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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....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3364873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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