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Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients

BACKGROUND: It is well known that osteopontin (OPN) plays an important role in tumor progression and that a high OPN expression level in several tumor entities correlates with poor prognosis in cancer patients. However, little is known about the prognostic relevance of the OPN mRNA splice variants....

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Autores principales: Hahnel, Antje, Wichmann, Henri, Greither, Thomas, Kappler, Matthias, Würl, Peter, Kotzsch, Matthias, Taubert, Helge, Vordermark, Dirk, Bache, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364873/
https://www.ncbi.nlm.nih.gov/pubmed/22471890
http://dx.doi.org/10.1186/1471-2407-12-131
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author Hahnel, Antje
Wichmann, Henri
Greither, Thomas
Kappler, Matthias
Würl, Peter
Kotzsch, Matthias
Taubert, Helge
Vordermark, Dirk
Bache, Matthias
author_facet Hahnel, Antje
Wichmann, Henri
Greither, Thomas
Kappler, Matthias
Würl, Peter
Kotzsch, Matthias
Taubert, Helge
Vordermark, Dirk
Bache, Matthias
author_sort Hahnel, Antje
collection PubMed
description BACKGROUND: It is well known that osteopontin (OPN) plays an important role in tumor progression and that a high OPN expression level in several tumor entities correlates with poor prognosis in cancer patients. However, little is known about the prognostic relevance of the OPN mRNA splice variants. METHODS: We analyzed the mRNA expression levels of different OPN splice variants in tumor tissue of 124 soft tissue sarcoma (STS) patients. Quantitative real-time PCR (qRT-PCR) was used to analyze the mRNA expression level of three OPN splice variants (OPN-a, -b and -c). RESULTS: The multivariate Cox's proportional hazard regression model revealed that high mRNA expression levels of OPN splice variants are significantly associated with poor prognosis in STS patients (n = 124). Women (n = 68) with high mRNA expression levels of OPN-a and OPN-b have an especially elevated risk of tumor-related death (OPN-a: RR = 3.0, P = 0.01, CI = 1.3-6.8; OPN-b: RR = 3.4, P = 0.01, CI = 1.4-8.2). In particular, we found that high mRNA expression levels of OPN-b and OPN-c correlated with a high risk of tumor-related death in STS patients that received radiotherapy (n = 52; OPN-b: RR = 10.3, P < 0.01, CI = 2.0-53.7; OPN-c: RR = 11.4, P < 0.01, CI = 2.2-59.3). CONCLUSION: Our study shows that elevated mRNA expression levels of OPN splice variants are negative prognostic and predictive markers for STS patients. Further studies are needed to clarify the impact of the OPN splice variants on prognosis.
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spelling pubmed-33648732012-06-01 Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients Hahnel, Antje Wichmann, Henri Greither, Thomas Kappler, Matthias Würl, Peter Kotzsch, Matthias Taubert, Helge Vordermark, Dirk Bache, Matthias BMC Cancer Research Article BACKGROUND: It is well known that osteopontin (OPN) plays an important role in tumor progression and that a high OPN expression level in several tumor entities correlates with poor prognosis in cancer patients. However, little is known about the prognostic relevance of the OPN mRNA splice variants. METHODS: We analyzed the mRNA expression levels of different OPN splice variants in tumor tissue of 124 soft tissue sarcoma (STS) patients. Quantitative real-time PCR (qRT-PCR) was used to analyze the mRNA expression level of three OPN splice variants (OPN-a, -b and -c). RESULTS: The multivariate Cox's proportional hazard regression model revealed that high mRNA expression levels of OPN splice variants are significantly associated with poor prognosis in STS patients (n = 124). Women (n = 68) with high mRNA expression levels of OPN-a and OPN-b have an especially elevated risk of tumor-related death (OPN-a: RR = 3.0, P = 0.01, CI = 1.3-6.8; OPN-b: RR = 3.4, P = 0.01, CI = 1.4-8.2). In particular, we found that high mRNA expression levels of OPN-b and OPN-c correlated with a high risk of tumor-related death in STS patients that received radiotherapy (n = 52; OPN-b: RR = 10.3, P < 0.01, CI = 2.0-53.7; OPN-c: RR = 11.4, P < 0.01, CI = 2.2-59.3). CONCLUSION: Our study shows that elevated mRNA expression levels of OPN splice variants are negative prognostic and predictive markers for STS patients. Further studies are needed to clarify the impact of the OPN splice variants on prognosis. BioMed Central 2012-04-02 /pmc/articles/PMC3364873/ /pubmed/22471890 http://dx.doi.org/10.1186/1471-2407-12-131 Text en Copyright ©2012 Hahnel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hahnel, Antje
Wichmann, Henri
Greither, Thomas
Kappler, Matthias
Würl, Peter
Kotzsch, Matthias
Taubert, Helge
Vordermark, Dirk
Bache, Matthias
Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title_full Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title_fullStr Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title_full_unstemmed Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title_short Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
title_sort prognostic impact of mrna levels of osteopontin splice variants in soft tissue sarcoma patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364873/
https://www.ncbi.nlm.nih.gov/pubmed/22471890
http://dx.doi.org/10.1186/1471-2407-12-131
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