4.6 Article

Exploring Serum NMR-Based Metabolomic Fingerprint of Colorectal Cancer Patients: Effects of Surgery and Possible Associations with Cancer Relapse

期刊

APPLIED SCIENCES-BASEL
卷 11, 期 23, 页码 -

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MDPI
DOI: 10.3390/app112311120

关键词

metabolomics; colorectal cancer; nuclear magnetic resonance; surgery; relapse

资金

  1. Fondazione Pitigliani per la lotta contro itumori ONLUS
  2. AIRC fellowship for Italy

向作者/读者索取更多资源

The study investigated the changes in preoperative and postoperative serum metabolomic fingerprints of CRC patients and found that some metabolic changes may be associated with cancer relapse. Certain metabolites such as pyruvate and HDL-related parameters appear to play important roles in discriminating between preoperative and postoperative serum samples of CRC patients.
Background: Colorectal cancer (CRC) is the fourth most commonly diagnosed and third most deadly cancer worldwide. Surgery is the main treatment option for early disease; however, a relevant proportion of CRC patients relapse. Here, variations among preoperative and postoperative serum metabolomic fingerprint of CRC patients were studied, and possible associations between metabolic variations and cancer relapse were explored. Methods: A total of 41 patients with stage I-III CRC, planned for radical resection, were enrolled. Serum samples, collected preoperatively (t0) and 4-6 weeks after surgery before the start of any treatment (t1), were analyzed via NMR spectroscopy. NMR data were analyzed using multivariate and univariate statistical approaches. Results: Serum metabolomic fingerprints show differential clustering between t0 and t1 (82-85% accuracy). Pyruvate, HDL-related parameters, acetone, and 3-hydroxybutyrate appear to be the major players in this discrimination. Eight out of the 41 CRC patients enrolled developed cancer relapse. Postoperative, relapsed patients show an increase of pyruvate and HDL-related parameters, and a decrease of Apo-A1 Apo-B100 ratio and VLDL-related parameters. Conclusions: Surgery significantly alters the metabolomic fingerprint of CRC patients. Some metabolic changes seem to be associated with the development of cancer relapse. These data, if validated in a larger cohort, open new possibilities for risk stratification in patients with early-stage CRC.

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