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Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis
BACKGROUND: Interferon-α (IFN-α) is one of the central agents in immunotherapy for renal cell carcinoma (RCC) and binds to the IFN-α receptor (IFNAR). We investigated the role of IFNAR in RCC. METHODS: We quantified IFNAR mRNA expression in paired tumor and non-tumor samples from the surgical specim...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1988828/ https://www.ncbi.nlm.nih.gov/pubmed/17697365 http://dx.doi.org/10.1186/1471-2407-7-159 |
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author | Kamai, Takao Yanai, Yoshiaki Arai, Kyoko Abe, Hideyuki Yamanishi, Tomonori Kurimoto, Masashi Yoshida, Ken-Ichiro |
author_facet | Kamai, Takao Yanai, Yoshiaki Arai, Kyoko Abe, Hideyuki Yamanishi, Tomonori Kurimoto, Masashi Yoshida, Ken-Ichiro |
author_sort | Kamai, Takao |
collection | PubMed |
description | BACKGROUND: Interferon-α (IFN-α) is one of the central agents in immunotherapy for renal cell carcinoma (RCC) and binds to the IFN-α receptor (IFNAR). We investigated the role of IFNAR in RCC. METHODS: We quantified IFNAR mRNA expression in paired tumor and non-tumor samples from the surgical specimens of 103 consecutive patients with RCC using a real-time reverse transcription polymerase chain reaction (RT-PCR), and IFNAR2 protein using Western blotting. RESULTS: The absolute level of IFNAR1 and IFNAR2 mRNAs in tumor and non-tumor tissues did not correlate with the malignant and metastatic profiles. The relative yields of the PCR product from the tumor tissue to that from the corresponding non-tumor tissue (T/N) for the expression of IFNAR mRNAs were calculated. While the T/N ratio of IFNAR1 did not correlate with any factor, a high T/N ratio of IFNAR2 correlated with poor differentiation (P < 0.05), local invasion (P < 0.001), and metastasis (P < 0.0001). By multivariate analysis, a high T/N ratio of IFNAR2 predicted a shortened overall survival in all cases (P < 0.05) and a shorter disease-free survival in those without metastasis (M0; 68 cases, P < 0.05). Impressively, patients with a poorer response to IFN-α treatment had a higher IFNAR2 T/N ratio than those who had a good response (P < 0.05). IFNAR2c protein expression was higher in the primary tumors in patients with metastases (M1; 35 cases) compared to those without ( P < 0.0001). CONCLUSION: IFNAR2 is associated with the progression of RCC. |
format | Text |
id | pubmed-1988828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-19888282007-09-21 Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis Kamai, Takao Yanai, Yoshiaki Arai, Kyoko Abe, Hideyuki Yamanishi, Tomonori Kurimoto, Masashi Yoshida, Ken-Ichiro BMC Cancer Research Article BACKGROUND: Interferon-α (IFN-α) is one of the central agents in immunotherapy for renal cell carcinoma (RCC) and binds to the IFN-α receptor (IFNAR). We investigated the role of IFNAR in RCC. METHODS: We quantified IFNAR mRNA expression in paired tumor and non-tumor samples from the surgical specimens of 103 consecutive patients with RCC using a real-time reverse transcription polymerase chain reaction (RT-PCR), and IFNAR2 protein using Western blotting. RESULTS: The absolute level of IFNAR1 and IFNAR2 mRNAs in tumor and non-tumor tissues did not correlate with the malignant and metastatic profiles. The relative yields of the PCR product from the tumor tissue to that from the corresponding non-tumor tissue (T/N) for the expression of IFNAR mRNAs were calculated. While the T/N ratio of IFNAR1 did not correlate with any factor, a high T/N ratio of IFNAR2 correlated with poor differentiation (P < 0.05), local invasion (P < 0.001), and metastasis (P < 0.0001). By multivariate analysis, a high T/N ratio of IFNAR2 predicted a shortened overall survival in all cases (P < 0.05) and a shorter disease-free survival in those without metastasis (M0; 68 cases, P < 0.05). Impressively, patients with a poorer response to IFN-α treatment had a higher IFNAR2 T/N ratio than those who had a good response (P < 0.05). IFNAR2c protein expression was higher in the primary tumors in patients with metastases (M1; 35 cases) compared to those without ( P < 0.0001). CONCLUSION: IFNAR2 is associated with the progression of RCC. BioMed Central 2007-08-15 /pmc/articles/PMC1988828/ /pubmed/17697365 http://dx.doi.org/10.1186/1471-2407-7-159 Text en Copyright © 2007 Kamai 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 Kamai, Takao Yanai, Yoshiaki Arai, Kyoko Abe, Hideyuki Yamanishi, Tomonori Kurimoto, Masashi Yoshida, Ken-Ichiro Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title | Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title_full | Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title_fullStr | Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title_full_unstemmed | Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title_short | Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis |
title_sort | increased interferon alpha receptor 2 mrna levels is associated with renal cell carcinoma metastasis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1988828/ https://www.ncbi.nlm.nih.gov/pubmed/17697365 http://dx.doi.org/10.1186/1471-2407-7-159 |
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