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Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival

BACKGROUND: Raf-1 kinase inhibitor protein (RKIP) has been reported to negatively regulate signal kinases of major survival pathways. RKIP activity is modulated in part by phosphorylation on Serine 153 by protein kinase C, which leads to dissociation of RKIP from Raf-1. RKIP expression is low in man...

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Autores principales: Huerta-Yepez, Sara, Yoon, Nam K, Hernandez-Cueto, Angeles, Mah, Vei, Rivera-Pazos, Clara M, Chatterjee, Devasis, Vega, Mario I, Maresh, Erin L, Horvath, Steve, Chia, David, Bonavida, Benjamin, Goodglick, Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134426/
https://www.ncbi.nlm.nih.gov/pubmed/21689459
http://dx.doi.org/10.1186/1471-2407-11-259
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author Huerta-Yepez, Sara
Yoon, Nam K
Hernandez-Cueto, Angeles
Mah, Vei
Rivera-Pazos, Clara M
Chatterjee, Devasis
Vega, Mario I
Maresh, Erin L
Horvath, Steve
Chia, David
Bonavida, Benjamin
Goodglick, Lee
author_facet Huerta-Yepez, Sara
Yoon, Nam K
Hernandez-Cueto, Angeles
Mah, Vei
Rivera-Pazos, Clara M
Chatterjee, Devasis
Vega, Mario I
Maresh, Erin L
Horvath, Steve
Chia, David
Bonavida, Benjamin
Goodglick, Lee
author_sort Huerta-Yepez, Sara
collection PubMed
description BACKGROUND: Raf-1 kinase inhibitor protein (RKIP) has been reported to negatively regulate signal kinases of major survival pathways. RKIP activity is modulated in part by phosphorylation on Serine 153 by protein kinase C, which leads to dissociation of RKIP from Raf-1. RKIP expression is low in many human cancers and represents an indicator of poor prognosis and/or induction of metastasis. The prognostic power has typically been based on total RKIP expression and has not considered the significance of phospho-RKIP. METHODS: The present study examined the expression levels of both RKIP and phospho-RKIP in human lung cancer tissue microarray proteomics technology. RESULTS: Total RKIP and phospho-RKIP expression levels were similar in normal and cancerous tissues. phospho-RKIP levels slightly decreased in metastatic lesions. However, the expression levels of phospho-RKIP, in contrast to total RKIP, displayed significant predictive power for outcome with normal expression of phospho-RKIP predicting a more favorable survival compared to lower levels (P = 0.0118); this was even more pronounced in more senior individuals and in those with early stage lung cancer. CONCLUSIONS: This study examines for the first time, the expression profile of RKIP and phospho-RKIP in lung cancer. Significantly, we found that phospho-RKIP was a predictive indicator of survival.
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spelling pubmed-31344262011-07-13 Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival Huerta-Yepez, Sara Yoon, Nam K Hernandez-Cueto, Angeles Mah, Vei Rivera-Pazos, Clara M Chatterjee, Devasis Vega, Mario I Maresh, Erin L Horvath, Steve Chia, David Bonavida, Benjamin Goodglick, Lee BMC Cancer Research Article BACKGROUND: Raf-1 kinase inhibitor protein (RKIP) has been reported to negatively regulate signal kinases of major survival pathways. RKIP activity is modulated in part by phosphorylation on Serine 153 by protein kinase C, which leads to dissociation of RKIP from Raf-1. RKIP expression is low in many human cancers and represents an indicator of poor prognosis and/or induction of metastasis. The prognostic power has typically been based on total RKIP expression and has not considered the significance of phospho-RKIP. METHODS: The present study examined the expression levels of both RKIP and phospho-RKIP in human lung cancer tissue microarray proteomics technology. RESULTS: Total RKIP and phospho-RKIP expression levels were similar in normal and cancerous tissues. phospho-RKIP levels slightly decreased in metastatic lesions. However, the expression levels of phospho-RKIP, in contrast to total RKIP, displayed significant predictive power for outcome with normal expression of phospho-RKIP predicting a more favorable survival compared to lower levels (P = 0.0118); this was even more pronounced in more senior individuals and in those with early stage lung cancer. CONCLUSIONS: This study examines for the first time, the expression profile of RKIP and phospho-RKIP in lung cancer. Significantly, we found that phospho-RKIP was a predictive indicator of survival. BioMed Central 2011-06-21 /pmc/articles/PMC3134426/ /pubmed/21689459 http://dx.doi.org/10.1186/1471-2407-11-259 Text en Copyright ©2011 Huerta-Yepez 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
Huerta-Yepez, Sara
Yoon, Nam K
Hernandez-Cueto, Angeles
Mah, Vei
Rivera-Pazos, Clara M
Chatterjee, Devasis
Vega, Mario I
Maresh, Erin L
Horvath, Steve
Chia, David
Bonavida, Benjamin
Goodglick, Lee
Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title_full Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title_fullStr Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title_full_unstemmed Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title_short Expression of phosphorylated raf kinase inhibitor protein (pRKIP) is a predictor of lung cancer survival
title_sort expression of phosphorylated raf kinase inhibitor protein (prkip) is a predictor of lung cancer survival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134426/
https://www.ncbi.nlm.nih.gov/pubmed/21689459
http://dx.doi.org/10.1186/1471-2407-11-259
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