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Raman spectroscopic techniques to detect ovarian cancer biomarkers in blood plasma.
Paraskevaidi, Maria; Ashton, Katherine M; Stringfellow, Helen F; Wood, Nicholas J; Keating, Patrick J; Rowbottom, Anthony W; Martin-Hirsch, Pierre L; Martin, Francis L.
Afiliação
  • Paraskevaidi M; School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston PR1 2HE, UK. Electronic address: mparaskevaidi@uclan.ac.uk.
  • Ashton KM; Pathology Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Stringfellow HF; Pathology Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Wood NJ; Department of Obstetrics and Gynaecology, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Keating PJ; Department of Obstetrics and Gynaecology, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Rowbottom AW; Immunology Laboratory, Pathology Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Martin-Hirsch PL; Department of Obstetrics and Gynaecology, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
  • Martin FL; School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston PR1 2HE, UK. Electronic address: flmartin@uclan.ac.uk.
Talanta ; 189: 281-288, 2018 Nov 01.
Article em En | MEDLINE | ID: mdl-30086919
ABSTRACT
Robust diagnosis of ovarian cancer is crucial to improve patient outcomes. The lack of a single and accurate diagnostic approach necessitates the advent of novel methods in the field. In the present study, two spectroscopic techniques, Raman and surface-enhanced Raman spectroscopy (SERS) using silver nanoparticles, have been employed to identify signatures linked to cancer in blood. Blood plasma samples were collected from 27 patients with ovarian cancer and 28 with benign gynecological conditions, the majority of which had a prolapse. Early ovarian cancer cases were also included in the cohort (n = 17). The derived information was processed to account for differences between cancerous and healthy individuals and a support vector machine (SVM) algorithm was applied for classification. A subgroup analysis using CA-125 levels was also conducted to rule out that the observed segregation was due to CA-125 differences between patients and controls. Both techniques provided satisfactory diagnostic accuracy for the detection of ovarian cancer, with spontaneous Raman achieving 94% sensitivity and 96% specificity and SERS 87% sensitivity and 89% specificity. For early ovarian cancer, Raman achieved sensitivity and specificity of 93% and 97%, respectively, while SERS had 80% sensitivity and 94% specificity. Five spectral biomarkers were detected by both techniques and could be utilised as a panel of markers indicating carcinogenesis. CA-125 levels did not seem to undermine the high classification accuracies. This minimally invasive test may provide an alternative diagnostic and screening tool for ovarian cancer that is superior to other established blood-based biomarkers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Análise Espectral Raman / Análise Química do Sangue / Biomarcadores Tumorais Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Análise Espectral Raman / Análise Química do Sangue / Biomarcadores Tumorais Idioma: En Ano de publicação: 2018 Tipo de documento: Article