A retrospective analysis of ezrin protein and mRNA expression in breast cancer: Ezrin expression is associated with patient survival and survival of patients with receptor‐positive disease
Introduction The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less tha...
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Published in | Cancer medicine (Malden, MA) Vol. 12; no. 9; pp. 10908 - 10916 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
John Wiley & Sons, Inc
01.05.2023
John Wiley and Sons Inc Wiley |
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Abstract | Introduction
The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early‐stage breast cancer patients using the Nottingham (n = 1094) and METABRIC (n = 1980) cohorts, respectively.
Results
High expression of ezrin was significantly associated with larger tumour size (p = 0.027), higher tumour grade (p < 0.001), worse Nottingham Prognostic Index prognostic group (p = 0.011) and HER2‐positive status (p = 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (p < 0.001) and remained associated with survival in multivariate Cox‐regression analysis (p = 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051–1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (p < 0.001) in comparison to those categorised as triple‐negative breast cancer (p = 0.889). High expression of ezrin mRNA (VIL2) in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (p < 0.001).
Conclusion
Retrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor‐positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early‐stage breast cancer.
Ezrin expression is associated with clinical outcome of breast cancer patients. |
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AbstractList | Abstract
Introduction
The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early‐stage breast cancer patients using the Nottingham (
n
= 1094) and METABRIC (
n
= 1980) cohorts, respectively.
Results
High expression of ezrin was significantly associated with larger tumour size (
p
= 0.027), higher tumour grade (
p
< 0.001), worse Nottingham Prognostic Index prognostic group (
p
= 0.011) and HER2‐positive status (
p
= 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (
p
< 0.001) and remained associated with survival in multivariate Cox‐regression analysis (
p
= 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051–1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (
p
< 0.001) in comparison to those categorised as triple‐negative breast cancer (
p
= 0.889). High expression of ezrin mRNA (
VIL2)
in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (
p
< 0.001).
Conclusion
Retrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor‐positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early‐stage breast cancer. The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early-stage breast cancer patients using the Nottingham (n = 1094) and METABRIC (n = 1980) cohorts, respectively. High expression of ezrin was significantly associated with larger tumour size (p = 0.027), higher tumour grade (p < 0.001), worse Nottingham Prognostic Index prognostic group (p = 0.011) and HER2-positive status (p = 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (p < 0.001) and remained associated with survival in multivariate Cox-regression analysis (p = 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051-1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (p < 0.001) in comparison to those categorised as triple-negative breast cancer (p = 0.889). High expression of ezrin mRNA (VIL2) in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (p < 0.001). Retrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor-positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early-stage breast cancer. Introduction The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early‐stage breast cancer patients using the Nottingham (n = 1094) and METABRIC (n = 1980) cohorts, respectively. Results High expression of ezrin was significantly associated with larger tumour size (p = 0.027), higher tumour grade (p < 0.001), worse Nottingham Prognostic Index prognostic group (p = 0.011) and HER2‐positive status (p = 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (p < 0.001) and remained associated with survival in multivariate Cox‐regression analysis (p = 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051–1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (p < 0.001) in comparison to those categorised as triple‐negative breast cancer (p = 0.889). High expression of ezrin mRNA (VIL2) in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (p < 0.001). Conclusion Retrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor‐positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early‐stage breast cancer. Ezrin expression is associated with clinical outcome of breast cancer patients. Ezrin expression is associated with clinical outcome of breast cancer patients. INTRODUCTIONThe cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early-stage breast cancer patients using the Nottingham (n = 1094) and METABRIC (n = 1980) cohorts, respectively. RESULTSHigh expression of ezrin was significantly associated with larger tumour size (p = 0.027), higher tumour grade (p < 0.001), worse Nottingham Prognostic Index prognostic group (p = 0.011) and HER2-positive status (p = 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (p < 0.001) and remained associated with survival in multivariate Cox-regression analysis (p = 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051-1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (p < 0.001) in comparison to those categorised as triple-negative breast cancer (p = 0.889). High expression of ezrin mRNA (VIL2) in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (p < 0.001). CONCLUSIONRetrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor-positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early-stage breast cancer. Abstract Introduction The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic value of ezrin has been previously evaluated in breast cancer, most studies to date have been conducted in smaller cohorts (less than 500 cases) or have focused on specific disease characteristics. The current study is the largest of its kind to evaluate ezrin both at the protein and mRNA levels in early‐stage breast cancer patients using the Nottingham (n = 1094) and METABRIC (n = 1980) cohorts, respectively. Results High expression of ezrin was significantly associated with larger tumour size (p = 0.027), higher tumour grade (p < 0.001), worse Nottingham Prognostic Index prognostic group (p = 0.011) and HER2‐positive status (p = 0.001). High ezrin expression was significantly associated with adverse survival of breast cancer patients (p < 0.001) and remained associated with survival in multivariate Cox‐regression analysis (p = 0.018, hazard ratio (HR) = 1.343, 95% confidence interval (CI) = 1.051–1.716) when potentially confounding factors were included. High ezrin expression was significantly associated with adverse survival of patients whose tumours were categorised as receptor (oestrogen receptor (ER), progesterone receptor (PgR) or HER2) positive (p < 0.001) in comparison to those categorised as triple‐negative breast cancer (p = 0.889). High expression of ezrin mRNA (VIL2) in the METABRIC cohort was also significantly associated with adverse survival of breast cancer patients (p < 0.001). Conclusion Retrospective analyses show that ezrin is an independent prognostic marker, with higher expression associated with shortened survival in receptor‐positive (ER, PgR or HER2) patients. Ezrin expression is associated with more aggressive disease and may have clinical utility as a biomarker of patient prognosis in early‐stage breast cancer. |
Author | Hoskin, Victoria Martin, Stewart G. Green, Andrew Greer, Peter A. Storr, Sarah J. Ghaffari, Abdi Rakha, Emad Aiyappa‐Maudsley, Radhika Ellis, Ian O. Varma, Sonal |
AuthorAffiliation | 2 Division of Cancer Biology and Genetics, Queen's Cancer Research Institute Queen's University Kingston Ontario Canada 1 Nottingham Breast Cancer Research Centre, Biodiscovery Institute University of Nottingham, School of Medicine Nottingham UK 3 Department of Pathology and Molecular Medicine Queen's University Kingston Ontario Canada |
AuthorAffiliation_xml | – name: 1 Nottingham Breast Cancer Research Centre, Biodiscovery Institute University of Nottingham, School of Medicine Nottingham UK – name: 2 Division of Cancer Biology and Genetics, Queen's Cancer Research Institute Queen's University Kingston Ontario Canada – name: 3 Department of Pathology and Molecular Medicine Queen's University Kingston Ontario Canada |
Author_xml | – sequence: 1 givenname: Sarah J. surname: Storr fullname: Storr, Sarah J. organization: University of Nottingham, School of Medicine – sequence: 2 givenname: Victoria surname: Hoskin fullname: Hoskin, Victoria organization: Queen's University – sequence: 3 givenname: Radhika surname: Aiyappa‐Maudsley fullname: Aiyappa‐Maudsley, Radhika organization: University of Nottingham, School of Medicine – sequence: 4 givenname: Abdi surname: Ghaffari fullname: Ghaffari, Abdi organization: Queen's University – sequence: 5 givenname: Sonal surname: Varma fullname: Varma, Sonal organization: Queen's University – sequence: 6 givenname: Andrew surname: Green fullname: Green, Andrew organization: University of Nottingham, School of Medicine – sequence: 7 givenname: Emad surname: Rakha fullname: Rakha, Emad organization: University of Nottingham, School of Medicine – sequence: 8 givenname: Ian O. surname: Ellis fullname: Ellis, Ian O. organization: University of Nottingham, School of Medicine – sequence: 9 givenname: Peter A. surname: Greer fullname: Greer, Peter A. organization: Queen's University – sequence: 10 givenname: Stewart G. orcidid: 0000-0002-2810-2338 surname: Martin fullname: Martin, Stewart G. email: stewart.martin@nottingham.ac.uk organization: University of Nottingham, School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36938826$$D View this record in MEDLINE/PubMed |
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Copyright | 2023 The Authors. published by John Wiley & Sons Ltd. 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | VIL2 breast cancer ezrin EZR |
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publication-title: Exp Ther Med contributor: fullname: Fernando H – ident: e_1_2_10_23_1 doi: 10.1385/ENDO:22:2:119 – ident: e_1_2_10_4_1 doi: 10.1242/jcs.105.4.1025 – ident: e_1_2_10_6_1 doi: 10.1186/s13058-018-1079-7 – ident: e_1_2_10_10_1 doi: 10.1007/s10585-006-9050-x – ident: e_1_2_10_15_1 doi: 10.1111/1759-7714.13174 – ident: e_1_2_10_17_1 doi: 10.1038/nature10983 – ident: e_1_2_10_18_1 doi: 10.1186/1471-2407-14-995 – ident: e_1_2_10_7_1 doi: 10.1038/srep17903 – ident: e_1_2_10_2_1 doi: 10.1038/nrm2866 – ident: e_1_2_10_3_1 doi: 10.1073/pnas.96.13.7300 – ident: e_1_2_10_12_1 doi: 10.3760/cma.j.issn.0366-6999.20110738 – ident: e_1_2_10_9_1 doi: 10.1007/s10549-005-9133-4 – ident: e_1_2_10_19_1 doi: 10.1038/s41598-019-53529-z – ident: e_1_2_10_24_1 doi: 10.1074/jbc.RA118.004143 – ident: e_1_2_10_13_1 doi: 10.1038/s41416-019-0383-z – ident: e_1_2_10_22_1 doi: 10.1371/journal.pone.0022439 – ident: e_1_2_10_8_1 doi: 10.1007/s13402-013-0153-5 – ident: e_1_2_10_14_1 doi: 10.3389/fonc.2022.831507 – ident: e_1_2_10_21_1 doi: 10.1158/1078-0432.CCR-04-0713 – ident: e_1_2_10_5_1 doi: 10.1083/jcb.97.2.425 – ident: e_1_2_10_16_1 doi: 10.1530/EC-19-0164 – ident: e_1_2_10_20_1 doi: 10.1111/jcmm.16447 |
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Snippet | Introduction
The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and... The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and prognostic... Abstract Introduction The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the... IntroductionThe cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and... INTRODUCTIONThe cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the clinical and... Ezrin expression is associated with clinical outcome of breast cancer patients. Abstract Introduction The cytoskeletal protein ezrin is upregulated in many cancer types and is strongly associated with poor patient outcome. While the... |
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SubjectTerms | Antibodies Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Breast cancer Breast Neoplasms - pathology Cancer therapies Chemotherapy Clinical outcomes Cytoskeletal Proteins - genetics Cytoskeletal Proteins - metabolism Cytoskeleton ErbB-2 protein Estrogen receptors EZR Ezrin Female Gene expression Humans Lymphatic system Mastectomy Patients Progesterone Prognosis Protein expression Proteins Receptor, ErbB-2 - genetics Receptor, ErbB-2 - metabolism Receptors, Progesterone Research ethics Retrospective Studies Survival Survival analysis Tumors Values Variables VIL2 |
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Title | A retrospective analysis of ezrin protein and mRNA expression in breast cancer: Ezrin expression is associated with patient survival and survival of patients with receptor‐positive disease |
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