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Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma

BACKGROUND: Fascin and CD44v6 may have significant roles as biomarkers in tumour progression and metastasis. In endometrioid carcinomas, the fascin expression profile is less defined, and the significance of CD44v6 is uncertain. We aimed to investigate the expressions of both fascin and CD44v6 in en...

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Autores principales: Gun, Banu Dogan, Bahadir, Burak, Bektas, Sibel, Barut, Figen, Yurdakan, Gamze, Kandemir, Nilufer Onak, Ozdamar, Sukru Oguz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407727/
https://www.ncbi.nlm.nih.gov/pubmed/22784357
http://dx.doi.org/10.1186/1746-1596-7-80
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author Gun, Banu Dogan
Bahadir, Burak
Bektas, Sibel
Barut, Figen
Yurdakan, Gamze
Kandemir, Nilufer Onak
Ozdamar, Sukru Oguz
author_facet Gun, Banu Dogan
Bahadir, Burak
Bektas, Sibel
Barut, Figen
Yurdakan, Gamze
Kandemir, Nilufer Onak
Ozdamar, Sukru Oguz
author_sort Gun, Banu Dogan
collection PubMed
description BACKGROUND: Fascin and CD44v6 may have significant roles as biomarkers in tumour progression and metastasis. In endometrioid carcinomas, the fascin expression profile is less defined, and the significance of CD44v6 is uncertain. We aimed to investigate the expressions of both fascin and CD44v6 in endometrioid carcinomas and to evaluate their inter-relation with clinicopathological parameters. METHODS: Fascin and CD44v6 expressions were evaluated, individually and in combination, in a series of 47 endometrioid carcinomas and 10 proliferative endometrium samples. The staining extent and intensity of both markers in tumour cells were scored semiquantitatively. The relationship between immunoexpressions and clinicopathological variables was assessed. RESULTS: The expression rates of fascin and CD44v6 in endometrioid carcinoma were 72.34% and 46.80%, respectively. Although these expression rates were higher than those in proliferative endometrial samples, fascin expression showed a statistically significant difference from the normal group (p = 0.02), but CD44v6 did not differ (p = 0.54). Fascin expression was significantly correlated with tumour grade (p = 0.003) and neural invasion (p = 0.036) in a univariate analysis. In contrast, no significant correlation was found between CD44v6 and any of the clinicopathological parameters. CONCLUSIONS: Our findings suggest that fascin might be an independent prognostic indicator in the different steps of extracellular matrix invasion. On the other hand, CD44v6 was not a predictive factor in endometrioid cancer. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/8511594927206899.
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spelling pubmed-34077272012-07-30 Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma Gun, Banu Dogan Bahadir, Burak Bektas, Sibel Barut, Figen Yurdakan, Gamze Kandemir, Nilufer Onak Ozdamar, Sukru Oguz Diagn Pathol Research BACKGROUND: Fascin and CD44v6 may have significant roles as biomarkers in tumour progression and metastasis. In endometrioid carcinomas, the fascin expression profile is less defined, and the significance of CD44v6 is uncertain. We aimed to investigate the expressions of both fascin and CD44v6 in endometrioid carcinomas and to evaluate their inter-relation with clinicopathological parameters. METHODS: Fascin and CD44v6 expressions were evaluated, individually and in combination, in a series of 47 endometrioid carcinomas and 10 proliferative endometrium samples. The staining extent and intensity of both markers in tumour cells were scored semiquantitatively. The relationship between immunoexpressions and clinicopathological variables was assessed. RESULTS: The expression rates of fascin and CD44v6 in endometrioid carcinoma were 72.34% and 46.80%, respectively. Although these expression rates were higher than those in proliferative endometrial samples, fascin expression showed a statistically significant difference from the normal group (p = 0.02), but CD44v6 did not differ (p = 0.54). Fascin expression was significantly correlated with tumour grade (p = 0.003) and neural invasion (p = 0.036) in a univariate analysis. In contrast, no significant correlation was found between CD44v6 and any of the clinicopathological parameters. CONCLUSIONS: Our findings suggest that fascin might be an independent prognostic indicator in the different steps of extracellular matrix invasion. On the other hand, CD44v6 was not a predictive factor in endometrioid cancer. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/8511594927206899. BioMed Central 2012-07-11 /pmc/articles/PMC3407727/ /pubmed/22784357 http://dx.doi.org/10.1186/1746-1596-7-80 Text en Copyright ©2012 Gun 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
Gun, Banu Dogan
Bahadir, Burak
Bektas, Sibel
Barut, Figen
Yurdakan, Gamze
Kandemir, Nilufer Onak
Ozdamar, Sukru Oguz
Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title_full Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title_fullStr Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title_full_unstemmed Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title_short Clinicopathological significance of fascin and CD44v6 expression in endometrioid carcinoma
title_sort clinicopathological significance of fascin and cd44v6 expression in endometrioid carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407727/
https://www.ncbi.nlm.nih.gov/pubmed/22784357
http://dx.doi.org/10.1186/1746-1596-7-80
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