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Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma
BACKGROUND AND PURPOSE: A previous study demonstrated that GALNT10 affects the sensitivity of cancer cells to tyrosine kinase inhibitor (TKI) therapy. The aim of this study was to assess whether GALNT10 holds a prognostic role in metastatic renal cell carcinoma (mRCC) patients treated with TKI agent...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362461/ https://www.ncbi.nlm.nih.gov/pubmed/28122358 http://dx.doi.org/10.18632/oncotarget.14786 |
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author | Liu, Li Xiong, Ying Xi, Wei Wang, Jiajun Qu, Yang Lin, Zhiyuan Chen, Xiang Yao, Jiaxi Xu, Jiejie Guo, Jianming |
author_facet | Liu, Li Xiong, Ying Xi, Wei Wang, Jiajun Qu, Yang Lin, Zhiyuan Chen, Xiang Yao, Jiaxi Xu, Jiejie Guo, Jianming |
author_sort | Liu, Li |
collection | PubMed |
description | BACKGROUND AND PURPOSE: A previous study demonstrated that GALNT10 affects the sensitivity of cancer cells to tyrosine kinase inhibitor (TKI) therapy. The aim of this study was to assess whether GALNT10 holds a prognostic role in metastatic renal cell carcinoma (mRCC) patients treated with TKI agents. RESULTS: GALNT10 had no statistical correlation with any other clinicopathological parameters except for route of gaining samples (P = 0.001) and Heng's risk stratification (P = 0.011). Patients with high level of GALNT10 had significantly shorter overall survival (OS) (P < 0.001) and progression-free survival (PFS) (P = 0.002). Importantly, this relationship existed in OS and PFS analyses in sunitinib-treated patients and in OS analyses in sorafenib-treated patients (P = 0.024). In contrast to sorafenib group, percentage of partial response (PR) and stable disease (SD) were higher in sunitinib group, while percentage of progression disease (PD) was much lower. Univariate and multivariate analyses identified that GALNT10 was an independent prognostic factor for OS (HR = 1.938, P = 0.014), not for PFS (HR = 1.532, P = 0.065), in mRCC. Incorporating it into Heng's risk model could sharpen its efficacy in distinguishing patients with potential higher risk. MATERIALS AND METHODS: We retrospectively enrolled 138 mRCC patients treated with sunitinib or sorafenib at Zhongshan Hospital, Shanghai, China. A total of 111 valid cases were finally applied for analyses. CONCLUSIONS: These findings suggest that GALNT10 could be applied as a prognostic marker for OS in mRCC patients. |
format | Online Article Text |
id | pubmed-5362461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53624612017-04-24 Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma Liu, Li Xiong, Ying Xi, Wei Wang, Jiajun Qu, Yang Lin, Zhiyuan Chen, Xiang Yao, Jiaxi Xu, Jiejie Guo, Jianming Oncotarget Research Paper BACKGROUND AND PURPOSE: A previous study demonstrated that GALNT10 affects the sensitivity of cancer cells to tyrosine kinase inhibitor (TKI) therapy. The aim of this study was to assess whether GALNT10 holds a prognostic role in metastatic renal cell carcinoma (mRCC) patients treated with TKI agents. RESULTS: GALNT10 had no statistical correlation with any other clinicopathological parameters except for route of gaining samples (P = 0.001) and Heng's risk stratification (P = 0.011). Patients with high level of GALNT10 had significantly shorter overall survival (OS) (P < 0.001) and progression-free survival (PFS) (P = 0.002). Importantly, this relationship existed in OS and PFS analyses in sunitinib-treated patients and in OS analyses in sorafenib-treated patients (P = 0.024). In contrast to sorafenib group, percentage of partial response (PR) and stable disease (SD) were higher in sunitinib group, while percentage of progression disease (PD) was much lower. Univariate and multivariate analyses identified that GALNT10 was an independent prognostic factor for OS (HR = 1.938, P = 0.014), not for PFS (HR = 1.532, P = 0.065), in mRCC. Incorporating it into Heng's risk model could sharpen its efficacy in distinguishing patients with potential higher risk. MATERIALS AND METHODS: We retrospectively enrolled 138 mRCC patients treated with sunitinib or sorafenib at Zhongshan Hospital, Shanghai, China. A total of 111 valid cases were finally applied for analyses. CONCLUSIONS: These findings suggest that GALNT10 could be applied as a prognostic marker for OS in mRCC patients. Impact Journals LLC 2017-01-21 /pmc/articles/PMC5362461/ /pubmed/28122358 http://dx.doi.org/10.18632/oncotarget.14786 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Li Xiong, Ying Xi, Wei Wang, Jiajun Qu, Yang Lin, Zhiyuan Chen, Xiang Yao, Jiaxi Xu, Jiejie Guo, Jianming Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title | Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title_full | Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title_fullStr | Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title_full_unstemmed | Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title_short | Prognostic role of N-Acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
title_sort | prognostic role of n-acetylgalactosaminyltransferase 10 in metastatic renal cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362461/ https://www.ncbi.nlm.nih.gov/pubmed/28122358 http://dx.doi.org/10.18632/oncotarget.14786 |
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