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AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival

Although CD44 was overexpressed and considered as a useful prognostic marker in renal cell carcinoma, the prognostic role of CD44s in clear cell renal cell carcinoma (ccRCC) remains controversial. Moreover, the correlation and prognostic significance of CD44s and its downstream signaling target pSTA...

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Autores principales: Qin, Jun, Yang, Bo, Qin, Wei-Jun, Wu, Guo-Jun, Shao, Chen, Xu, Bao-Qin, Yuan, Jian-Lin, Li, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708404/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s109
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author Qin, Jun
Yang, Bo
Qin, Wei-Jun
Wu, Guo-Jun
Shao, Chen
Xu, Bao-Qin
Yuan, Jian-Lin
Li, Ling
author_facet Qin, Jun
Yang, Bo
Qin, Wei-Jun
Wu, Guo-Jun
Shao, Chen
Xu, Bao-Qin
Yuan, Jian-Lin
Li, Ling
author_sort Qin, Jun
collection PubMed
description Although CD44 was overexpressed and considered as a useful prognostic marker in renal cell carcinoma, the prognostic role of CD44s in clear cell renal cell carcinoma (ccRCC) remains controversial. Moreover, the correlation and prognostic significance of CD44s and its downstream signaling target pSTAT3 are unclear in ccRCC. In this study, 75 pairs of carcinoma and paired adjacent non-tumor renal tissue samples were collected from patients with localized ccRCC who underwent a nephrectomy. The expression levels of CD44s and pSTAT3 were analyzed using immunohistochemistry. Correlations between CD44s/pSTAT3 expression and clinical and pathological characteristics were determined using χ test, Kaplan-Meier analysis and Cox’s proportional hazards model. We found that CD44s is highly expressed in 46.67% of tumor tissues, and its high expression was significantly associated with high tumor grade (P<0.001), large tumor size (P=0.009) and advanced T stage (P=0.004). A strong correlation exists between high expression of CD44s and pSTAT3 (r=0.4013, P=0.004). The joint over expression of CD44s and pSTAT3 was present in 42.66% of tumor specimens and had an additive negative impact on overall survival. Patients with CD44spSTAT3 expression had significantly poor survival as compared to patients with CD44spSTAT3 tumor expression (P=0.024), though the concurrent overexpression of CD44s and pSTAT3 was not an independent prognostic factor for overall survival. Our data indicate that expression of both CD44s and pSTAT3 in ccRCC is associated with advanced tumor stage and patient survival. The conclusions from this study may improve the prediction of ccRCC prognosis information when CD44s and pSTAT3 expression are evaluated together with classical clinicopathological parameters.
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spelling pubmed-47084042016-01-26 AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival Qin, Jun Yang, Bo Qin, Wei-Jun Wu, Guo-Jun Shao, Chen Xu, Bao-Qin Yuan, Jian-Lin Li, Ling Transl Androl Urol Abstract Publication Urology Although CD44 was overexpressed and considered as a useful prognostic marker in renal cell carcinoma, the prognostic role of CD44s in clear cell renal cell carcinoma (ccRCC) remains controversial. Moreover, the correlation and prognostic significance of CD44s and its downstream signaling target pSTAT3 are unclear in ccRCC. In this study, 75 pairs of carcinoma and paired adjacent non-tumor renal tissue samples were collected from patients with localized ccRCC who underwent a nephrectomy. The expression levels of CD44s and pSTAT3 were analyzed using immunohistochemistry. Correlations between CD44s/pSTAT3 expression and clinical and pathological characteristics were determined using χ test, Kaplan-Meier analysis and Cox’s proportional hazards model. We found that CD44s is highly expressed in 46.67% of tumor tissues, and its high expression was significantly associated with high tumor grade (P<0.001), large tumor size (P=0.009) and advanced T stage (P=0.004). A strong correlation exists between high expression of CD44s and pSTAT3 (r=0.4013, P=0.004). The joint over expression of CD44s and pSTAT3 was present in 42.66% of tumor specimens and had an additive negative impact on overall survival. Patients with CD44spSTAT3 expression had significantly poor survival as compared to patients with CD44spSTAT3 tumor expression (P=0.024), though the concurrent overexpression of CD44s and pSTAT3 was not an independent prognostic factor for overall survival. Our data indicate that expression of both CD44s and pSTAT3 in ccRCC is associated with advanced tumor stage and patient survival. The conclusions from this study may improve the prediction of ccRCC prognosis information when CD44s and pSTAT3 expression are evaluated together with classical clinicopathological parameters. AME Publishing Company 2014-09 /pmc/articles/PMC4708404/ http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s109 Text en 2014 Translational Andrology and Urology. All rights reserved.
spellingShingle Abstract Publication Urology
Qin, Jun
Yang, Bo
Qin, Wei-Jun
Wu, Guo-Jun
Shao, Chen
Xu, Bao-Qin
Yuan, Jian-Lin
Li, Ling
AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title_full AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title_fullStr AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title_full_unstemmed AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title_short AB109. Concurrent CD44s and STAT3 expression in human clear cell renal cellular carcinoma and its impact on survival
title_sort ab109. concurrent cd44s and stat3 expression in human clear cell renal cellular carcinoma and its impact on survival
topic Abstract Publication Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708404/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s109
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