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dc.contributor.authorBaker, R
dc.contributor.authorRogers, KD
dc.contributor.authorShepherd, N
dc.contributor.authorStone, N
dc.date.accessioned2017-02-09T09:20:39Z
dc.date.issued2010-09-14
dc.description.abstractBACKGROUND: Breast microcalcifications are key diagnostically significant radiological features for localisation of malignancy. This study explores the hypothesis that breast calcification composition is directly related to the local tissue pathological state. METHODS: A total of 236 human breast calcifications from 110 patients were analysed by mid-Fouries transform infrared (FTIR) spectroscopy from three different pathology types (112 invasive carcinoma (IC), 64 in-situ carcinomas and 60 benign). The biochemical composition and the incorporation of carbonate into the hydroxyapatite lattice of the microcalcifications were studied by infrared microspectroscopy. This allowed the spectrally identified composition to be directly correlated with the histopathology grading of the surrounding tissue. RESULTS: The carbonate content of breast microcalcifications was shown to significantly decrease when progressing from benign to malignant disease. In this study, we report significant correlations (P<0.001) between microcalcification chemical composition (carbonate content and protein matrix : mineral ratios) and distinct pathology grades (benign, in-situ carcinoma and ICs). Furthermore, a significant correlation (P<0.001) was observed between carbonate concentrations and carcinoma in-situ sub-grades. Using the two measures of pathology-specific calcification composition (carbonate content and protein matrix : mineral ratios) as the inputs to a two-metric discriminant model sensitivities of 79, 84 and 90% and specificities of 98, 82 and 96% were achieved for benign, ductal carcinoma in situ and invasive malignancies, respectively. CONCLUSIONS: We present the first demonstration of a direct link between the chemical nature of microcalcifications and the grade of the pathological breast disease. This suggests that microcalcifications have a significant association with cancer progression, and could be used for future objective analytical classification of breast pathology. A simple two-metric model has been demonstrated, more complex spectral analysis may yeild greater discrimination performance. Furthermore there appears to be a sequential progression of calcification composition.en_GB
dc.description.sponsorshipProfessor Nicholas Stone is supported by a National Institute of Health Research (NIHR) Career Scientist (Senior) Research Fellowship. Rebecca Baker performed the study, performed the data analysis and wrote the paper. Keith Rogers designed and supervised the study and wrote the paper. Neil Shepherd provided expert histopathology support and discussion. Nicholas Stone designed and supervised the study and wrote the paper. The authors declare no conflicts of interest. Ethical approval for this study was provided by the Gloucestershire Local Research Ethics Committee, UK.en_GB
dc.identifier.citationVol. 103, pp. 1034 - 1039en_GB
dc.identifier.doi10.1038/sj.bjc.6605873
dc.identifier.other6605873
dc.identifier.urihttp://hdl.handle.net/10871/25720
dc.language.isoenen_GB
dc.publisherCancer Research UKen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/20842116en_GB
dc.rightsThis work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/en_GB
dc.subjectBreast Diseasesen_GB
dc.subjectBreast Neoplasmsen_GB
dc.subjectCalcinosisen_GB
dc.subjectCarbonatesen_GB
dc.subjectCarcinomaen_GB
dc.subjectCarcinoma in Situen_GB
dc.subjectCarcinoma, Ductal, Breasten_GB
dc.subjectFemaleen_GB
dc.subjectHumansen_GB
dc.titleNew relationships between breast microcalcifications and cancer.en_GB
dc.typeArticleen_GB
dc.date.available2017-02-09T09:20:39Z
dc.identifier.issn0007-0920
exeter.place-of-publicationEnglanden_GB
dc.descriptionPublisheden_GB
dc.descriptionJournal Articleen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.descriptionThis is the final version of the article. Available from Cancer Research UK via the DOI in this record.en_GB
dc.identifier.eissn1532-1827
dc.identifier.journalBritish Journal of Canceren_GB


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