Volume 23, Issue 3 685163 pp. 153-160
Article
Open Access

Overexpression of Fascin-1 in Advanced Colorectal Adenocarcinoma: Tissue Microarray Analysis of Immunostaining Scores with Clinicopathological Parameters

Wen-Chiuan Tsai

Wen-Chiuan Tsai

Department of Pathology Tri-Service General Hospital National Defense Medical Center Taipei, Taiwan , ndmctsgh.edu.tw

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You-Chen Chao

You-Chen Chao

Division of Gastroenterology Department of Internal Medicine Tri-Service General Hospital National Defense Medical Center Tapei, Taiwan , ndmctsgh.edu.tw

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Lai-Fa Sheu

Lai-Fa Sheu

Department of Pathology Tri-Service General Hospital National Defense Medical Center Taipei, Taiwan , ndmctsgh.edu.tw

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Junn-Liang Chang

Junn-Liang Chang

Department of Clinical Pathology and Laboratory Medicine Taoyuan Armed Forces General Hospital Lungtan Taoyuan County, Taiwan , aftygh.gov.tw

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Shin Nieh

Shin Nieh

Department of Pathology Tri-Service General Hospital National Defense Medical Center Taipei, Taiwan , ndmctsgh.edu.tw

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Jong-Shiaw Jin

Corresponding Author

Jong-Shiaw Jin

Department of Pathology Tri-Service General Hospital National Defense Medical Center Taipei, Taiwan , ndmctsgh.edu.tw

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First published: 06 June 2013
Citations: 26

Abstract

Objective: Fascin-1 is an actin-binding protein that promotes cell proliferation, adhesion and motility. We tested the hypothesis that fascin-1 expression correlates with clinicopathological parameters of colorectal adenocarcinomas.

Methods: Immunohistochemical analysis of fascin-1 was performed in tissue microarrays of 91 surgical specimens, including 32 well, 33 moderately, and 26 poorly differentiated colorectal adenocarcinomas; and in 22 specimens from colorectal adenomas with dysplasia.

Results: Scattered fascin-1 expression was demonstrated in 9 control specimens of normal colonic glandular epithelia. Higher fascin-1 immunostaining scores were significantly associated with advanced dysplasia in colorectal adenomas (mild 4.2 ± 1.3, moderate 13.5 ± 5.3, and severe 22.5 ± 6.7) and high-grade histopathological differentiation of colorectal adenocarcinomas (grade I 88.6 ± 9, grade II 101 ± 11, and grade III 144 ± 13). Higher immunostaining scores of fascin-1 were also significantly associated with advanced T stage (T1: 42 ± 10, T2: 60 ± 12, T3: 108 ± 12, and T4: 142 ± 15). Higher fascin-1 scores were related with more advanced M and N stages of colorectal carcinomas, but not significant correlation.

Conclusions: Higher expression of fascin-1 correlates significantly with tumor grades and TNM stages in colorectal adenocarcinomas and also with levels of dysplastic change in colorectal adenomas.

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