Targeted metabolomics detects a putatively diagnostic signature in plasma and dried blood spots from head and neck paraganglioma patients.
Simone De FabritiisSilvia ValentinuzziGianluca PirasIlaria CicaliniDamiana PieragostinoSara PagottoSilvia PercontiMirco ZucchelliAlberto SchenaElisa TaschinGloria Simona BerteşteanuDiana Liberata EspositoAntonio StiglianoVincenzo De LaurenziFrancesca SchiaviMario SannaPiero Del BoccioRenato Mariani-CostantiniRenato Mariani-CostantiniPublished in: Oncogenesis (2023)
Head and neck paragangliomas (HNPGLs), rare chemoresistant tumors curable only with surgery, are strongly influenced by genetic predisposition, hence patients and relatives require lifetime follow-up with MRI and/or PET-CT because of de novo disease risk. This entails exposure to electromagnetic/ionizing radiation, costs, and organizational challenges, because patients and relatives are scattered far from reference centers. Simplified first-line screening strategies are needed. We employed flow injection analysis tandem mass spectrometry, as used in newborn metabolic screening, to compare the plasma metabolic profile of HNPGL patients (59 samples, 56 cases) and healthy controls (24 samples, 24 cases). Principal Component Analysis (PCA) and Partial Least Discriminant Analysis (PLS-DA) highlighted a distinctive HNPGL signature, likely reflecting the anaplerotic conversion of the TCA cycle to glutaminolysis and catabolism of branched amino acids, DNA damage and deoxyadenosine (dAdo) accumulation, impairment of fatty acid oxidation, switch towards the Warburg effect and proinflammatory lysophosphatidylcholines (LPCs) signaling. Statistical analysis of the metabolites that most impacted on PLS-DA was extended to 10 acoustic neuroma and 2 cholesteatoma patients, confirming significant differences relative to the HNPGL plasma metabolomic profile. The best confusion matrix from the ROC curve built on 2 metabolites, dAdo and C26:0-LPC, provided specificity of 94.29% and sensitivity of 89.29%, with positive and negative predictive values of 96.2% and 84.6%, respectively. Analysis of dAdo and C26:0-LPC levels in dried venous and capillary blood confirmed that dAdo, likely deriving from 2'-deoxy-ATP accumulated in HNPGL cells following endogenous genotoxic damage, efficiently discriminated HNPGL patients from healthy controls and acoustic neuroma/cholesteatoma patients on easily manageable dried blood spots.
Keyphrases
- end stage renal disease
- chronic kidney disease
- ejection fraction
- newly diagnosed
- dna damage
- prognostic factors
- ms ms
- pet ct
- gene expression
- patient reported outcomes
- induced apoptosis
- dna methylation
- magnetic resonance
- mass spectrometry
- signaling pathway
- genome wide
- percutaneous coronary intervention
- endoplasmic reticulum stress
- tandem mass spectrometry
- fatty acid
- ultrasound guided
- liquid chromatography
- pi k akt
- diffusion weighted imaging