Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26750
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dc.contributor.authorBox, C-
dc.contributor.authorPennington, C-
dc.contributor.authorHare, S-
dc.contributor.authorPorter, S-
dc.contributor.authorEdwards, D-
dc.contributor.authorEccles, S-
dc.contributor.authorCrompton, M-
dc.contributor.authorHarvey, A-
dc.date.accessioned2023-06-29T12:29:57Z-
dc.date.available2023-06-29T12:29:57Z-
dc.date.issued2023-06-28-
dc.identifierORCID iDs: Carol Box https://orcid.org/0000-0002-8919-8724; Caroline Pennington https://orcid.org/0009-0004-1068-9515; Amanda Harvey https://orcid.org/0000-0003-0257-641X.-
dc.identifier10757-
dc.identifier.citationBox, C. et al. (2023) 'Brk/PTK6 and Involucrin Expression May Predict Breast Cancer Cell Responses to Vitamin D', International Journal of Molecular Sciences, 2023, 24, 10757, pp. 1 - 14. doi: 10.3390/ijms241310757.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/26750-
dc.descriptionData Availability Statement: No datasets were generated during this studyen_US
dc.description.abstractCopyright © 2023 by the authors. The process of human embryonic mammary development gives rise to the structures in which mammary cells share a developmental lineage with skin epithelial cells such as keratinocytes. As some breast carcinomas have previously been shown to express high levels of involucrin, a marker of keratinocyte differentiation, we hypothesised that some breast tumours may de-differentiate to a keratinocyte-derived ‘evolutionary history’. To confirm our hypothesis, we investigated the frequency of involucrin expression along with that of Brk, a tyrosine kinase expressed in up to 86% of breast carcinomas whose normal expression patterns are restricted to differentiating epithelial cells, most notably those in the skin (keratinocytes) and the gastrointestinal tract. We found that involucrin, a keratinocyte differentiation marker, was expressed in a high proportion (78%) of breast carcinoma samples and cell lines. Interestingly, tumour samples found to express high levels of involucrin were also shown to express Brk. 1,25-dihydroxyvitamin D3, a known differentiation agent and potential anti-cancer agent, decreased proliferation in the breast cancer cell lines that expressed both involucrin and Brk, whereas the Brk/involucrin negative cell lines tested were less susceptible. In addition, responses to 1,25-dihydroxyvitamin D3 were not correlated with vitamin D receptor expression. These data contribute to the growing body of evidence suggesting that cellular responses to 1,25-dihydroxyvitamin D3 are potentially independent of vitamin D receptor status and provide an insight into potential markers, such as Brk and/or involucrin that could predict therapeutic responses to 1,25-dihydroxyvitamin D3.en_US
dc.description.sponsorshipThis work was supported primarily by project grants from the Breast Cancer Campaign (2006NovPR19 awarded to MRC/SE/AH) and the EU Framework Programme 6 Cancer Degradome project (LSHC-CT-2003-503297). The authors acknowledge NHS funding to the NIHR Biomedical Research Centre.en_US
dc.format.extent1 - 14-
dc.format.mediumElectronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.rightsCopyright © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject1,25-dihydroxyvitamin D3en_US
dc.subjectbreast canceren_US
dc.subjectbreast tumour kinase (Brk)en_US
dc.subjectprotein tyrosine kinase 6 (PTK6)en_US
dc.subjectdifferentiationen_US
dc.subjectinvolucrinen_US
dc.titleBrk/PTK6 and Involucrin Expression May Predict Breast Cancer Cell Responses to Vitamin Den_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3390/ijms241310757-
dc.relation.isPartOfInternational Journal of Molecular Sciences-
pubs.publication-statusPublished online-
pubs.volume24-
dc.identifier.eissn1422-0067-
dc.rights.holderThe authors-
Appears in Collections:Dept of Life Sciences Research Papers

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