Osteopontin is a prognostic biomarker in non-small cell lung cancer

Abstract Background In a previously published report we characterized the expression of the metastasis-associated proteins S100A4, osteopontin (OPN) and ephrin-A1 in a prospectively collected panel of non-small cell lung cancer (NSCLC) tumors. The aim of the present follow-up study was to investigat...

Full description

Saved in:
Bibliographic Details
Main Authors: Ane Kongsgaard, Kjetil Boye, Miriam Øijordsbakken, Marius Lund-Iversen, Ann Rita Halvorsen, Steinar K Solberg, Gisle Berge, Åslaug Helland, Odd Terje Brustugun, Gunhild M Mælandsmo
Format: Article
Language:English
Published: BMC 2013-11-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/1471-2407-13-540
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850109989468766208
author Ane Kongsgaard
Kjetil Boye
Miriam Øijordsbakken
Marius Lund-Iversen
Ann Rita Halvorsen
Steinar K Solberg
Gisle Berge
Åslaug Helland
Odd Terje Brustugun
Gunhild M Mælandsmo
author_facet Ane Kongsgaard
Kjetil Boye
Miriam Øijordsbakken
Marius Lund-Iversen
Ann Rita Halvorsen
Steinar K Solberg
Gisle Berge
Åslaug Helland
Odd Terje Brustugun
Gunhild M Mælandsmo
author_sort Ane Kongsgaard
collection DOAJ
description Abstract Background In a previously published report we characterized the expression of the metastasis-associated proteins S100A4, osteopontin (OPN) and ephrin-A1 in a prospectively collected panel of non-small cell lung cancer (NSCLC) tumors. The aim of the present follow-up study was to investigate the prognostic impact of these potential biomarkers in the same patient cohort. In addition, circulating serum levels of OPN were measured and single nucleotide polymorphisms (SNP) in the -443 position of the OPN promoter were analyzed. Methods Associations between immunohistochemical expression of S100A4, OPN and ephrin-A1 and relapse free and overall survival were examined using univariate and multivariate analyses. Serum OPN was measured by ELISA, polymorphisms in the -443 position of the tumor OPN promoter were analyzed by PCR, and associations between OPN levels and promoter polymorphisms and clinicopathological parameters and patient outcome were investigated. Results High expression of OPN in NSCLC tumors was associated with poor patient outcome, and OPN was a strong, independent prognostic factor for both relapse free and overall survival. Serum OPN levels increased according to tumor pT classification and tumor size, and patients with OPN-expressing tumors had higher serum levels than patients with OPN-negative tumors. S100A4 was a negative prognostic factor in several subgroups of adenocarcinoma patients, but not in the overall patient cohort. There was no association between ephrin-A1 expression and patient outcome. Conclusions OPN is a promising prognostic biomarker in NSCLC, and should be further explored in the selection of patients for adjuvant treatment following surgical resection.
format Article
id doaj-art-25115c85ff54446898a8cc99f6ed02c0
institution OA Journals
issn 1471-2407
language English
publishDate 2013-11-01
publisher BMC
record_format Article
series BMC Cancer
spelling doaj-art-25115c85ff54446898a8cc99f6ed02c02025-08-20T02:37:57ZengBMCBMC Cancer1471-24072013-11-0113111010.1186/1471-2407-13-540Osteopontin is a prognostic biomarker in non-small cell lung cancerAne Kongsgaard0Kjetil Boye1Miriam Øijordsbakken2Marius Lund-Iversen3Ann Rita Halvorsen4Steinar K Solberg5Gisle Berge6Åslaug Helland7Odd Terje Brustugun8Gunhild M Mælandsmo9Department of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Medical Biochemistry, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Pathology, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Genetics, Institute for Cancer Research, The Norwegian Radium, Hospital, Oslo University HospitalDepartment of Cardiovascular and Thoracic Surgery, Rikshospitalet, Oslo University HospitalDepartment of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Oncology, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Oncology, The Norwegian Radium Hospital, Oslo University HospitalDepartment of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo University HospitalAbstract Background In a previously published report we characterized the expression of the metastasis-associated proteins S100A4, osteopontin (OPN) and ephrin-A1 in a prospectively collected panel of non-small cell lung cancer (NSCLC) tumors. The aim of the present follow-up study was to investigate the prognostic impact of these potential biomarkers in the same patient cohort. In addition, circulating serum levels of OPN were measured and single nucleotide polymorphisms (SNP) in the -443 position of the OPN promoter were analyzed. Methods Associations between immunohistochemical expression of S100A4, OPN and ephrin-A1 and relapse free and overall survival were examined using univariate and multivariate analyses. Serum OPN was measured by ELISA, polymorphisms in the -443 position of the tumor OPN promoter were analyzed by PCR, and associations between OPN levels and promoter polymorphisms and clinicopathological parameters and patient outcome were investigated. Results High expression of OPN in NSCLC tumors was associated with poor patient outcome, and OPN was a strong, independent prognostic factor for both relapse free and overall survival. Serum OPN levels increased according to tumor pT classification and tumor size, and patients with OPN-expressing tumors had higher serum levels than patients with OPN-negative tumors. S100A4 was a negative prognostic factor in several subgroups of adenocarcinoma patients, but not in the overall patient cohort. There was no association between ephrin-A1 expression and patient outcome. Conclusions OPN is a promising prognostic biomarker in NSCLC, and should be further explored in the selection of patients for adjuvant treatment following surgical resection.https://doi.org/10.1186/1471-2407-13-540NSCLCPrognosisBiomarkerOsteopontinS100A4
spellingShingle Ane Kongsgaard
Kjetil Boye
Miriam Øijordsbakken
Marius Lund-Iversen
Ann Rita Halvorsen
Steinar K Solberg
Gisle Berge
Åslaug Helland
Odd Terje Brustugun
Gunhild M Mælandsmo
Osteopontin is a prognostic biomarker in non-small cell lung cancer
BMC Cancer
NSCLC
Prognosis
Biomarker
Osteopontin
S100A4
title Osteopontin is a prognostic biomarker in non-small cell lung cancer
title_full Osteopontin is a prognostic biomarker in non-small cell lung cancer
title_fullStr Osteopontin is a prognostic biomarker in non-small cell lung cancer
title_full_unstemmed Osteopontin is a prognostic biomarker in non-small cell lung cancer
title_short Osteopontin is a prognostic biomarker in non-small cell lung cancer
title_sort osteopontin is a prognostic biomarker in non small cell lung cancer
topic NSCLC
Prognosis
Biomarker
Osteopontin
S100A4
url https://doi.org/10.1186/1471-2407-13-540
work_keys_str_mv AT anekongsgaard osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT kjetilboye osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT miriamøijordsbakken osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT mariuslundiversen osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT annritahalvorsen osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT steinarksolberg osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT gisleberge osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT aslaughelland osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT oddterjebrustugun osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer
AT gunhildmmælandsmo osteopontinisaprognosticbiomarkerinnonsmallcelllungcancer