Epithelial mesenchymal transition and cancer stem cells in esophageal adenocarcinoma originating from barrett's esophagus

Yutaka Tomizawa, Tsung Teh Wu, Kenneth Ke Ning Wang

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Carcinomas comprise cohesive epithelial cells linked to one another by E-cadherin-based cell-cell junctions. Epithelial mesenchymal transition (EMT) enables carcinoma cells to migrate from the original tissue and invade into stromal components. The E-cadherin promoter is frequently repressed by specific transcriptional repressors including Snail, Slug and Twist. CD133 is known to be a marker of tumor-initiating cells in human cancers. This is the first study to characterize the transcriptional factors for E-cadherin and the representative cancer stem cell marker in specimens of early esophageal adenocarcinoma (EAC) originating from Barrett's esophagus. Ten surgically treated patients were analyzed in the present study. Immunohistochemistry was performed to determine the expression of Snail, Slug, Twist and CD133, and the results were scored. Unlike previous studies of advanced stage esophageal cancers showing the overexpression of each specific transcriptional protein, the invading edges of the tumor were found to abundantly express Snail, Slug, Twist and CD133 in our cohort. Therefore, results of this study suggest that early stage cancers predominantly comprise cells with metastatic potential and this evidence adds legitimacy to the complete removal of early EAC.

Original languageEnglish (US)
Pages (from-to)1059-1063
Number of pages5
JournalOncology Letters
Volume3
Issue number5
DOIs
StatePublished - May 2012

Fingerprint

Gastropoda
Epithelial-Mesenchymal Transition
Barrett Esophagus
Neoplastic Stem Cells
Cadherins
Mesenchymal Stromal Cells
Adenocarcinoma
Carcinoma
Illegitimacy
Neoplasms
Intercellular Junctions
Esophageal Neoplasms
Epithelial Cells
Immunohistochemistry
Proteins

Keywords

  • Barrett's esophagus
  • Cancer stem cell
  • Epithelial mesenchymal transition
  • Esophageal adenocarcinoma

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Epithelial mesenchymal transition and cancer stem cells in esophageal adenocarcinoma originating from barrett's esophagus. / Tomizawa, Yutaka; Wu, Tsung Teh; Wang, Kenneth Ke Ning.

In: Oncology Letters, Vol. 3, No. 5, 05.2012, p. 1059-1063.

Research output: Contribution to journalArticle

@article{d3012f466bac44a48bf4c4a0145ec536,
title = "Epithelial mesenchymal transition and cancer stem cells in esophageal adenocarcinoma originating from barrett's esophagus",
abstract = "Carcinomas comprise cohesive epithelial cells linked to one another by E-cadherin-based cell-cell junctions. Epithelial mesenchymal transition (EMT) enables carcinoma cells to migrate from the original tissue and invade into stromal components. The E-cadherin promoter is frequently repressed by specific transcriptional repressors including Snail, Slug and Twist. CD133 is known to be a marker of tumor-initiating cells in human cancers. This is the first study to characterize the transcriptional factors for E-cadherin and the representative cancer stem cell marker in specimens of early esophageal adenocarcinoma (EAC) originating from Barrett's esophagus. Ten surgically treated patients were analyzed in the present study. Immunohistochemistry was performed to determine the expression of Snail, Slug, Twist and CD133, and the results were scored. Unlike previous studies of advanced stage esophageal cancers showing the overexpression of each specific transcriptional protein, the invading edges of the tumor were found to abundantly express Snail, Slug, Twist and CD133 in our cohort. Therefore, results of this study suggest that early stage cancers predominantly comprise cells with metastatic potential and this evidence adds legitimacy to the complete removal of early EAC.",
keywords = "Barrett's esophagus, Cancer stem cell, Epithelial mesenchymal transition, Esophageal adenocarcinoma",
author = "Yutaka Tomizawa and Wu, {Tsung Teh} and Wang, {Kenneth Ke Ning}",
year = "2012",
month = "5",
doi = "10.3892/ol.2012.632",
language = "English (US)",
volume = "3",
pages = "1059--1063",
journal = "Oncology Letters",
issn = "1792-1074",
publisher = "Spandidos Publications",
number = "5",

}

TY - JOUR

T1 - Epithelial mesenchymal transition and cancer stem cells in esophageal adenocarcinoma originating from barrett's esophagus

AU - Tomizawa, Yutaka

AU - Wu, Tsung Teh

AU - Wang, Kenneth Ke Ning

PY - 2012/5

Y1 - 2012/5

N2 - Carcinomas comprise cohesive epithelial cells linked to one another by E-cadherin-based cell-cell junctions. Epithelial mesenchymal transition (EMT) enables carcinoma cells to migrate from the original tissue and invade into stromal components. The E-cadherin promoter is frequently repressed by specific transcriptional repressors including Snail, Slug and Twist. CD133 is known to be a marker of tumor-initiating cells in human cancers. This is the first study to characterize the transcriptional factors for E-cadherin and the representative cancer stem cell marker in specimens of early esophageal adenocarcinoma (EAC) originating from Barrett's esophagus. Ten surgically treated patients were analyzed in the present study. Immunohistochemistry was performed to determine the expression of Snail, Slug, Twist and CD133, and the results were scored. Unlike previous studies of advanced stage esophageal cancers showing the overexpression of each specific transcriptional protein, the invading edges of the tumor were found to abundantly express Snail, Slug, Twist and CD133 in our cohort. Therefore, results of this study suggest that early stage cancers predominantly comprise cells with metastatic potential and this evidence adds legitimacy to the complete removal of early EAC.

AB - Carcinomas comprise cohesive epithelial cells linked to one another by E-cadherin-based cell-cell junctions. Epithelial mesenchymal transition (EMT) enables carcinoma cells to migrate from the original tissue and invade into stromal components. The E-cadherin promoter is frequently repressed by specific transcriptional repressors including Snail, Slug and Twist. CD133 is known to be a marker of tumor-initiating cells in human cancers. This is the first study to characterize the transcriptional factors for E-cadherin and the representative cancer stem cell marker in specimens of early esophageal adenocarcinoma (EAC) originating from Barrett's esophagus. Ten surgically treated patients were analyzed in the present study. Immunohistochemistry was performed to determine the expression of Snail, Slug, Twist and CD133, and the results were scored. Unlike previous studies of advanced stage esophageal cancers showing the overexpression of each specific transcriptional protein, the invading edges of the tumor were found to abundantly express Snail, Slug, Twist and CD133 in our cohort. Therefore, results of this study suggest that early stage cancers predominantly comprise cells with metastatic potential and this evidence adds legitimacy to the complete removal of early EAC.

KW - Barrett's esophagus

KW - Cancer stem cell

KW - Epithelial mesenchymal transition

KW - Esophageal adenocarcinoma

UR - http://www.scopus.com/inward/record.url?scp=84863297392&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84863297392&partnerID=8YFLogxK

U2 - 10.3892/ol.2012.632

DO - 10.3892/ol.2012.632

M3 - Article

AN - SCOPUS:84863297392

VL - 3

SP - 1059

EP - 1063

JO - Oncology Letters

JF - Oncology Letters

SN - 1792-1074

IS - 5

ER -