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    FTIR-based spectroscopic analysis in the identification of clinically aggressive prostate cancer.

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    Authors
    Baker, Matthew J
    Gazi, Ehsan
    Brown, Michael D
    Shanks, Jonathan H
    Gardner, Peter
    Clarke, Noel W
    Affiliation
    Manchester Interdisciplinary Biocentre, Centre for Instrumentation and Analytical Science, School of Chemical Engineering and Analytical Science, The University of Manchester, Manchester, M1 7DN, UK. M.J.Baker@manchester.ac.uk
    Issue Date
    2008-12-02
    
    Metadata
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    Abstract
    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.
    Citation
    FTIR-based spectroscopic analysis in the identification of clinically aggressive prostate cancer. 2008, 99 (11):1859-66 Br. J. Cancer
    Journal
    British Journal of Cancer
    URI
    http://hdl.handle.net/10541/67950
    DOI
    10.1038/sj.bjc.6604753
    PubMed ID
    18985044
    Type
    Article
    Language
    en
    ISSN
    1532-1827
    ae974a485f413a2113503eed53cd6c53
    10.1038/sj.bjc.6604753
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research
    Pathology
    Urological Oncology
    School of Cancer and Imaging Sciences

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