TY - JOUR
T1 - GLUT 1 receptor expression and circulating levels of fasting glucose in high grade serous ovarian cancer.
AU - Pizzuti, Laura
AU - Sergi, Domenico
AU - Mandoj, Chiara
AU - Antoniani, Barbara
AU - Sperati, Francesca
AU - Chirico, Andrea
AU - Di Lauro, Luigi
AU - Valle, Mario
AU - Garofalo, Alfredo
AU - Vizza, Enrico
AU - Corrado, Giacomo
AU - Tomao, Federica
AU - Rinaldi, Massimo
AU - Carpano, Silvia
AU - Maugeri-Saccà, Marcello
AU - Conti, Laura
AU - Digiesi, Giovanna
AU - Marchetti, Paolo
AU - De Maria Marchiano, Ruggero
AU - Giordano, Antonio
AU - Giordano, Alessandro
AU - Barba, Maddalena
AU - Carosi, Maria A.
AU - Vici, Patrizia
PY - 2018
Y1 - 2018
N2 - In recent years, the poorly remarkable goals achieved in terms of patients' important outcomes for ovarian cancer have fueled our interest toward the study of its metabolic roots. Within this research pipeline, we assessed the association between the expression of the glucose transporter GLUT1, as expressed at the tumor tissue level, and circulating pre-surgical levels of fasting glucose in a case series including data from 40 patients with high FIGO stage serous ovarian cancer. Patients who provided data to the current analysis were randomly selected from a larger cohort. To our purposes, the procedures related to serum and tissue collection, storage and biomarker assessment were highly standardized and centralized at the institutional laboratories. The GLUT1 antibody SPM498 SPRING (REF. E13810) was used at a 1:500 dilution in 2 µm slides. Staining for GLUT1 was observed at the cell membrane level in all the cases assessed, but strong staining was described in 29 (72.5%) of them. The agreement between the two independent reviewers was 100%. Strong GLUT1 staining was inversely associated with circulating levels of fasting glucose, with a particularly striking difference for patients in the lowest fasting glucose tertile (p = 0.044). These results support the biological plausibility of the association of interest. If confirmed in larger studies, our findings may help clarify the potentials of biomarkers related to energy metabolism in terms of prognosis definition, treatment assignment, and outcome interpretation for patients with high FIGO stage serous ovarian cancer.
AB - In recent years, the poorly remarkable goals achieved in terms of patients' important outcomes for ovarian cancer have fueled our interest toward the study of its metabolic roots. Within this research pipeline, we assessed the association between the expression of the glucose transporter GLUT1, as expressed at the tumor tissue level, and circulating pre-surgical levels of fasting glucose in a case series including data from 40 patients with high FIGO stage serous ovarian cancer. Patients who provided data to the current analysis were randomly selected from a larger cohort. To our purposes, the procedures related to serum and tissue collection, storage and biomarker assessment were highly standardized and centralized at the institutional laboratories. The GLUT1 antibody SPM498 SPRING (REF. E13810) was used at a 1:500 dilution in 2 µm slides. Staining for GLUT1 was observed at the cell membrane level in all the cases assessed, but strong staining was described in 29 (72.5%) of them. The agreement between the two independent reviewers was 100%. Strong GLUT1 staining was inversely associated with circulating levels of fasting glucose, with a particularly striking difference for patients in the lowest fasting glucose tertile (p = 0.044). These results support the biological plausibility of the association of interest. If confirmed in larger studies, our findings may help clarify the potentials of biomarkers related to energy metabolism in terms of prognosis definition, treatment assignment, and outcome interpretation for patients with high FIGO stage serous ovarian cancer.
KW - glut-1
KW - glut-1
UR - http://hdl.handle.net/10807/114764
U2 - 10.1002/jcp.26023
DO - 10.1002/jcp.26023
M3 - Article
SN - 0021-9541
SP - 1396
EP - 1401
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
ER -