Home > Research > Publications & Outputs > ATR microspectroscopy with multivariate analysi...
View graph of relations

ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology. / Walsh, Michael J.; Singh, Maneesh N.; Pollock, Hubert M. et al.
In: Biochemical and Biophysical Research Communications, Vol. 352, No. 1, 05.01.2007, p. 213-219.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Walsh, MJ, Singh, MN, Pollock, HM, Cooper, LJ, German, MJ, Stringfellow, HF, Fullwood, NJ, Paraskevaidis, E, Martin-Hirsch, PL & Martin, FL 2007, 'ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology.', Biochemical and Biophysical Research Communications, vol. 352, no. 1, pp. 213-219. https://doi.org/10.1016/j.bbrc.2006.11.005

APA

Walsh, M. J., Singh, M. N., Pollock, H. M., Cooper, L. J., German, M. J., Stringfellow, H. F., Fullwood, N. J., Paraskevaidis, E., Martin-Hirsch, P. L., & Martin, F. L. (2007). ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology. Biochemical and Biophysical Research Communications, 352(1), 213-219. https://doi.org/10.1016/j.bbrc.2006.11.005

Vancouver

Walsh MJ, Singh MN, Pollock HM, Cooper LJ, German MJ, Stringfellow HF et al. ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology. Biochemical and Biophysical Research Communications. 2007 Jan 5;352(1):213-219. doi: 10.1016/j.bbrc.2006.11.005

Author

Walsh, Michael J. ; Singh, Maneesh N. ; Pollock, Hubert M. et al. / ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology. In: Biochemical and Biophysical Research Communications. 2007 ; Vol. 352, No. 1. pp. 213-219.

Bibtex

@article{2a4eece47b4c45af9c5ea3b7b13a944c,
title = "ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology.",
abstract = "Although cervical cancer screening in the UK has led to reductions in the incidence of invasive disease, this programme remains flawed. We set out to examine the potential of infrared (IR) microspectroscopy to allow the profiling of cellular biochemical constituents associated with disease progression. Attenuated total reflection-Fourier Transform IR (ATR) microspectroscopy was employed to interrogate spectral differences between samples of exfoliative cervical cytology collected into liquid based cytology (LBC). These were histologically characterised as normal (n = 5), low-grade (n = 5), high-grade (n = 5) or severe dyskaryosis (? carcinoma) (n = 5). Examination of resultant spectra was coupled with principal component analysis (PCA) and subsequent linear discriminant analysis (LDA). The interrogation of LBC samples using ATR microspectroscopy with PCA–LDA facilitated the discrimination of different categories of exfoliative cytology and allowed the identification of potential biomarkers of abnormality; these occurred prominently in the IR spectral region 1200 cm−1–950 cm−1 consisting of carbohydrates, phosphate, and glycogen. Shifts in the centroids of amide I (≈1650 cm−1) and II (≈1530 cm−1) absorbance bands, indicating conformational changes to the secondary structure of intracellular proteins and associated with increasing disease progression, were also noted. This work demonstrates the potential of ATR microspectroscopy coupled with multivariate analysis to be an objective alternative to routine cytology.",
keywords = "ATR microspectroscopy, Cervical cancer, Cervical intra-epithelial neoplasia, Exfoliative cytology, Principal component analysis, Screening",
author = "Walsh, {Michael J.} and Singh, {Maneesh N.} and Pollock, {Hubert M.} and Cooper, {Leanne J.} and German, {Matthew J.} and Stringfellow, {Helen F.} and Fullwood, {Nigel J.} and Evangelos Paraskevaidis and Martin-Hirsch, {Pierre L.} and Martin, {Francis L.}",
year = "2007",
month = jan,
day = "5",
doi = "10.1016/j.bbrc.2006.11.005",
language = "English",
volume = "352",
pages = "213--219",
journal = "Biochemical and Biophysical Research Communications",
issn = "0006-291X",
publisher = "Academic Press Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - ATR microspectroscopy with multivariate analysis segregates grades of exfoliative cervical cytology.

AU - Walsh, Michael J.

AU - Singh, Maneesh N.

AU - Pollock, Hubert M.

AU - Cooper, Leanne J.

AU - German, Matthew J.

AU - Stringfellow, Helen F.

AU - Fullwood, Nigel J.

AU - Paraskevaidis, Evangelos

AU - Martin-Hirsch, Pierre L.

AU - Martin, Francis L.

PY - 2007/1/5

Y1 - 2007/1/5

N2 - Although cervical cancer screening in the UK has led to reductions in the incidence of invasive disease, this programme remains flawed. We set out to examine the potential of infrared (IR) microspectroscopy to allow the profiling of cellular biochemical constituents associated with disease progression. Attenuated total reflection-Fourier Transform IR (ATR) microspectroscopy was employed to interrogate spectral differences between samples of exfoliative cervical cytology collected into liquid based cytology (LBC). These were histologically characterised as normal (n = 5), low-grade (n = 5), high-grade (n = 5) or severe dyskaryosis (? carcinoma) (n = 5). Examination of resultant spectra was coupled with principal component analysis (PCA) and subsequent linear discriminant analysis (LDA). The interrogation of LBC samples using ATR microspectroscopy with PCA–LDA facilitated the discrimination of different categories of exfoliative cytology and allowed the identification of potential biomarkers of abnormality; these occurred prominently in the IR spectral region 1200 cm−1–950 cm−1 consisting of carbohydrates, phosphate, and glycogen. Shifts in the centroids of amide I (≈1650 cm−1) and II (≈1530 cm−1) absorbance bands, indicating conformational changes to the secondary structure of intracellular proteins and associated with increasing disease progression, were also noted. This work demonstrates the potential of ATR microspectroscopy coupled with multivariate analysis to be an objective alternative to routine cytology.

AB - Although cervical cancer screening in the UK has led to reductions in the incidence of invasive disease, this programme remains flawed. We set out to examine the potential of infrared (IR) microspectroscopy to allow the profiling of cellular biochemical constituents associated with disease progression. Attenuated total reflection-Fourier Transform IR (ATR) microspectroscopy was employed to interrogate spectral differences between samples of exfoliative cervical cytology collected into liquid based cytology (LBC). These were histologically characterised as normal (n = 5), low-grade (n = 5), high-grade (n = 5) or severe dyskaryosis (? carcinoma) (n = 5). Examination of resultant spectra was coupled with principal component analysis (PCA) and subsequent linear discriminant analysis (LDA). The interrogation of LBC samples using ATR microspectroscopy with PCA–LDA facilitated the discrimination of different categories of exfoliative cytology and allowed the identification of potential biomarkers of abnormality; these occurred prominently in the IR spectral region 1200 cm−1–950 cm−1 consisting of carbohydrates, phosphate, and glycogen. Shifts in the centroids of amide I (≈1650 cm−1) and II (≈1530 cm−1) absorbance bands, indicating conformational changes to the secondary structure of intracellular proteins and associated with increasing disease progression, were also noted. This work demonstrates the potential of ATR microspectroscopy coupled with multivariate analysis to be an objective alternative to routine cytology.

KW - ATR microspectroscopy

KW - Cervical cancer

KW - Cervical intra-epithelial neoplasia

KW - Exfoliative cytology

KW - Principal component analysis

KW - Screening

U2 - 10.1016/j.bbrc.2006.11.005

DO - 10.1016/j.bbrc.2006.11.005

M3 - Journal article

VL - 352

SP - 213

EP - 219

JO - Biochemical and Biophysical Research Communications

JF - Biochemical and Biophysical Research Communications

SN - 0006-291X

IS - 1

ER -