Identification of potential metabolic biomarkers of rectal cancer and of the effect of neoadjuvant radiochemotherapy

PLoS One. 2021 Apr 22;16(4):e0250453. doi: 10.1371/journal.pone.0250453. eCollection 2021.

Abstract

We report a pilot study on the feasibility of determinations of circulating levels of paraoxonase-1 (PON1) and compounds related to energy metabolism as biomarkers for the evaluation of patients with rectal cancer (RC), and the effects produced by neoadjuvant radiochemotherapy (NRCT). We studied 32 patients treated with radiotherapy plus capecitabine concomitant chemotherapy and 48 control subjects. We identified pre-NRCT PON1 and α-ketoglutarate as the parameters that best discriminated between RC patients and the control group. Receiver operating characteristics analysis of the combination of the two parameters showed an area under the curve (AUC) of 0.918. Moreover, patients who presented a pathological complete response (pCR) to treatment had lower plasma pre-NRCT valine concentrations (AUC of 0.826). Patients who had a relapse had lower concentrations of succinate (AUC of 0.833). The results of the present study illustrate the usefulness of investigating alterations in oxidative stress and metabolism in RC. Due to the small number of patients studied, our results must be considered preliminary, but they suggest that the determination of circulating levels of PON1 and α-ketoglutarate might be a valuable tool for the early diagnosis of RC, while the determination of valine and succinate might effectively predict pCR and the appearance of relapse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aryldialkylphosphatase / genetics*
  • Aryldialkylphosphatase / metabolism
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Chemoradiotherapy / adverse effects
  • Female
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Ketoglutaric Acids / blood
  • Male
  • Middle Aged
  • Neoadjuvant Therapy / adverse effects
  • Neoplasm Recurrence, Local / drug therapy
  • Neoplasm Recurrence, Local / genetics*
  • Neoplasm Recurrence, Local / metabolism
  • Neoplasm Recurrence, Local / radiotherapy
  • Rectal Neoplasms / drug therapy
  • Rectal Neoplasms / genetics*
  • Rectal Neoplasms / metabolism
  • Rectal Neoplasms / radiotherapy
  • Treatment Outcome

Substances

  • Biomarkers, Tumor
  • Ketoglutaric Acids
  • Aryldialkylphosphatase
  • PON1 protein, human

Grants and funding

This research was funded by ASSOCIACIÓ ONCOLÒGICA DR. AMADEU PELEGRÍ, grant number AODAP-2017 (M.A. and J,C.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.