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PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer

BACKGROUND: To date individual markers have failed to correctly predict resistance against anticancer agents in breast cancer. We used gene expression patterns attributable to chemotherapy-resistant cells to detect potential new biomarkers related to anthracycline resistance. One of the genes, PSMB7...

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Autores principales: Munkácsy, G, Abdul-Ghani, R, Mihály, Z, Tegze, B, Tchernitsa, O, Surowiak, P, Schäfer, R, Györffy, B
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816652/
https://www.ncbi.nlm.nih.gov/pubmed/20010949
http://dx.doi.org/10.1038/sj.bjc.6605478
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author Munkácsy, G
Abdul-Ghani, R
Mihály, Z
Tegze, B
Tchernitsa, O
Surowiak, P
Schäfer, R
Györffy, B
author_facet Munkácsy, G
Abdul-Ghani, R
Mihály, Z
Tegze, B
Tchernitsa, O
Surowiak, P
Schäfer, R
Györffy, B
author_sort Munkácsy, G
collection PubMed
description BACKGROUND: To date individual markers have failed to correctly predict resistance against anticancer agents in breast cancer. We used gene expression patterns attributable to chemotherapy-resistant cells to detect potential new biomarkers related to anthracycline resistance. One of the genes, PSMB7, was selected for further functional studies and clinical validation. METHODS: We contrasted the expression profiles of four pairs of different human tumour cell lines and of their counterparts resistant to doxorubicin. Observed overexpression of PSMB7 in resistant cell lines was validated by immunohistochemistry. To examine its function in chemoresistance, we silenced the gene by RNA interference (RNAi) in doxorubicin-resistant MCF-7 breast cancer cells, then cell vitality was measured after doxorubicin treatment. Microarray gene expression from GEO raw microarray samples with available progression-free survival data was downloaded, and expression of PSMB7 was used for grouping samples. RESULTS: After doxorubicin treatment, 79.8±13.3% of resistant cells survived. Silencing of PSMB7 in resistant cells decreased survival to 31.8±6.4% (P>0.001). A similar effect was observed after paclitaxel treatment. In 1592 microarray samples, the patients with high PSMB7 expression had a significantly shorter survival than the patients with low expression (P<0.001). CONCLUSION: Our findings suggest that high PSMB7 expression is an unfavourable prognostic marker in breast cancer.
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spelling pubmed-28166522011-01-19 PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer Munkácsy, G Abdul-Ghani, R Mihály, Z Tegze, B Tchernitsa, O Surowiak, P Schäfer, R Györffy, B Br J Cancer Molecular Diagnostics BACKGROUND: To date individual markers have failed to correctly predict resistance against anticancer agents in breast cancer. We used gene expression patterns attributable to chemotherapy-resistant cells to detect potential new biomarkers related to anthracycline resistance. One of the genes, PSMB7, was selected for further functional studies and clinical validation. METHODS: We contrasted the expression profiles of four pairs of different human tumour cell lines and of their counterparts resistant to doxorubicin. Observed overexpression of PSMB7 in resistant cell lines was validated by immunohistochemistry. To examine its function in chemoresistance, we silenced the gene by RNA interference (RNAi) in doxorubicin-resistant MCF-7 breast cancer cells, then cell vitality was measured after doxorubicin treatment. Microarray gene expression from GEO raw microarray samples with available progression-free survival data was downloaded, and expression of PSMB7 was used for grouping samples. RESULTS: After doxorubicin treatment, 79.8±13.3% of resistant cells survived. Silencing of PSMB7 in resistant cells decreased survival to 31.8±6.4% (P>0.001). A similar effect was observed after paclitaxel treatment. In 1592 microarray samples, the patients with high PSMB7 expression had a significantly shorter survival than the patients with low expression (P<0.001). CONCLUSION: Our findings suggest that high PSMB7 expression is an unfavourable prognostic marker in breast cancer. Nature Publishing Group 2010-01-19 2009-12-15 /pmc/articles/PMC2816652/ /pubmed/20010949 http://dx.doi.org/10.1038/sj.bjc.6605478 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Munkácsy, G
Abdul-Ghani, R
Mihály, Z
Tegze, B
Tchernitsa, O
Surowiak, P
Schäfer, R
Györffy, B
PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title_full PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title_fullStr PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title_full_unstemmed PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title_short PSMB7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
title_sort psmb7 is associated with anthracycline resistance and is a prognostic biomarker in breast cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816652/
https://www.ncbi.nlm.nih.gov/pubmed/20010949
http://dx.doi.org/10.1038/sj.bjc.6605478
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