Abstract | BACKGROUND: MATERIALS AND METHODS: This study performed immunohistochemistry in tissue microarrays, profiling premalignant lesions and invasive tumors. RESULTS:
Fascin increased across the following states as follows: normal-appearing epithelium (26%) to dysplasia (46%) to ESCC (68%), while CK4 was undetectable in ESCC (0%) compared to normal-appearing epithelium (45%) or dysplasia (41%). CK14 was elevated and invariant in expression. In regression analyses, compared to normal-appearing epithelium, higher fascin expression was associated with a 36% increased risk of dysplasia (odds ratio=1.36) and a 56% increased risk of invasive ESCC (odds ratio=1.56). CONCLUSION: Expression of fascin is up-regulated in the transformation from normal-appearing epithelium, through dysplasia, into invasive carcinoma. Expression of CK4, CK14 and fascin did not correlate with patient survival. Fascin has a potential role as an early detection biomarker and CK4 as a tumor marker in ESCC.
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Authors | Mikiko Takikita, Nan Hu, Jian-Zhong Shou, Carol Giffen, Quan-Hong Wang, Chaoyu Wang, Stephen M Hewitt, Philip R Taylor |
Journal | Anticancer research
(Anticancer Res)
Vol. 31
Issue 3
Pg. 945-52
(Mar 2011)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 21498718
(Publication Type: Journal Article)
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Chemical References |
- Biomarkers, Tumor
- Carrier Proteins
- Keratin-4
- Microfilament Proteins
- fascin
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Topics |
- Biomarkers, Tumor
(genetics, metabolism)
- Biopsy
- Carcinoma, Squamous Cell
(genetics, metabolism, pathology)
- Carrier Proteins
(genetics, metabolism)
- Esophageal Neoplasms
(genetics, metabolism, pathology)
- Female
- Genes, Neoplasm
(genetics)
- Humans
- Immunohistochemistry
- Keratin-4
(genetics, metabolism)
- Male
- Microfilament Proteins
(genetics, metabolism)
- Middle Aged
- Odds Ratio
- Regression Analysis
- Risk Factors
- Statistics, Nonparametric
- Survival Analysis
- Tissue Array Analysis
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