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Original Paper

EphB1 Is Underexpressed in Poorly Differentiated Colorectal Cancers

Sheng Z.a · Wang J.a, b · Dong Y.a · Ma H.a · Zhou H.a · Sugimura H.c · Lu G.b · Zhou X.a

Author affiliations

aDepartment of Pathology, Clinical School of Medical College of Nanjing University/Nanjing Jinling Hospital, and bCenter for Molecular Imaging Research, Department of Radiology, Nanjing Jinling Hospital, Nanjing, PR China; cDepartment of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan

Corresponding Author

Xiaojun Zhou, MD, PhD

Department of Pathology

Nanjing University School of Medicine/Nanjing Jinling Hospital

Nanjing 210002 (PR China)

Tel. +86 25 8086 1292, Fax +86 25 8086 0191, E-Mail nanjing_81@yahoo.com

Related Articles for ""

Pathobiology 2008;75:274–280

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Background: Over- or underexpression of certain Eph receptors has been associated with tumorigenesis of some types of cancer. EphB1 is a member of receptor tyrosine kinases of the EphB subfamily involved in the development, progress and prognosis of colorectal cancers. The expression levels of EphB1 in colon cancer cell lines and human colorectal carcinoma specimens were determined and association of EphB1 expression with clinicopathological parameters was analyzed. Methods: Quantitative real-time reverse transcription polymerase chain reaction and immunohistochemistry were used. Results: The EphB1 transcript is expressed in all colon cancer cell lines tested. However, there is marked variability in the expression of the EphB1 transcripts and proteins among colorectal carcinoma specimens. Reduced expression of EphB1 in colorectal cancers more often occurred in poorly differentiated and mucinous adenocarcinomas than in well- and moderately differentiated adenocarcinomas. Further, cancer cells with a low level of EphB1 protein showed more invasive power. Conclusion: Our data indicate that EphB1 may have roles in the pathogenesis and development of colorectal cancer.

© 2008 S. Karger AG, Basel

Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: September 19, 2007
Accepted: February 18, 2008
Published online: October 15, 2008
Issue release date: October 2008

Number of Print Pages: 7
Number of Figures: 3
Number of Tables: 3

ISSN: 1015-2008 (Print)
eISSN: 1423-0291 (Online)

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