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      Expression of the Receptor for Hyaluronic Acid Mediated Motility (RHAMM) in Endometrial Cancer is Associated with Adverse Histologic Parameters and Tumor Progression

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          Abstract

          Endometrial cancer is one of the most common gynecologic malignancies worldwide. Only two agents have been approved by Food and Drug Administration for endometrial cancer since 1971. There is a need to identify molecular targets to treat advanced endometrial cancer. The receptor for hyaluronan-mediated motility (RHAMM) is upregulated in various types of cancer. Here, we aimed to determine the clinical significance of RHAMM expression in endometrial cancer. Two hundred and twenty-five cases of endometrial cancer, including serous and endometrioid types, and 8 cases of normal endometrium were used for studying RHAMM protein levels. Publically available The Cancer Genome Atlas (TCGA) database was also queried for RHAMM mRNA expression in endometrial cancer. Increased expression of RHAMM protein was seen in endometrial cancer compared with no or weak expression in normal endometrium. RHAMM expression positively correlated with tumor grade. RHAMM expression was significantly increased in endometrial serous carcinomas, which are high-grade, aggressive types of endometrial cancer, compared with the relatively less aggressive endometrioid carcinomas. RHAMM expression also correlated with the presence of lymphovascular invasion. RHAMM mRNA expression correlated with decreased survival in the TCGA cohort. Therefore, increased RHAMM expression in endometrial cancer is associated with high-grade tumors and is indicative of more aggressive behavior. These findings suggest RHAMM as a prognostic factor in endometrial cancer and as a potential therapeutic target in advanced endometrial cancer for future studies.

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          Author and article information

          Journal
          100888796
          21780
          Appl Immunohistochem Mol Morphol
          Appl Immunohistochem Mol Morphol
          Applied immunohistochemistry & molecular morphology : AIMM
          1541-2016
          1533-4058
          6 October 2020
          July 2020
          09 October 2020
          : 28
          : 6
          : 453-459
          Affiliations
          [1 ]Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10065
          [2 ]Division of Biostatistics and Epidemiology, Department of Healthcare Policy and Research, Weill Cornell Medicine, New York, NY 10065
          [3 ]Laboratory of Cellular Oncology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892
          Author notes
          [* ]Corresponding author: Yi-Chieh Nancy Du, Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10065. Phone: 212-746-7312; Fax: 212-746-4483; nad2012@ 123456med.cornell.edu
          Article
          PMC7546253 PMC7546253 7546253 nihpa1634572
          10.1097/PAI.0000000000000763
          7546253
          30920393
          0615e908-7359-4bf9-8509-d11d83ce030a
          History
          Categories
          Article

          prognosis,RHAMM,tumor progression,serous,endometrial cancer
          prognosis, RHAMM, tumor progression, serous, endometrial cancer

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