Abstract

There is a tremendous need for developing new useful prognostic factors in ovarian cancer. Galectins are a family of carbohydrate binding proteins which have been suggested to serve as prognostic factors for various cancer types. In this study, the presence of Galectin-1, -3, and -7 was investigated in 156 ovarian cancer specimens by immunochemical staining. Staining was evaluated in the cytoplasm and nucleus of cancer cells as well as the peritumoral stroma using a semi quantitative score (Remmele (IR) score). Patients’ overall survival was compared between different groups of Galectin expression. Galectin (Gal)-1 and -3 staining was observed in the peritumoral stroma as well as the nucleus and cytoplasm of tumor cells, while Gal-7 was only present in the cytoplasm of tumor cells. Patients with Gal-1 expression in the cytoplasm or high Gal-1 expression in the peritumoral stroma showed reduced overall survival. Nuclear Gal-3 staining correlated with a better outcome. We observed a significantly reduced overall survival for cases with high Gal-7 expression and a better survival for Gal-7 negative cases, when compared to cases with low expression of Gal-7. We were able to show that both tumor and stroma staining of Gal-1 could serve as negative prognostic factors for ovarian cancer. We were able to confirm cytoplasmic Gal-7 as a negative prognostic factor. Gal-3 staining in the nucleus could be a new positive prognosticator for ovarian cancer.

Highlights

  • Ovarian cancer is the most lethal gynecological malignancy, ranking fifth in estimated cancer deaths among women in the USA [1]

  • Galectin-1 staining was successfully performed on 150 ovarian cancer specimens

  • Gal-1 was present in the cytoplasm and the nuclei of ovarian cancer cells, as well as the peritumoral stroma (Figure 1)

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Summary

Introduction

Ovarian cancer is the most lethal gynecological malignancy, ranking fifth in estimated cancer deaths among women in the USA [1]. Extent of residual disease after surgery, histological subtype, and a high volume of ascites can be used as prognosticators in ovarian cancer [4]. Carbohydrate stem cell marker TF1 has been proposed as negative prognostic marker in ovarian cancer displaying wildtype p53, while estrogen receptor promoter methylation could predict overall survival in low-grade ovarian carcinoma patients [5,6]. For these and various other molecules the prognostic value independently of clinical parameters has been proven, until today, except for breast cancer gene (BRCA)-status, no biological marker is commonly accepted [4]. Further specification of anti-cancer therapy necessarily requires an improvement of biological prognostic markers in ovarian cancer

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