首页> 外文期刊>Genome Medicine >Serum metabolomic profile as a means to distinguish stage of colorectal cancer
【24h】

Serum metabolomic profile as a means to distinguish stage of colorectal cancer

机译:血清代谢组学谱作为区分大肠癌分期的一种手段

获取原文
       

摘要

Background Presently, colorectal cancer (CRC) is staged preoperatively by radiographic tests, and postoperatively by pathological evaluation of available surgical specimens. However, present staging methods do not accurately identify occult metastases. This has a direct effect on clinical management. Early identification of metastases isolated to the liver may enable surgical resection, whereas more disseminated disease may be best treated with palliative chemotherapy. Methods Sera from 103 patients with colorectal adenocarcinoma treated at the same tertiary cancer center were analyzed by proton nuclear magnetic resonance (1H NMR) spectroscopy and gas chromatography-mass spectroscopy (GC-MS). Metabolic profiling was done using both supervised pattern recognition and orthogonal partial least squares-discriminant analysis (O-PLS-DA) of the most significant metabolites, which enables comparison of the whole sample spectrum between groups. The metabolomic profiles generated from each platform were compared between the following groups: locoregional CRC (N = 42); liver-only metastases (N = 45); and extrahepatic metastases (N = 25). Results The serum metabolomic profile associated with locoregional CRC was distinct from that associated with liver-only metastases, based on 1H NMR spectroscopy ( P = 5.10 × 10-7) and GC-MS ( P = 1.79 × 10-7). Similarly, the serum metabolomic profile differed significantly between patients with liver-only metastases and with extrahepatic metastases. The change in metabolomic profile was most markedly demonstrated on GC-MS ( P = 4.75 × 10-5). Conclusions In CRC, the serum metabolomic profile changes markedly with metastasis, and site of disease also appears to affect the pattern of circulating metabolites. This novel observation may have clinical utility in enhancing staging accuracy and selecting patients for surgical or medical management. Additional studies are required to determine the sensitivity of this approach to detect subtle or occult metastatic disease.
机译:背景技术目前,大肠癌(CRC)在术前通过影像学检查进行分期,并在术后通过对可用手术标本的病理评估进行分期。但是,目前的分期方法不能准确识别隐匿性转移。这对临床管理有直接影响。尽早发现分离到肝脏的转移灶可能可以进行手术切除,而更易扩散的疾病可能最好采用姑息性化学疗法治疗。方法采用质子核磁共振( 1 H NMR)和气相色谱-质谱法对在同一三级癌症中心接受治疗的103例大肠腺癌患者的血清进行分析。 (GC-MS)。使用监督模式识别和最重要代谢物的正交偏最小二乘判别分析(O-PLS-DA)进行代谢谱分析,从而能够比较各组之间的整个样品光谱。在以下各组之间比较了从每个平台生成的代谢组学谱:局部区域CRC(N = 42);仅肝脏转移(N = 45);和肝外转移(N = 25)。结果基于 1 H NMR光谱法,与局部区域CRC相关的血清代谢组学谱与仅与肝转移相关的血清代谢组学谱不同(P = 5.10×10 -7 )和GC-MS(P = 1.79×10 -7 )。同样,仅肝转移和肝外转移患者的血清代谢组学差异也很大。代谢组学谱的变化在GC-MS上得到了最明显的证明(P = 4.75×10 -5 )。结论在CRC中,血清代谢组学特征随转移而显着变化,并且疾病部位也似乎影响循环代谢物的模式。这种新颖的观察可能在提高分期准确性和选择患者进行手术或医疗管理方面具有临床效用。需要进行进一步的研究,以确定这种方法检测细微或隐匿性转移性疾病的敏感性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号