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A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma

BACKGROUND: Accurate prediction of the prognosis of RCC using a single biomarker is challenging due to the genetic heterogeneity of the disease. However, it is essential to develop an accurate system to allow better patient selection for optimal treatment strategies. ARL4C, ECT2, SOD2, and STEAP3 ar...

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Autores principales: Kubota, Shigehisa, Yoshida, Tetsuya, Kageyama, Susumu, Isono, Takahiro, Yuasa, Takeshi, Yonese, Junji, Kushima, Ryoji, Kawauchi, Akihiro, Chano, Tokuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584101/
https://www.ncbi.nlm.nih.gov/pubmed/33092599
http://dx.doi.org/10.1186/s12957-020-02046-9
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author Kubota, Shigehisa
Yoshida, Tetsuya
Kageyama, Susumu
Isono, Takahiro
Yuasa, Takeshi
Yonese, Junji
Kushima, Ryoji
Kawauchi, Akihiro
Chano, Tokuhiro
author_facet Kubota, Shigehisa
Yoshida, Tetsuya
Kageyama, Susumu
Isono, Takahiro
Yuasa, Takeshi
Yonese, Junji
Kushima, Ryoji
Kawauchi, Akihiro
Chano, Tokuhiro
author_sort Kubota, Shigehisa
collection PubMed
description BACKGROUND: Accurate prediction of the prognosis of RCC using a single biomarker is challenging due to the genetic heterogeneity of the disease. However, it is essential to develop an accurate system to allow better patient selection for optimal treatment strategies. ARL4C, ECT2, SOD2, and STEAP3 are novel molecular biomarkers identified in earlier studies as survival-related genes by comprehensive analyses of 43 primary RCC tissues and RCC cell lines. METHODS: To develop a prognostic model based on these multiple biomarkers, the expression of four biomarkers ARL4C, ECT2, SOD2, and STEAP3 in primary RCC tissue were semi-quantitatively investigated by immunohistochemical analysis in an independent cohort of 97 patients who underwent nephrectomy, and the clinical significance of these biomarkers were analyzed by survival analysis using Kaplan-Meier curves. The prognostic model was constructed by calculation of the contribution score to prognosis of each biomarker on Cox regression analysis, and its prognostic performance was validated. RESULTS: Patients whose tumors had high expression of the individual biomarkers had shorter cancer-specific survival (CSS) from the time of primary nephrectomy. The prognostic model based on four biomarkers segregated the patients into a high- and low-risk scored group according to defined cut-off value. This approach was more robust in predicting CSS compared to each single biomarker alone in the total of 97 patients with RCC. Especially in the 36 metastatic RCC patients, our prognostic model could more accurately predict early events within 2 years of diagnosis of metastasis. In addition, high risk-scored patients with particular strong SOD2 expression had a much worse prognosis in 25 patients with metastatic RCC who were treated with molecular targeting agents. CONCLUSIONS: Our findings indicate that a prognostic model based on four novel biomarkers provides valuable data for prediction of clinical prognosis and useful information for considering the follow-up conditions and therapeutic strategies for patients with primary and metastatic RCC.
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spelling pubmed-75841012020-10-26 A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma Kubota, Shigehisa Yoshida, Tetsuya Kageyama, Susumu Isono, Takahiro Yuasa, Takeshi Yonese, Junji Kushima, Ryoji Kawauchi, Akihiro Chano, Tokuhiro World J Surg Oncol Research BACKGROUND: Accurate prediction of the prognosis of RCC using a single biomarker is challenging due to the genetic heterogeneity of the disease. However, it is essential to develop an accurate system to allow better patient selection for optimal treatment strategies. ARL4C, ECT2, SOD2, and STEAP3 are novel molecular biomarkers identified in earlier studies as survival-related genes by comprehensive analyses of 43 primary RCC tissues and RCC cell lines. METHODS: To develop a prognostic model based on these multiple biomarkers, the expression of four biomarkers ARL4C, ECT2, SOD2, and STEAP3 in primary RCC tissue were semi-quantitatively investigated by immunohistochemical analysis in an independent cohort of 97 patients who underwent nephrectomy, and the clinical significance of these biomarkers were analyzed by survival analysis using Kaplan-Meier curves. The prognostic model was constructed by calculation of the contribution score to prognosis of each biomarker on Cox regression analysis, and its prognostic performance was validated. RESULTS: Patients whose tumors had high expression of the individual biomarkers had shorter cancer-specific survival (CSS) from the time of primary nephrectomy. The prognostic model based on four biomarkers segregated the patients into a high- and low-risk scored group according to defined cut-off value. This approach was more robust in predicting CSS compared to each single biomarker alone in the total of 97 patients with RCC. Especially in the 36 metastatic RCC patients, our prognostic model could more accurately predict early events within 2 years of diagnosis of metastasis. In addition, high risk-scored patients with particular strong SOD2 expression had a much worse prognosis in 25 patients with metastatic RCC who were treated with molecular targeting agents. CONCLUSIONS: Our findings indicate that a prognostic model based on four novel biomarkers provides valuable data for prediction of clinical prognosis and useful information for considering the follow-up conditions and therapeutic strategies for patients with primary and metastatic RCC. BioMed Central 2020-10-22 /pmc/articles/PMC7584101/ /pubmed/33092599 http://dx.doi.org/10.1186/s12957-020-02046-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kubota, Shigehisa
Yoshida, Tetsuya
Kageyama, Susumu
Isono, Takahiro
Yuasa, Takeshi
Yonese, Junji
Kushima, Ryoji
Kawauchi, Akihiro
Chano, Tokuhiro
A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title_full A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title_fullStr A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title_full_unstemmed A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title_short A risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
title_sort risk stratification model based on four novel biomarkers predicts prognosis for patients with renal cell carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584101/
https://www.ncbi.nlm.nih.gov/pubmed/33092599
http://dx.doi.org/10.1186/s12957-020-02046-9
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