Prognostic impact of the combination of glucose transporter 1 and ATP citrate lyase in node-negative patients with non-small lung cancer

过剩1 医学 ATP柠檬酸裂解酶 葡萄糖转运蛋白 癌症研究 肿瘤科 脂肪生成 内科学 比例危险模型 生存分析 生物 生物化学 新陈代谢 柠檬酸合酶 胰岛素
作者
Jun Osugi,Takumi Yamaura,Satoshi Muto,Naoyuki Okabe,Yuki Matsumura,Mika Hoshino,Mitunori Higuchi,Hiroyuki Suzuki,Mitsukazu Gotoh
出处
期刊:Lung Cancer [Elsevier BV]
卷期号:88 (3): 310-318 被引量:55
标识
DOI:10.1016/j.lungcan.2015.03.004
摘要

Objective Metabolic alternations are deemed a hallmark of cancer cells. Among many metabolic pathways, glycolysis and lipogenesis are essential metabolic processes in cancer cells. In this study, we examined the prognostic impact of the combined expression of glycolysis-related glucose transporter 1 (GLUT1) and ATP-citrate lyase (ACLY), which are important molecules in lipogenesis, in patients with non-small cell lung cancer (NSCLC). Materials and methods GLUT1 and ACLY expression in 134 NSCLC specimens were determined by immunohistochemistry using a tissue microarray (TMA). We examined the overall survival of patients with GLUT1-, ACLY- or GLUT + ACLY-positive expression using Kaplan–Meier analysis. We analyzed the prognostic impact of combined GLUT1 and ACLY expression according to lymph node status using multivariate Cox analysis. Results Patients with GLUT1- or ACLY-positive expression exhibited poorer overall survival compared with GLUT1- or ACLY-negative patients. GLUT1-positive/ACLY-positive expression status was associated with the worst overall survival, in contrast with GLUT1 negative/ACLY-negative expression status, which was correlated with the best overall survival (P = 0.003). GLUT1-positive/ACLY-positive expression was significantly correlated with poor prognosis in node-negative but not in node-positive patients. Multivariate Cox analysis indicated combined expression of GLUT1 and ACLY was an independent prognostic factor for overall survival in node-negative patients with NSCLC (P = 0.049). Conclusion These results suggest that the combined expression of GLUT1 and ACLY could be a more valuable prognostic factor than their individual expression in node-negative patients with NSCLC.
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