Baker, Matthew James, Gazi, E, Brown, M D, Shanks, J H, Gardner, P and Clarke, N W (2008) FTIR-based spectroscopic analysis in the identification of clinically aggressive prostate cancer. British Journal of Cancer, 99 (11). pp. 1859-1866. ISSN 0007-0920
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Available under License Creative Commons Attribution Non-commercial Share Alike.
Official URL: http://dx.doi.org/10.1038/sj.bjc.6604753
Fourier transform infrared (FTIR) spectroscopy is a vibrational spectroscopic technique that uses infrared radiation to vibrate molecular bonds within the sample that absorbs it. As different samples contain different molecular bonds or different configurations of molecular bonds, FTIR allows us to obtain chemical information on molecules within the sample. Fourier transform infrared microspectroscopy in conjunction with a principal component-discriminant function analysis (PC-DFA) algorithm was applied to the grading of prostate cancer (CaP) tissue specimens. The PC-DFA algorithm is used alongside the established diagnostic measures of Gleason grading and the tumour/node/metastasis system. Principal component-discriminant function analysis improved the sensitivity and specificity of a three-band Gleason score criterion diagnosis previously reported by attaining an overall sensitivity of 92.3% and specificity of 99.4%. For the first time, we present the use of a two-band criterion showing an association of FTIR-based spectral characteristics with clinically aggressive behaviour in CaP manifest as local and/or distal spread. This paper shows the potential for the use of spectroscopic analysis for the evaluation of the biopotential of CaP in an accurate and reproducible manner.
|Uncontrolled Keywords (separate with ;):||FTIR microspectroscopy; prostate cancer; molecular diagnosis; Gleason grade; PC-DFA; infrared spectroscopy|
|Subjects:||Physical sciences > Chemistry|
|Schools:||Faculty of Science and Technology > School of Forensic and Applied Sciences|
|Deposited By:||Helen Cooper|
|Deposited On:||07 Feb 2012 15:05|
|Last Modified:||24 Oct 2016 15:09|
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