Novel predictive biomarkers for cervical cancer prognosis

被引:14
|
作者
Moreno-Acosta, Pablo [1 ]
Carrillo, Schyrly [1 ]
Gamboa, Oscar [2 ]
Romero-Rojas, Alfredo [3 ]
Acosta, Jinneth [4 ]
Molano, Monica [5 ]
Balart-Serra, Joseph [6 ]
Cotes, Martha [7 ]
Rancoule, Chloe [8 ]
Magne, Nicolas [8 ,9 ]
机构
[1] Univ Nacl Colombia, Res Grp Canc Biol, Res Grp Radiobiol Clin Mol & Celular, Bogota, Colombia
[2] Univ Nacl Colombia, Anal Unit, Bogota, Colombia
[3] Univ Nacl Colombia, Natl Canc Inst, Pathol Oncol Grp, Bogota, Colombia
[4] Univ Nacl Colombia, Pathol Grp, Bogota, Colombia
[5] Royal Womens Hosp, Microbiol & Infect Dis, Melbourne, Vic, Australia
[6] SanPau Hosp, Radiat Oncol Dept, Barcelona, Spain
[7] Natl Canc Inst, Dept Radiotherapy, Bogota, Colombia
[8] Lucien Neuwirth Canc Inst, Dept Radiotherapy, 108bis Ave Albert Raimond, F-42270 St Priest En Jarez, France
[9] Fac Med Lyon Sud, Lab Radiobiol, EMR3738, Pierre Benite, France
关键词
cervical cancer; biomarkers; carbonic anhydrase IX; glucose transporter type 1; hexokinase; anemic hypoxia;
D O I
10.3892/mco.2016.1055
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High hypoxic, glycolytic and acidosis metabolisms characterize cervical cancer tumors and have been described to be involved in chemoradioresistance mechanisms. Based on these observations, the present study assessed four selected novel biomarkers on the prognosis of locally advanced cervical carcinoma. A total of 66 patients with stage IIB/IIIB cervical cancer were retrospectively included. The protein expression levels of glucose transporter 1 (GLUT1), carbonic anhydrase 9 (CAIX) and hexokinase 1 (HKII) were investigated by immunohistochemistry on tumor biopsies, hemoglobin was measured and the disease outcome was monitored. A total of 53 patients (80.3%) presented a complete response. For these patients, the protein expression levels of GLUT1, CAIX and HKII were overexpressed. A significant difference was observed (P=0.0127) for hemoglobin levels (<= 11 g/dl) in responsive compared with non-responsive patients. The expression of GLUT1 is associated with a lower rate of both overall and disease-free survival, with a trend of decreased risk of 1.1x and 1.5x, respectively. Co-expression of GLUT1 and HKII is associated with a decreased trend risk of 1.6x for overall survival. Patients with hemoglobin levels <= 11 g/dl had a 4.3-fold risk (P=0.02) in decreasing both to the rate of overall and disease-free survival. The presence of anemic hypoxia (hemoglobin <= 11 g/dl) and the expression of GLUT1 and/or HKII influence treatment response and are associated with a lower overall and disease-free survival. The present results demonstrated that these biomarkers may be used as predictive markers and suggested that these metabolic pathways can be used as potential novel therapeutic targets.
引用
收藏
页码:792 / 796
页数:5
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