2018
DOI: 10.1038/s41598-018-33417-8
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Raman spectroscopic detection of high-grade cervical cytology: Using morphologically normal appearing cells

Abstract: This study aims to detect high grade squamous intraepithelial cells (HSIL) by investigating HSIL associated biochemical changes in morphologically normal appearing intermediate and superficial cells using Raman spectroscopy. Raman spectra (n = 755) were measured from intermediate and superficial cells from negative cytology ThinPrep specimens (n = 18) and from morphologically normal appearing intermediate and superficial cells from HSIL cytology ThinPrep specimens (n = 17). The Raman data was subjected to mult… Show more

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Cited by 30 publications
(37 citation statements)
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“…The mean Raman spectra and LV1 loadings showed that the discrimination was mostly based around increased nucleic acids (727, 781, 826, 1485, and 1580 cm −1 ), decreased glycogen (482, 852, 937, 1082, 1123, 1334, and 1380 cm −1 ), and changes in protein features (1152, 1240, 1450, 1640, and 1670 cm −1 ), indicating increased proliferation and altered protein expression due to the overexpression of E6/E7 viral proteins in the samples with a transcriptionally active HPV infection. These discriminating spectral features are consistent with previous studies on exfoliated cells showing discrimination between samples with negative cytology and HSIL cytology [ 25 , 27 , 28 , 30 , 34 ] and between samples with negative cytology and HPV DNA-positive HSIL samples [ 29 ]. PLSDA classification with LOPOCV achieved a sensitivity of 88% and a specificity of 88% in distinguishing non-transcriptionally active HPV infection from transcriptionally active HPV infection.…”
Section: Discussionsupporting
confidence: 91%
“…The mean Raman spectra and LV1 loadings showed that the discrimination was mostly based around increased nucleic acids (727, 781, 826, 1485, and 1580 cm −1 ), decreased glycogen (482, 852, 937, 1082, 1123, 1334, and 1380 cm −1 ), and changes in protein features (1152, 1240, 1450, 1640, and 1670 cm −1 ), indicating increased proliferation and altered protein expression due to the overexpression of E6/E7 viral proteins in the samples with a transcriptionally active HPV infection. These discriminating spectral features are consistent with previous studies on exfoliated cells showing discrimination between samples with negative cytology and HSIL cytology [ 25 , 27 , 28 , 30 , 34 ] and between samples with negative cytology and HPV DNA-positive HSIL samples [ 29 ]. PLSDA classification with LOPOCV achieved a sensitivity of 88% and a specificity of 88% in distinguishing non-transcriptionally active HPV infection from transcriptionally active HPV infection.…”
Section: Discussionsupporting
confidence: 91%
“…The resulting LD scores matrix “ Z ” represents compactly the original data features, “ ” and differentiates one class from another very efficiently. Detail of LDA can be found in 58 60 .…”
Section: Methodsmentioning
confidence: 99%
“…The ThinPrep standard, including the use of associated fixatives and glass slides, has previously been shown to be compatible with Raman micro-spectroscopy. [5,7,12,24,30] HeLa cells were selected for this initial investigation due to their well known morphology and were prepared as described in Section 3.1.1 and imaged using an IX81 fluorescence microscope as described in Section 3.2. In Fig.1 (a) the live cells are shown in medium. The image was slightly defocused by displacing the sample approximately 1μm from the focal plane, and oblique illumination was used in order to improve visualisation of cell boundaries.…”
Section: Automationmentioning
confidence: 99%