Research Papers:
Role of glucose metabolism related gene GLUT1 in the occurrence and prognosis of colorectal cancer
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Abstract
Wenming Feng1, Ge Cui2, Cheng-Wu Tang1, Xiao-Lan Zhang2, Chuang Dai3, Yong-Qiang Xu3, Hui Gong4, Tao Xue4, Hui-Hui Guo4 and Ying Bao3
1Department of Hepatobiliary Pancreatic Surgery, The First Affiliated Hospital of Huzhou University, Huzhou, Zhejiang Province, P.R. China
2Department of Pathology, The First Affiliated Hospital of Huzhou University, Huzhou, Zhejiang Province, P.R. China
3Department of Surgery, The First Affiliated Hospital of Huzhou University, Huzhou, Zhejiang Province, P.R. China
4Central Laboratory, The First Affiliated Hospital of Huzhou University, Huzhou, Zhejiang Province, P.R. China
Correspondence to:
Ying Bao, email: [email protected]
Keywords: colorectal cancer, GLUT1, polymorphism, prognosis
Received: March 24, 2017 Accepted: April 21, 2017 Published: May 23, 2017
ABSTRACT
Colorectal cancer (CRC) ranks the third most commonly diagnosed cancer in males and the second in females worldwide. However, the functional and causal SNPs for CRC remain to be mined. Glucose transporter 1 (GLUT1), a pivotal rate-limiting element in the transport of glucose in malignancy cells, has been identified to be associated with many cancers. Here, we aim to explore the role of GLUT1 in the occurrence and prognosis of colorectal cancer in a Chinese population. We found that GLUT1 expression levels in CRC tumor tissues were significantly higher than those in the corresponding adjacent normal tissues, and Cox multivariate analysis demonstrated that the GLUT1 expression was an independent prognostic factor for CRC (HR = 2.11, 95% CI = 1.33–3.34, P=0.001). For a functional polymorphism of GLUT1 (rs710218), we found that individuals with TT genotype (OR = 1.68, 95% CI = 1.02-2.75, P = 0.041) or AT genotype (OR = 1.47, 95% CI = 1.09-1.99, P = 0.012) of rs710218 had a significantly increased risk of CRC compared to those with AA homozygote. These findings strongly suggest that glucose metabolism related gene GLUT1, and its functional SNP, rs710218 might contribute to CRC susceptibility and prognosis, and the exact biological mechanism awaits further research.
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