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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Main Authors: Armand Bankhead, III, Thomas McMaster, Yin Wang, Philip S. Boonstra, Phillip L. Palmbos
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:EBioMedicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396419307716
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spelling 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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