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Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2

We performed gene expression profiling in bladder cancer patients to identify cancer-specific survival-related genes in muscle invasive bladder cancer (MIBC) patients. Sixty-two patients with MIBC were selected as the original cohort and another 118 MIBC patients were chosen as a validation cohort....

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Autores principales: Kim, Ye-Hwan, Kim, Won Tae, Jeong, Pildu, Ha, Yun-Sok, Kang, Ho Won, Yun, Seok Joong, Moon, Sung-Kwon, Choi, Yung Hyun, Kim, Isaac Yi, Kim, Wun-Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945129/
https://www.ncbi.nlm.nih.gov/pubmed/24616583
http://dx.doi.org/10.3346/jkms.2014.29.3.351
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author Kim, Ye-Hwan
Kim, Won Tae
Jeong, Pildu
Ha, Yun-Sok
Kang, Ho Won
Yun, Seok Joong
Moon, Sung-Kwon
Choi, Yung Hyun
Kim, Isaac Yi
Kim, Wun-Jae
author_facet Kim, Ye-Hwan
Kim, Won Tae
Jeong, Pildu
Ha, Yun-Sok
Kang, Ho Won
Yun, Seok Joong
Moon, Sung-Kwon
Choi, Yung Hyun
Kim, Isaac Yi
Kim, Wun-Jae
author_sort Kim, Ye-Hwan
collection PubMed
description We performed gene expression profiling in bladder cancer patients to identify cancer-specific survival-related genes in muscle invasive bladder cancer (MIBC) patients. Sixty-two patients with MIBC were selected as the original cohort and another 118 MIBC patients were chosen as a validation cohort. The expression of USP18, DGCR2, and ZNF699 genes were measured and we analyzed the association between gene signatures and survival. USP18 and DGCR2, were significantly correlated to cancer-specific death (P=0.020, P=0.007, respectively). Cancer-specific survival in the low USP18 or DGCR2 expression group was significantly longer than the high expression group (P=0.018, P=0.006, respectively). In multivariate Cox regression analysis, a combination of USP18 and DGCR2 mRNA expression levels were significant risk factors for cancer-specific death (HR, 2.106; CI, 1.043-4.254, P=0.038). Overall survival and cancer-specific survival rates in the low-combination group were significantly longer than those in the high-expression group (P=0.001, both). In conclusion, decreased expressions of USP18 and DGCR2 were significantly associated with longer cancer-specific survival, and also the combination of two genes was correlated to a longer survival for MIBC patients. Thus, the combination of USP18 and DGCR2 expression was shown to be a reliable prognostic marker for cancer-specific survival in MIBC. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-39451292014-03-10 Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2 Kim, Ye-Hwan Kim, Won Tae Jeong, Pildu Ha, Yun-Sok Kang, Ho Won Yun, Seok Joong Moon, Sung-Kwon Choi, Yung Hyun Kim, Isaac Yi Kim, Wun-Jae J Korean Med Sci Original Article We performed gene expression profiling in bladder cancer patients to identify cancer-specific survival-related genes in muscle invasive bladder cancer (MIBC) patients. Sixty-two patients with MIBC were selected as the original cohort and another 118 MIBC patients were chosen as a validation cohort. The expression of USP18, DGCR2, and ZNF699 genes were measured and we analyzed the association between gene signatures and survival. USP18 and DGCR2, were significantly correlated to cancer-specific death (P=0.020, P=0.007, respectively). Cancer-specific survival in the low USP18 or DGCR2 expression group was significantly longer than the high expression group (P=0.018, P=0.006, respectively). In multivariate Cox regression analysis, a combination of USP18 and DGCR2 mRNA expression levels were significant risk factors for cancer-specific death (HR, 2.106; CI, 1.043-4.254, P=0.038). Overall survival and cancer-specific survival rates in the low-combination group were significantly longer than those in the high-expression group (P=0.001, both). In conclusion, decreased expressions of USP18 and DGCR2 were significantly associated with longer cancer-specific survival, and also the combination of two genes was correlated to a longer survival for MIBC patients. Thus, the combination of USP18 and DGCR2 expression was shown to be a reliable prognostic marker for cancer-specific survival in MIBC. GRAPHICAL ABSTRACT: [Image: see text] The Korean Academy of Medical Sciences 2014-03 2014-02-27 /pmc/articles/PMC3945129/ /pubmed/24616583 http://dx.doi.org/10.3346/jkms.2014.29.3.351 Text en © 2014 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Ye-Hwan
Kim, Won Tae
Jeong, Pildu
Ha, Yun-Sok
Kang, Ho Won
Yun, Seok Joong
Moon, Sung-Kwon
Choi, Yung Hyun
Kim, Isaac Yi
Kim, Wun-Jae
Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title_full Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title_fullStr Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title_full_unstemmed Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title_short Novel Combination Markers for Predicting Survival in Patients with Muscle Invasive Bladder Cancer: USP18 and DGCR2
title_sort novel combination markers for predicting survival in patients with muscle invasive bladder cancer: usp18 and dgcr2
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945129/
https://www.ncbi.nlm.nih.gov/pubmed/24616583
http://dx.doi.org/10.3346/jkms.2014.29.3.351
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