Schroecksnadel Katharina, Frick Barbara, Fiegl Michael, Winkler Christiana, Denz Hubert A, Fuchs Dietmar
Division of Biological Chemistry, Biocentre, Innsbruck Medical University, Innsbruck, Austria.
Clin Chem Lab Med. 2007;45(1):47-53. doi: 10.1515/CCLM.2007.012.
Recently, homocysteine production was observed in tumour cell lines and homocysteine was proposed as a tumour marker. Furthermore, homocysteine production by activated immunocompetent cells was demonstrated.
In this study, homocysteine metabolism and immune activation status were investigated in 128 patients suffering from various types of cancer (haematological disorders, lung cancer, gastrointestinal tumours, gynaecological cancer and tumours of other localisation) and healthy age-matched controls.
A high percentage of patients (39.1%) showed moderate hyperhomocysteinaemia, while cysteine, folate and vitamin B(12) concentrations were within reference ranges. Most patients were found to have elevated concentrations of the immune activation and inflammation markers neopterin and C-reactive protein (CRP), as well as a higher erythrocyte sedimentation rate (ESR). Patients of different cancer groups differed significantly regarding vitamin B(12) and neopterin concentrations; higher B(12) levels were also associated with tumour progression. Univariate regression analysis showed that CRP, ESR and neopterin were suited best to predict death. In multivariate analysis, neopterin was best suited to predicting death, while homocysteine and B vitamins were not associated with patient outcome. Homocysteine concentrations were correlated with folate and cysteine levels. Higher neopterin concentrations coincided with lower folate concentrations, but higher vitamin B(12) concentrations.
Associations between neopterin and folate concentrations may indicate that cellular immune activation might partly contribute to the development of folate deficiency in cancer patients, thus possibly also impairing homocysteine remethylation.
最近,在肿瘤细胞系中观察到同型半胱氨酸的产生,并且同型半胱氨酸被提议作为一种肿瘤标志物。此外,还证实了活化的免疫活性细胞可产生同型半胱氨酸。
在本研究中,对128例患有各种类型癌症(血液系统疾病、肺癌、胃肠道肿瘤、妇科癌症及其他部位肿瘤)的患者以及年龄匹配的健康对照者进行了同型半胱氨酸代谢和免疫激活状态的调查。
高比例的患者(39.1%)表现为中度高同型半胱氨酸血症,而半胱氨酸、叶酸和维生素B12浓度在参考范围内。大多数患者的免疫激活和炎症标志物新蝶呤和C反应蛋白(CRP)浓度升高,同时红细胞沉降率(ESR)也较高。不同癌症组的患者在维生素B12和新蝶呤浓度方面存在显著差异;较高的B12水平也与肿瘤进展相关。单因素回归分析表明,CRP、ESR和新蝶呤最适合预测死亡。多因素分析中,新蝶呤最适合预测死亡,而同型半胱氨酸和B族维生素与患者预后无关。同型半胱氨酸浓度与叶酸和半胱氨酸水平相关。较高的新蝶呤浓度与较低的叶酸浓度一致,但与较高的维生素B12浓度一致。
新蝶呤和叶酸浓度之间的关联可能表明,细胞免疫激活可能部分导致癌症患者叶酸缺乏的发生,从而也可能损害同型半胱氨酸的再甲基化。