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Reduced Claudin-12 Expression Predicts Poor Prognosis in Cervical Cancer
Authors:Abidur Rahman  Makoto Kobayashi  Kotaro Sugimoto  Yuta Endo  Manabu Kojima  Shigenori Furukawa  Takafumi Watanabe  Shu Soeda  Yuko Hashimoto  Keiya Fujimori  Hideki Chiba
Affiliation:1.Department of Basic Pathology, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan; (A.R.); (M.K.); (Y.E.);2.Department of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan; (M.K.); (S.F.); (T.W.); (S.S.); (K.F.);3.Department of Diagnostic Pathology, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan;
Abstract:Background: Within the claudin (CLDN) family, CLDN12 mRNA expression is altered in various types of cancer, but its clinicopathological relevance has yet to be established due to the absence of specific antibodies (Abs) with broad applications. Methods: We generated a monoclonal Ab (mAb) against human/mouse CLDN12 and verified its specificity. By performing immunohistochemical staining and semiquantification, we evaluated the relationship between CLDN12 expression and clinicopathological parameters in tissues from 138 cases of cervical cancer. Results: Western blot and immunohistochemical analyses revealed that the established mAb selectively recognized the CLDN12 protein. Twenty six of the 138 cases (18.8%) showed low CLDN12 expression, and the disease-specific survival (DSS) and recurrence-free survival rates were significantly decreased compared with those in the high CLDN12 expression group. We also demonstrated, via univariable and multivariable analyses, that the low CLDN12 expression represents a significant prognostic factor for the DSS of cervical cancer patients (HR 3.412, p = 0.002 and HR 2.615, p = 0.029, respectively). Conclusions: It can be concluded that a reduced CLDN12 expression predicts a poor outcome for cervical cancer. The novel anti-CLDN12 mAb could be a valuable tool to evaluate the biological relevance of the CLDN12 expression in diverse cancer types and other diseases.
Keywords:claudin  CLDN12  gynecological cancer  tight junction  biomarker  squamous cell carcinoma  adenocarcinoma
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