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10.4143/crt.2017.275

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C6056971!6056971 !28934848
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suck abstract from ncbi


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pmid28934848
      Cancer+Res+Treat 2018 ; 50 (3 ): 883-893
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  • Profiling of Serum Metabolites Using MALDI-TOF and Triple-TOF Mass Spectrometry to Develop a Screen for Ovarian Cancer #MMPMID28934848
  • Lee JH ; Kim YH ; Kim KH ; Cho JY ; Woo SM ; Yoo BC ; Kim SC
  • Cancer Res Treat 2018[Jul]; 50 (3 ): 883-893 PMID28934848 show ga
  • PURPOSE: We sought to develop a matrix assisted laser desorption ionization-time of flight (MALDI-TOF)-based, ovarian cancer (OVC), low-mass-ion discriminant equation (LOME) and to evaluate a possible supportive role for triple-TOF mass analysis in identifying metabolic biomarkers. MATERIALS AND METHODS: A total of 114 serum samples from patients with OVC and benign ovarian tumors were subjected to MALDI-TOF analysis and a total of 137 serum samples from healthy female individuals and patients with OVC, colorectal cancer, hepatobiliary cancer, and pancreatic cancer were subjected to triple-TOF analysis. An OVC LOME was constructed by reference to the peak intensity ratios of discriminatory low-mass ion (LMI) pairs. Triple-TOF analysiswas used to select and identify metabolic biomarkers for OVC screening. RESULTS: Three OVC LOMEs were finally constructed using discriminatory LMI pairs (137.1690 and 84.4119 m/z; 496.5022 and 709.7642 m/z; and 524.5614 and 709.7642 m/z); all afforded accuracies of > 90%. The LMIs at 496.5022 m/z and 524.5614 m/z were those of lysophosphatidylcholine (LPC) 16:0 and LPC 18:0. Triple-TOF analysis selected seven discriminative LMIs; each LMI had a specificity > 90%. Of the seven LMIs, fourwith a 137.0455 m/z ion atretention times of 2.04-3.14 minuteswere upregulated in sera from OVC patients; the ion was identified as that derived from hypoxanthine. CONCLUSION: MALDI-TOF-based OVC LOMEs combined with triple-TOF-based OVC metabolic biomarkers allow reliable OVC screening; the techniques are mutually complementary both quantitatively and qualitatively.
  • |Adult [MESH]
  • |Aged [MESH]
  • |Aged, 80 and over [MESH]
  • |Biomarkers, Tumor/*blood [MESH]
  • |Case-Control Studies [MESH]
  • |Early Detection of Cancer/*methods [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Metabolome [MESH]
  • |Middle Aged [MESH]
  • |Ovarian Neoplasms/blood/*diagnosis [MESH]
  • |Principal Component Analysis [MESH]


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