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Issue 1086 coverIntegrated Molecular Medicine for Neuronal and Neoplastic Disorders Volume 1086 published November 2006
Ann. N.Y. Acad. Sci. 1086: 233–240 (2006). doi: 10.1196/annals.1377.007
Copyright © 2006 by the New York Academy of Sciences
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Part V. Novel Targets for Cancer Therapy

Involvement of DPPIV/CD26 in Epithelial Morphology and Suppressed Invasive Ability in Ovarian Carcinoma Cells

HIROAKI KAJIYAMAa, KIYOSUMI SHIBATAa, MIKIO TERAUCHIa, KAZUHIKO INOa, AKIHIRO NAWAa AND FUMITAKA KIKKAWAa

a Department of Obstetrics and Gynecology, Nagoya University Graduate School of Medicine, Tsurumai-cho 65, Showa-ku, Nagoya 466-8550, Japan

Key Words: DPPIV/CD26 • morphology • invasion • MMP-2 • ovarian carcinoma

Address for correspondence: Hiroaki Kajiyama, Department of Obstetrics and Gynecology, Nagoya Graduate University School of Medicine, Tsurumai-cho 65, Showa-ku, Nagoya 466-8550, Japan. Voice: +81-52-744-2263; fax: +81-52-744-2268.  e-mail: kajiyama{at}med.nagoya-u.ac.jp

Dipeptidyl peptidase IV (DPPIV) is a multifunctional cell surface aminopeptidase with ubiquitous expression and it has a variety of functional properties in the development of human malignancies. In the present study, we showed the possible correlation between DPPIV/CD26 expression and less migratory potential with decreased MMP-2 expression in ovarian carcinoma cells. Moreover, induction of DPPIV/CD26 resulted in reduced expressions of MMP-2 and mesenchymal markers such as vimentin and SMA, with a less invasive potential and an epithelial morphologic change. This evidence implies that DPPIV/CD26 may play a crucial role in the antimetastatic potential in ovarian carcinoma.






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