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Updated: Jun 2, 2026

Assessment of Ovarian Cancer Spheroid Attachment and Invasion of Mesothelial Cells in Real Time
Published on: May 20, 2014
Claudin 4 Is differentially expressed between ovarian cancer subtypes and plays a role in spheroid formation
Kristin L M Boylan1, Benjamin Misemer, Melissa S De Rycke
1Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA; E-Mails: boyla002@umn.edu (K.L.M.B.); benjamin.misemer@gmail.com (B.M.); deryc004@umn.edu (M.S.D.); ande0555@umn.edu (J.D.A.); harr0750@umn.edu (K.M.H.); pambu001@umn.edu (S.E.P.).
Abstract:
Claudin 4 is a cellular adhesion molecule that is frequently overexpressed in ovarian cancer and other epithelial cancers. In this study, we sought to determine whether the expression of claudin 4 is associated with outcome in ovarian cancer patients and may be involved in tumor progression. We examined claudin 4 expression in ovarian cancer tissues and cell lines, as well as by immunohistochemical staining of tissue microarrays (TMAs; n = 500), spheroids present in patients' ascites, and spheroids formed in vitro. Claudin 4 was expressed in nearly 70% of the ovarian cancer tissues examined and was differentially expressed across ovarian cancer subtypes, with the lowest expression in clear cell subtype. No association was found between claudin 4 expression and disease-specific survival in any subtype. Claudin 4 expression was also observed in multicellular spheroids obtained from patients' ascites. Using an in vitro spheroid formation assay, we found that NIH:OVCAR5 cells treated with shRNA against claudin 4 required a longer time to form compact spheroids compared to control NIH:OVCAR5 cells that expressed high levels of claudin 4. The inability of the NIH:OVCAR5 cells treated with claudin 4 shRNA to form compact spheroids was verified by FITC-dextran exclusion. These results demonstrate a role for claudin 4 and tight junctions in spheroid formation and integrity.
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