Table 2. Association between histology grade, lymph node status,

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Table 2. Association between histology grade, lymph node status, CLAUDIN-7 CORRELATES WITH BREAST CARCINOMA HISTOLOGICAL GRADE BUT NOT WITH OUTCOME E. A. Khramtsova1, V. Macias1, M. K. Patel1, J. Akhtar1, O. Jee3, W. Gao2, W-M. Liang2, C. Beam2, B. Gilks4, E. Wiley1 and A. K. Balla1 1 Department of Pathology, University of Illinois-Chicago, Chicago, IL, USA, 2 Department of Epidemiology and Biostatistics, University of Illinois-Chicago, Chicago, IL, USA, 3 Carleton College, Northfield, MN, USA, 4 Department of Pathology, University of British Columbia, Vancouver, Canada   UIC UIC UNIVERSITY OF ILLINOIS AT CHICAGO UNIVERSITY OF ILLINOIS AT CHICAGO Table 2. Association between histology grade, lymph node status, outcomes and claudin -7 score by using Fisher’s exact test INTRODUCTION Invasive breast carcinoma is the most common malignancy and is the second most common cause of cancer death in the United States among women. Metastasis is the primary cause of fatality in breast cancer patients. Since claudin-7 serves an important role in both epithelial cell tight junction formation and function, several studies have investigated its utility as a biomarker for breast cancer. Normal breast epithelial cells have strong expression of claudin-7. Previous publications have shown an inverse correlation of claudin-7 immunohistochemical expression and breast cancer histological grade. However, no formal study has been performed to investigate whether claudin-7 immunohistochemical expression can be used as prognostic marker. This study aims to determine whether claudin-7 expression correlates with breast cancer outcomes. Variable Claudin-7 Score % P-value 1 2 3 Histology grade 0.27 Grade 1 16.67 9.68 5.45 Grade 2 25.00 31.18 47.27 41.67 Grade 3 58.33 59.14 Node status 0.07 Negative 90.00 68.13 51.92 57.14 Positive 10.00 31.87 48.08 42.86 Disease outcome status 0.74 Death of breast 15.38 31.34 26.67 Death from other reasons 23.08 20.37 22.39 33.33 Alive 61.54 54.63 46.27 40.00 Figure 2. View of the ImageScope viewer (Aperio ScanScope) shows TMA cores with immunohistochemical staining of Claudin-7 MATERIALS AND METHODS Breast tissues for TMA construction were obtained from the Department of Surgical Pathology archive at the Vancouver General Hospital with local ethical committee approval. The samples were de-identified and data used under anonymous numbers. TMA was generated using Tissue Arrayer®. Immunohistochemical staining on TMA slides was performed with rabbit anti-claudin-7 antibody (Zymed). Pathologist-based semiquantitative analysis was determined by evaluating the intensity of the membrane reaction for claudin-7 with the HercepTest criteria. Automated image analysis performed by HercepTest algorithm with TMALab software (Aperio ScanScope). Interpretation of claudin-7 expression (staining intensity criteria) Score: 0 Staining Pattern :No staining is observed or membrane staining is observed in less than 10% of the tumor cells . Score: 1+ Staining Pattern: A faint/barely perceptible membrane staining is detected in more than 10% of the tumor cells. The cells are only stained in part of their membrane. Score: 2+ Staining Pattern: A weak to moderate complete membrane staining is observed in more than 10% of the tumor cells. Score: 3+ Staining Pattern: A strong complete membrane staining is observed in more than 10% of the tumor cells. Table 3. Test association between tumor size and claudin -7 score Variable Mean±STD P-value Claudin-7 Score 1 2 3 Tumor size 3.42±2.78 2.74±1.91 3.35±3.50 2.41±1.04 0.36 RESULTS Table 1. Descriptive statistics for categorical variables ( total sample size=207) CONCLUSIONS There is no statistical correlation between the digital image score analysis of claudin-7 and outcomes and between claudin-7 and any of the other parameters (stage, grade, and positive lymph node). Variable N % Claudin-7 Immunohistochemistry Score 14 6.76 1 110 53.14 2 68 32.85 3 15 7.25 Histology grade (missing=35) Grade 1 16 9.30 Grade 2 63 36.63 Grade 3 93 54.07 Node status (missing=40) Negative 106 63.47 Positive 61 36.53 Disease outcome status (missing=4) Death of breast cancer 54 26.60 Death from other reasons 45 22.17 Alive 104 51.23 Detail of the previous image REFERENCES  Berx G, Van Roy F: The E-cadherin/catenin complex: an important gatekeeper in breast cancer tumorigenesis and malignant progression. Breast Cancer Res (2001) 3:289-293. Itoh M, Furuse M, Morita K, Kubota K, Saitou M and Tsukita S. (1999). J.CellBiol., 147, 1351–1363. Kominsky S, Argani P, Korz S, Evron W, Raman V, Garrett E, Rein A, Sauter G, Kallioniemi O and Sukumar S. Loss of the tight junction protein claudin-7 correlates with histological grade in both ductal carcinoma in situ and invasive ductal carcinoma of the breast. Oncogene (2003) 22:2021-2033 Tokes A, Kulka J, Paku S, Mathe M, Paska C, Lodi C, Kiss A and Schaff Z. The expression of five different claudins in invasive breast carcinomas: Comparison of pT1pN1 and pT1pN0 tumors. Pathology - Research and Practice (2005) 201:537-544. Mullin J. Potential interplay between luminal growth factors and increased tight junction permeability in epithelial carcinogenesis. J Exp. Zool (1997) 279:484-489. Tsukita S, Furuse M. Occludin and claudins in tight-junction strands: leading or supporting players? Trends Cell Biol (1999) 9:268–73. Tissue microarray (TMA) block TMA slides immunostained with anti-claudin-7 Figure 1. Methodology of tissue microarray technology in the evaluation of claudin-7 expression