid": "35004669", "authors": ["Xiaonan Zheng", "Xinyang Liao", "Ling Nie", "Tianhai Lin", "Hang Xu", "Lu Yang", "Bairong Shen", "Shi Qiu", "Jianzhong Ai", "Qiang Wei"], "journal": "Frontiers in cell and developmental biology", "year": 2021, "abstract": "Background: Studies have demonstrated the significance of multiple biomarkers for bladder cancer. Here, we attempt to present biomarkers potentially predictive of the prognosis and immunotherapy response of muscle-invasive bladder cancer (MIBC). Method: Immune and stromal scores were calculated for MIBC patients from The Cancer Genome Atlas (TCGA). Core differential expression genes (DEGs) with prognostic value were identified and validated using an independent dataset GSE31684. The clinical implications of prognostic genes and the inter-gene correlation were presented. The distribution of tumor-infiltrating immune cells (TICs), the correlation with tumor mutation burden (TMB), and the expression of eight immune checkpoint-relevant genes and CD39 were accordingly compared. Two bladder cancer cohorts (GSE176307 and IMvigor210) receiving immunotherapy were recruited to validate the prognostic value of LCK and CD3E for immunotherapy. Results: 361 MIBC samples from TCGA revealed a worse overall survival for higher stromal infiltration (p = 0.009) but a better overall survival for higher immune infiltration (p = 0.042). CD3E and LCK were independently validated by TCGA and GSE31684 to be prognostic for MIBC. CD3E was the most correlative gene of LCK, with a coefficient of r = 0.86 (p < 0.001). CD8+ T cells and macrophage M1 are more abundant in favor of a higher expression of CD3E and LCK in MIBC and across pan-cancers. Immune checkpoints like CTLA4, CD274 (PD-1), and PDCD1 (PD-L1) were highly expressed in high-CD3E and high-LCK groups for MIBC and also for pan-cancers, except for thymoma. LCK and CD3E had a moderate positive correlation with CD39 expression. Importantly, high-LCK and high-CD3E groups had a higher percentage of responders than the low-expression groups both in GSE176307 (LCK: 22.73vs. 13.64%, CD3E: 22.00 vs. 13.16%) and IMvigor210 cohorts (LCK: 28.19 vs. 17.45%, CD3E: 25.50 vs. 20.13%). Conclusion: CD3E and LCK were potential biomarkers of MIBC. CD3E and LCK were positively correlated with several regular immunotherapy biomarkers, which is supported by real-world outcomes from two immunotherapy cohorts.", "claims": [{"id": "claim-method", "statement": "The prognostic value of the genes present in the core modules of the PPI network was evaluated with Kaplan–Meier curves.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35004669", "locator": "sections[4] \"Identification of Prognostic Genes\" paragraph 3", "quote": "The prognostic value of the genes present in the core modules of the PPI network was evaluated with Kaplan–Meier curves."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35004669", "locator": "sections[14] \"Data Availability Statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "CD3E and LCK were the prognostic genes of MIBC after external validation with GSE31684.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35004669", "locator": "sections[7] \"CD3E and LCK Are the Prognostic Genes of MIBC\" paragraph 5", "quote": "Survival curves demonstrated that CD3E (TCGA: p = 0.041, GEO: p = 0.022) and LCK (TCGA: p = 0.026, GEO: p = 0.024) were the prognostic genes of MIBC after external validation with GSE31684 (Figures 2D–G)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "CD3E and LCK were the prognostic genes of MIBC after external validation with GSE31684.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:35004669"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE176307"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE176307"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35004669", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fcell.2021.748280", "sha256": "sha256:c9c886eb58e83978aebdbec3d027fd2733ef069c779c403799552b412932eb36", "bytes": 27422, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fcell.2021.748280", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC8740181", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE176307", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE176307", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE176307", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE31684", "GSE176307"], "resolved_accessions": ["GSE31684", "GSE176307"], "statements": ["The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material."], "basis": "The paper names GSE31684, GSE176307 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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