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dc.contributor.authorGosling, S
dc.contributor.authorCalabrese, D
dc.contributor.authorNallala, J
dc.contributor.authorGreenwood, C
dc.contributor.authorPinder, S
dc.contributor.authorKing, L
dc.contributor.authorMarks, J
dc.contributor.authorPinto, D
dc.contributor.authorLynch, T
dc.contributor.authorLyburn, ID
dc.contributor.authorHwang, ES
dc.contributor.authorGrand Challenge Precision Consortium
dc.contributor.authorRogers, K
dc.contributor.authorStone, N
dc.date.accessioned2022-05-10T09:19:53Z
dc.date.issued2022-03-21
dc.date.updated2022-05-09T15:24:30Z
dc.description.abstractDuctal carcinoma in situ (DCIS) is frequently associated with breast calcification. This study combines multiple analytical techniques to investigate the heterogeneity of these calcifications at the micrometre scale. X-ray diffraction, scanning electron microscopy and Raman and Fourier-transform infrared spectroscopy were used to determine the physicochemical and crystallographic properties of type II breast calcifications located in formalin fixed paraffin embedded DCIS breast tissue samples. Multiple calcium phosphate phases were identified across the calcifications, distributed in different patterns. Hydroxyapatite was the dominant mineral, with magnesium whitlockite found at the calcification edge. Amorphous calcium phosphate and octacalcium phosphate were also identified close to the calcification edge at the apparent mineral/matrix barrier. Crystallographic features of hydroxyapatite also varied across the calcifications, with higher crystallinity centrally, and highest carbonate substitution at the calcification edge. Protein was also differentially distributed across the calcification and the surrounding soft tissue, with collagen and β-pleated protein features present to differing extents. Combination of analytical techniques in this study was essential to understand the heterogeneity of breast calcifications and how this may link crystallographic and physicochemical properties of calcifications to the surrounding tissue microenvironment.en_GB
dc.description.sponsorshipCancer Research UKen_GB
dc.description.sponsorshipKWF Kankerbestrijdingen_GB
dc.format.extent1641-1654
dc.format.mediumElectronic
dc.identifier.citationVol. 147(8), pp. 1641-1654en_GB
dc.identifier.doihttps://doi.org/10.1039/d1an01548f
dc.identifier.grantnumberC38317/A24043en_GB
dc.identifier.urihttp://hdl.handle.net/10871/129574
dc.identifierORCID: 0000-0002-9473-5782 (Nallala, Jayakrupakar)
dc.identifierORCID: 0000-0001-5603-3731 (Stone, Nicholas)
dc.identifierScopusID: 7202511172 (Stone, Nicholas)
dc.language.isoenen_GB
dc.publisherRoyal Society of Chemistry (RSC)en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/35311860en_GB
dc.rights© The Royal Society of Chemistry 2022. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.en_GB
dc.titleA multi-modal exploration of heterogeneous physico-chemical properties of DCIS breast microcalcificationsen_GB
dc.typeArticleen_GB
dc.date.available2022-05-10T09:19:53Z
dc.identifier.issn0003-2654
exeter.place-of-publicationEngland
dc.descriptionThis is the final version. Available on open access from the Royal Society of Chemistry via the DOI in this recorden_GB
dc.identifier.eissn1364-5528
dc.identifier.journalAnalysten_GB
dc.relation.ispartofAnalyst, 147(8)
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/en_GB
dcterms.dateAccepted2022-01-24
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-03-21
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-05-10T09:12:05Z
refterms.versionFCDVoR
refterms.dateFOA2022-05-10T09:20:17Z
refterms.panelBen_GB
refterms.dateFirstOnline2022


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© The Royal Society of Chemistry 2022. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Except where otherwise noted, this item's licence is described as © The Royal Society of Chemistry 2022. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.