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Original Paper

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Pathobiological Implications of MUC16/CA125 Expression in Intrahepatic Cholangiocarcinoma-Mass Forming Type

Higashi M.a · Yamada N.a · Yokoyama S.a · Kitamoto S.a · Tabata K.a · Koriyama C.b · Batra S.c · Yonezawa S.a

Author affiliations

Departments of aHuman Pathology, Field of Oncology, and bEpidemiology and Preventive Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan; cDepartments of Biochemistry and Molecular Biology, Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebr., USA

Corresponding Author

Michiyo Higashi, MD, PhD

Department of Human Pathology, Field of Oncology

Kagoshima University Graduate School of Medical and Dental Sciences

8-35-1 Sakuragaoka, Kagoshima 890-8544 (Japan)

Tel. +81 99 275 5270, E-Mail east@m2.kufm.kagoshima-u.ac.jp

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Pathobiology 2012;79:101–106

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Abstract

Objectives: MUC16 carries the peptide epitope CA125, which is well known as a marker of ovarian cancer. High serum levels of MUC16 (CA125) have been reported not only in patients with ovarian cancer but also in patients with liver diseases. We evaluated the expression of MUC16 in intrahepatic cholangiocarcinoma-mass forming type (ICC-MF) tissues. Methods: We examined the expression of MUC16 by immunohistochemical analyses using the monoclonal antibody M11 in ICC-MF tissues from 63 patients. To compare the prevalence of each mucin expression by clinicopathological features, appropriate statistical analysis was performed. Results: MUC16 was detected in 48% of samples (30/63). After adjusting for the effects of other prognostic factors, multivariate survival analysis revealed that MUC16 expression is a significant independent factor of poor prognosis (p = 0.005). Conclusion: The current results indicate that MUC16 expression is a prognostic factor of poor survival in ICC-MF.

© 2012 S. Karger AG, Basel


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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: September 12, 2011
Accepted: November 11, 2011
Published online: January 27, 2012
Issue release date: February 2012

Number of Print Pages: 6
Number of Figures: 2
Number of Tables: 3

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

For additional information: https://www.karger.com/PAT


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