TP63 isoform expression is linked with distinct clinical outcomes in cancer
Background: Half of muscle-invasive bladder cancer patients will relapse with metastatic disease and molecular tests to predict relapse are needed. TP63 has been proposed as a prognostic biomarker in bladder cancer, but reports associating it with clinical outcomes are conflicting. Since TP63 is exp...
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doaj-c8425c70d14b410ab9193715ae8a848e2020-11-24T23:07:41ZengElsevierEBioMedicine2352-39642020-01-0151TP63 isoform expression is linked with distinct clinical outcomes in cancerArmand Bankhead, III0Thomas McMaster1Yin Wang2Philip S. Boonstra3Phillip L. Palmbos4Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA; Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, MI 48109, USADepartment of Internal Medicine, Hematology/Oncology Division, University of Michigan Medical School, Ann Arbor, MI 48109, USADepartment of Internal Medicine, Hematology/Oncology Division, University of Michigan Medical School, Ann Arbor, MI 48109, USADepartment of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USADepartment of Internal Medicine, Hematology/Oncology Division, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Corresponding author.Background: Half of muscle-invasive bladder cancer patients will relapse with metastatic disease and molecular tests to predict relapse are needed. TP63 has been proposed as a prognostic biomarker in bladder cancer, but reports associating it with clinical outcomes are conflicting. Since TP63 is expressed as multiple isoforms, we hypothesized that these conflicting associations with clinical outcome may be explained by distinct opposing effects of differential TP63 isoform expression. Methods: Using RNA-Seq data from The Cancer Genome Atlas (TCGA), TP63 isoform-level expression was quantified and associated with clinical covariates (e.g. survival, stage) across 8,519 patients from 29 diseases. A comprehensive catalog of TP63 isoforms was assembled using gene annotation databases and de novo discovery in bladder cancer patients. Quantifications and un-annotated TP63 isoforms were validated using quantitative RT-PCR and a separate bladder cancer cohort. Findings: DNp63 isoform expression was associated with improved bladder cancer patient survival in patients with a luminal subtype (HR = 0.89, CI 0.80–0.99, Cox p = 0.034). Conversely, TAp63 isoform expression was associated with reduced bladder cancer patient survival in patients with a basal subtype (HR = 2.35, CI 1.64–3.37, Cox p < 0.0001). These associations were observed in multiple TCGA disease cohorts and correlated with epidermal differentiation (DNp63) and immune-related (TAp63) gene signatures. Interpretation: These results comprehensively define TP63 isoform expression in human cancer and suggest that TP63 isoforms are involved in distinct transcriptional programs with opposing effects on clinical outcome. Keywords: TP63, Isoforms, Cancer, Bladder Cancer, Biomarkerhttp://www.sciencedirect.com/science/article/pii/S2352396419307716 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Armand Bankhead, III Thomas McMaster Yin Wang Philip S. Boonstra Phillip L. Palmbos |
spellingShingle |
Armand Bankhead, III Thomas McMaster Yin Wang Philip S. Boonstra Phillip L. Palmbos TP63 isoform expression is linked with distinct clinical outcomes in cancer EBioMedicine |
author_facet |
Armand Bankhead, III Thomas McMaster Yin Wang Philip S. Boonstra Phillip L. Palmbos |
author_sort |
Armand Bankhead, III |
title |
TP63 isoform expression is linked with distinct clinical outcomes in cancer |
title_short |
TP63 isoform expression is linked with distinct clinical outcomes in cancer |
title_full |
TP63 isoform expression is linked with distinct clinical outcomes in cancer |
title_fullStr |
TP63 isoform expression is linked with distinct clinical outcomes in cancer |
title_full_unstemmed |
TP63 isoform expression is linked with distinct clinical outcomes in cancer |
title_sort |
tp63 isoform expression is linked with distinct clinical outcomes in cancer |
publisher |
Elsevier |
series |
EBioMedicine |
issn |
2352-3964 |
publishDate |
2020-01-01 |
description |
Background: Half of muscle-invasive bladder cancer patients will relapse with metastatic disease and molecular tests to predict relapse are needed. TP63 has been proposed as a prognostic biomarker in bladder cancer, but reports associating it with clinical outcomes are conflicting. Since TP63 is expressed as multiple isoforms, we hypothesized that these conflicting associations with clinical outcome may be explained by distinct opposing effects of differential TP63 isoform expression. Methods: Using RNA-Seq data from The Cancer Genome Atlas (TCGA), TP63 isoform-level expression was quantified and associated with clinical covariates (e.g. survival, stage) across 8,519 patients from 29 diseases. A comprehensive catalog of TP63 isoforms was assembled using gene annotation databases and de novo discovery in bladder cancer patients. Quantifications and un-annotated TP63 isoforms were validated using quantitative RT-PCR and a separate bladder cancer cohort. Findings: DNp63 isoform expression was associated with improved bladder cancer patient survival in patients with a luminal subtype (HR = 0.89, CI 0.80–0.99, Cox p = 0.034). Conversely, TAp63 isoform expression was associated with reduced bladder cancer patient survival in patients with a basal subtype (HR = 2.35, CI 1.64–3.37, Cox p < 0.0001). These associations were observed in multiple TCGA disease cohorts and correlated with epidermal differentiation (DNp63) and immune-related (TAp63) gene signatures. Interpretation: These results comprehensively define TP63 isoform expression in human cancer and suggest that TP63 isoforms are involved in distinct transcriptional programs with opposing effects on clinical outcome. Keywords: TP63, Isoforms, Cancer, Bladder Cancer, Biomarker |
url |
http://www.sciencedirect.com/science/article/pii/S2352396419307716 |
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