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dc.contributor.authorJames, Louise A
dc.contributor.authorMitchell, Erika L D
dc.contributor.authorMenasce, Lia P
dc.contributor.authorVarley, Jennifer
dc.date.accessioned2010-03-24T15:29:09Z
dc.date.available2010-03-24T15:29:09Z
dc.date.issued1997-03-06
dc.identifier.citationComparative genomic hybridisation of ductal carcinoma in situ of the breast: identification of regions of DNA amplification and deletion in common with invasive breast carcinoma. 1997, 14 (9):1059-65 Oncogeneen
dc.identifier.issn0950-9232
dc.identifier.pmid9070654
dc.identifier.doi10.1038/sj.onc.1200923
dc.identifier.urihttp://hdl.handle.net/10541/94907
dc.description.abstractComparative genomic hybridisation has been used to map copy number changes in nine cases of ductal carcinoma in situ of the breast obtained from wax-embedded archive material. A wide variety of abnormalities were detected including gain of regions of 1q, 17q, 19q, 20p and 20q and loss on 13q, 14q, 17p, 16q and 22q. Amplification of areas on 10p, 8q and 20q were also observed. Chromosomal alterations were more frequent in higher grade DCIS and closely resemble those previously detected in invasive breast cancer using the same technique. These data provide strong molecular support for the view that DCIS is a precursor lesion of invasive breast carcinoma.
dc.language.isoenen
dc.subjectBreast Canceren
dc.subject.meshAged
dc.subject.meshBreast Neoplasms
dc.subject.meshCarcinoma in Situ
dc.subject.meshCarcinoma, Ductal, Breast
dc.subject.meshFemale
dc.subject.meshGene Amplification
dc.subject.meshGene Deletion
dc.subject.meshHumans
dc.subject.meshMiddle Aged
dc.subject.meshNucleic Acid Hybridization
dc.subject.meshRetrospective Studies
dc.titleComparative genomic hybridisation of ductal carcinoma in situ of the breast: identification of regions of DNA amplification and deletion in common with invasive breast carcinoma.en
dc.typeArticleen
dc.contributor.departmentCRC Department of Cancer Genetics, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester.en
dc.identifier.journalOncogeneen
html.description.abstractComparative genomic hybridisation has been used to map copy number changes in nine cases of ductal carcinoma in situ of the breast obtained from wax-embedded archive material. A wide variety of abnormalities were detected including gain of regions of 1q, 17q, 19q, 20p and 20q and loss on 13q, 14q, 17p, 16q and 22q. Amplification of areas on 10p, 8q and 20q were also observed. Chromosomal alterations were more frequent in higher grade DCIS and closely resemble those previously detected in invasive breast cancer using the same technique. These data provide strong molecular support for the view that DCIS is a precursor lesion of invasive breast carcinoma.


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