IMDEA-Food Institute, CEI UAM+CSIC, Madrid, Spain.
Translational Oncology Laboratory, La Paz University Hospital (IdiPAZ), Madrid, Spain; Medical Oncology, Infanta Sofía University Hospital, Madrid, Spain.
Mol Oncol. 2014 Dec;8(8):1469-81. doi: 10.1016/j.molonc.2014.05.015. Epub 2014 Jun 10.
Studies have recently suggested that metabolic syndrome and its components increase the risk of colorectal cancer. Both diseases are increasing in most countries, and the genetic association between them has not been fully elucidated. The objective of this study was to assess the association between genetic risk factors of metabolic syndrome or related conditions (obesity, hyperlipidaemia, diabetes mellitus type 2) and clinical outcome in stage II colorectal cancer patients. Expression levels of several genes related to metabolic syndrome and associated alterations were analysed by real-time qPCR in two equivalent but independent sets of stage II colorectal cancer patients. Using logistic regression models and cross-validation analysis with all tumour samples, we developed a metabolic syndrome-related gene expression profile to predict clinical outcome in stage II colorectal cancer patients. The results showed that a gene expression profile constituted by genes previously related to metabolic syndrome was significantly associated with clinical outcome of stage II colorectal cancer patients. This metabolic profile was able to identify patients with a low risk and high risk of relapse. Its predictive value was validated using an independent set of stage II colorectal cancer patients. The identification of a set of genes related to metabolic syndrome that predict survival in intermediate-stage colorectal cancer patients allows delineation of a high-risk group that may benefit from adjuvant therapy and avoid the toxic and unnecessary chemotherapy in patients classified as low risk. Our results also confirm the linkage between metabolic disorder and colorectal cancer and suggest the potential for cancer prevention and/or treatment by targeting these genes.
最近的研究表明,代谢综合征及其组成部分会增加结直肠癌的风险。这两种疾病在大多数国家都呈上升趋势,它们之间的遗传关联尚未完全阐明。本研究旨在评估代谢综合征或相关疾病(肥胖、高脂血症、2 型糖尿病)的遗传风险因素与 II 期结直肠癌患者临床结局之间的关联。通过实时 qPCR 在两组等效但独立的 II 期结直肠癌患者中分析了与代谢综合征和相关改变相关的几个基因的表达水平。使用逻辑回归模型和所有肿瘤样本的交叉验证分析,我们开发了一个与代谢综合征相关的基因表达谱,以预测 II 期结直肠癌患者的临床结局。结果表明,由先前与代谢综合征相关的基因组成的基因表达谱与 II 期结直肠癌患者的临床结局显著相关。该代谢谱能够识别复发风险低和高的患者。使用另一组独立的 II 期结直肠癌患者验证了其预测价值。鉴定出一组与代谢综合征相关的基因,这些基因可预测中期结直肠癌患者的生存情况,可明确高危组,这些高危组可能受益于辅助治疗,并避免将低危患者分类为化疗带来的毒性和不必要的化疗。我们的结果还证实了代谢紊乱与结直肠癌之间的联系,并表明通过针对这些基因进行癌症预防和/或治疗具有潜力。