Targeted metabolomics in colorectal cancer: a strategic approach using standardized laboratory tests of the blood and urine.

Abstract

Background: Glycolytic markers have been detected in colorectal cancer (CRC) using advanced analytical methods.

Methods: Using commercially available assays, by-products of anaerobic metabolism were prospectively measured in the blood and urine of 20 patients with metastatic colorectal cancer (mCRC) and 20 patients with local disease. Twenty-four-hour urine citrate, plasma lactate, ketones, venous blood gas, anion gap, and osmolar gap were investigated. Results of patients with metastatic and local CRC were compared using two-sample t-tests or equivalent nonparametric tests. In addition, plasma total CO₂ concentrations in our local hospital (5,931 inpatients and 1,783 outpatients) were compared retrospectively with those in our dedicated cancer center (1,825 outpatients) over 1 year.

Results: The average venous pCO₂ was higher in patients with mCRC (50.2 mmHg; standard deviation [SD]=9.36) compared with those with local disease (42.8 mmHg; SD=8.98), p=0.045. Calculated serum osmolarity was higher in mCRC and attributed to concomitant sodium and urea elevations. In our retrospective analysis, plasma total CO₂ concentrations (median=27 mmol/L) were higher in cancer patients compared to both hospital inpatients (median=23 mmol/L) and outpatients (median=24 mmol/L), p<0.0001.

Conclusion: Patients with mCRC had higher venous pCO₂ levels than those with local disease. Although causation cannot be established, we hypothesize that pCO₂ elevation may stem from a perturbed metabolism in mCRC.