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Determining the Immunohistochemical Expression of GLUT1 in Renal Cell Carcinoma Using the HSCORE Method

Overview
Journal Biomed Rep
Specialty Biochemistry
Date 2021 Aug 25
PMID 34429965
Citations 4
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Abstract

The aim of the present study was to compare the immunohistochemical expression of glucose transporter 1 (GLUT1) between the most common histological types of renal cell carcinoma (RCC), and to determine whether a correlation between GLUT1 expression and nuclear grade or tumor size exists. A total of 19 RCC samples were selected for the study, consisting of 8 clear cell (cc)RCC and 11 non-ccRCC tissues. Immunohistochemistry for GLUT1 was performed on formalin-fixed and paraffin-embedded sections using GLUT1 antibodies. All data analyses were performed using the MedCalc software. There was a higher immunohistochemical expression of GLUT1 in the ccRCC group compared with the non-cc group, but there was no difference in GLUT1 expression between groups of RCCs with differing nuclear grades. No significant correlation between GLUT1 expression and tumor size was found. The higher immunohistochemical expression of GLUT1 in ccRCC may be a contributing factor to the clinical characteristics and behavior of that group of carcinomas. These results suggest that GLUT1 expression cannot be used as a prognostic factor for RCC, but it may be used as a predictive factor in the future.

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References
1.
Grahame Hardie D, Ashford M . AMPK: regulating energy balance at the cellular and whole body levels. Physiology (Bethesda). 2014; 29(2):99-107. PMC: 3949207. DOI: 10.1152/physiol.00050.2013. View

2.
Kurokawa T, Yoshida Y, Kawahara K, Tsuchida T, Okazawa H, Fujibayashi Y . Expression of GLUT-1 glucose transfer, cellular proliferation activity and grade of tumor correlate with [F-18]-fluorodeoxyglucose uptake by positron emission tomography in epithelial tumors of the ovary. Int J Cancer. 2004; 109(6):926-32. DOI: 10.1002/ijc.20057. View

3.
Padala S, Barsouk A, Thandra K, Saginala K, Mohammed A, Vakiti A . Epidemiology of Renal Cell Carcinoma. World J Oncol. 2020; 11(3):79-87. PMC: 7239575. DOI: 10.14740/wjon1279. View

4.
Page T, Hodgkinson A, Ollerenshaw M, Hammonds J, Demaine A . Glucose transporter polymorphisms are associated with clear-cell renal carcinoma. Cancer Genet Cytogenet. 2005; 163(2):151-5. DOI: 10.1016/j.cancergencyto.2005.07.004. View

5.
Melstrom L, Salabat M, Ding X, Milam B, Strouch M, Pelling J . Apigenin inhibits the GLUT-1 glucose transporter and the phosphoinositide 3-kinase/Akt pathway in human pancreatic cancer cells. Pancreas. 2008; 37(4):426-31. DOI: 10.1097/MPA.0b013e3181735ccb. View