Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/10164
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dc.contributor.authorWazir, U-
dc.contributor.authorSharma, AK-
dc.contributor.authorMokbel, K-
dc.contributor.authorAhmed, MH-
dc.contributor.authorBridger, JM-
dc.contributor.authorHarvey, A-
dc.contributor.authorJiang, WG-
dc.date.accessioned2015-02-09T16:12:08Z-
dc.date.available2013-
dc.date.available2015-02-09T16:12:08Z-
dc.date.issued2013-
dc.identifier.citationCellular and Molecular Biology Letters, 18(4): 1 - 17, (December 2013)en_US
dc.identifier.issn1425-8153-
dc.identifier.issn1689-1392-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/10164-
dc.identifier.urihttp://www.degruyter.com/view/j/cmble.2013.18.issue-4/s11658-013-0109-9/s11658-013-0109-9.xml-
dc.description.abstractLamin A/C (LMNA), lamin B1 (LMNB1) and lamin B receptor (LBR) have key roles in nuclear structural integrity and chromosomal stability. In this study, we have studied the relationships between the mRNA expressions of A-type lamins, LMNB1 and LBR and the clinicopathological parameters in human breast cancer. Samples of breast cancer tissues (n = 115) and associated non-cancerous tissue (ANCT; n = 30) were assessed using reverse transcription and quantitative PCR. Transcript levels were correlated with clinicopathological data. Higher levels of A-type lamins and LMNB1 mRNA expression were seen in ANCT. Higher lamin A/C expression was associated with the early clinical stage (TNM1 vs. TNM3 - 13 vs. 0.21; p = 0.0515), with better clinical outcomes (disease-free survival vs. mortality - 11 vs. 1; p = 0.0326), and with better overall (p = 0.004) and disease-free survival (p = 0.062). The expression of LMNB1 declined with worsening clinical outcome (disease-free vs. mortalities - 0.0011 vs. 0.000; p = 0.0177). LBR mRNA expression was directly associated with tumor grade (grade 1 vs. grade 3-0.00 vs. 0.00; p = 0.0479) and Nottingham Prognostic Index (NPI1 vs. NPI3-0.00 vs. 0.00; p = 0.0551). To the best of our knowledge, this is the first study to suggest such a role for A-type lamins, lamin B1 and LBR in human breast cancer, identifying an important area for further research. © 2013 Versita Warsaw and Springer-Verlag Wien.en_US
dc.description.sponsorshipThis study was funded by grants from the Breast Cancer Hope Foundation (London, UK) and the Gordon Memorial Trust Fund to MHA.en_US
dc.format.extent1 - 17-
dc.format.extent1 - 17-
dc.language.isoenen_US
dc.publisherWalter de Gruyter GmbHen_US
dc.subjectLamin A/Cen_US
dc.subjectLamin Ben_US
dc.subjectLamin B receptoren_US
dc.subjectBreast canceren_US
dc.subjectqPCRen_US
dc.subjectChromosomal instabilityen_US
dc.subjectCell senescenceen_US
dc.subjectCell cycleen_US
dc.subjectDNA repairen_US
dc.subjectAgeingen_US
dc.titleThe clinicopathological significance of lamin A/C, lamin B1 and lamin B receptor mRNA expression in human breast canceren_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.2478/s11658-013-0109-9-
dc.relation.isPartOfCellular and Molecular Biology Letters-
dc.relation.isPartOfCellular and Molecular Biology Letters-
pubs.organisational-data/Brunel-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences/Dept of Life Sciences-
pubs.organisational-data/Brunel/Brunel Staff by College/Department/Division/College of Health and Life Sciences/Dept of Life Sciences/Biological Sciences-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme/Institute of Environmental, Health and Societies-
pubs.organisational-data/Brunel/Brunel Staff by Institute/Theme/Institute of Environmental, Health and Societies/Synthetic Biology-
pubs.organisational-data/Brunel/University Research Centres and Groups-
pubs.organisational-data/Brunel/University Research Centres and Groups/School of Health Sciences and Social Care - URCs and Groups-
pubs.organisational-data/Brunel/University Research Centres and Groups/School of Health Sciences and Social Care - URCs and Groups/Brunel Institute for Ageing Studies-
pubs.organisational-data/Brunel/University Research Centres and Groups/School of Health Sciences and Social Care - URCs and Groups/Brunel Institute of Cancer Genetics and Pharmacogenomics-
pubs.organisational-data/Brunel/University Research Centres and Groups/School of Health Sciences and Social Care - URCs and Groups/Centre for Systems and Synthetic Biology-
Appears in Collections:Dept of Life Sciences Research Papers

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