University of Edinburgh, Clinical and Surgical Sciences (Surgery), Royal Infirmary, Edinburgh, UK.
EMBO Mol Med. 2012 Jun;4(6):462-71. doi: 10.1002/emmm.201200231. Epub 2012 Apr 4.
The variable predisposition to cachexia may, in part, be due to the interaction of host genotype. We analyzed 129 single nucleotide polymorphisms (SNPs) in 80 genes for association with cachexia based on degree of weight loss (>5, >10, >15%) as well as weight loss in the presence of systemic inflammation (C-reactive protein, > 10 mg/l). 775 cancer patients were studied with a validation association study performed on an independently recruited cohort (n = 101) of cancer patients. The C allele (minor allele frequency 10.7%) of the rs6136 (SELP) SNP was found to be associated with weight loss >10% both in the discovery study (odds ratio (OR) 0.52; 95% confidence intervals (CI), 0.29-0.93; p = 0.026) and the validation study (OR 0.09, 95% CI 0.01-0.98, p = 0.035). In separate studies, induction of muscle atrophy gene expression was investigated using qPCR following either tumour-induced cachexia in rats or intra-peritoneal injection of lipopolysaccharide in mice. P-selectin was found to be significantly upregulated in muscle in both models. Identification of P-selectin as relevant in both animal models and in cachectic cancer patients supports this as a risk factor/potential mediator in cachexia.
个体易发生恶病质的这种可变性部分可能与宿主基因型的相互作用有关。我们分析了 80 个基因中的 129 个单核苷酸多态性(SNP),以确定它们与体重减轻(>5%、>10%、>15%)以及存在全身炎症(C 反应蛋白>10mg/L)时的体重减轻的相关性。对 775 名癌症患者进行了研究,并对独立招募的癌症患者队列(n=101)进行了验证关联研究。rs6136(SELP)SNP 的 C 等位基因(小等位基因频率 10.7%)与体重减轻>10%相关,在发现研究(优势比(OR)0.52;95%置信区间(CI)0.29-0.93;p=0.026)和验证研究(OR 0.09,95%CI 0.01-0.98,p=0.035)中均如此。在单独的研究中,我们使用 qPCR 研究了大鼠肿瘤诱导恶病质或小鼠腹腔注射脂多糖后肌肉萎缩基因表达的诱导情况。在这两种模型中,选择素 P 均在肌肉中显著上调。选择素 P 在两种动物模型和恶病质癌症患者中都具有相关性,这支持其作为恶病质的风险因素/潜在介质。