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Impact of genomic stability on protein expression in endometrioid endometrial cancer

Lomnytska, M. I. (författare)
Karolinska Institutet
Becker, S. (författare)
Unit of Cancer Proteomics, Department of Oncology and Pathology, Karolinska Institute, Karolinska University Hospital, SE-17176 Stockholm, Sweden
Gemoll, T. (författare)
Unit of Cancer Proteomics, Department of Oncology and Pathology, Karolinska Institute, Karolinska University Hospital, SE-17176 Stockholm, Sweden
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Lundgren, C. (författare)
Department of Gynaecological Oncology, Radiumhemmet, Karolinska University Hospital, Solna, SE-17176 Stockholm, Sweden
Habermann, J. (författare)
Department of Surgery, University of Lübeck, D-23538 Lübeck, Germany
Olsson, A. (författare)
Department of Oncology and Pathology, Karolinska Institute, Karolinska University Hospital, SE-17176 Stockholm, Sweden
Bodin, I. (författare)
Department of Oncology and Pathology, Karolinska Institute, Karolinska University Hospital, SE-17176 Stockholm, Sweden
Engström, Ulla (författare)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Hellman, Ulf (författare)
Uppsala universitet,Ludwiginstitutet för cancerforskning
Hellman, K. (författare)
Karolinska Institutet
Hellström, A-C (författare)
Karolinska Institutet
Andersson, S. (författare)
Karolinska Institutet
Mints, M. (författare)
Department of Obstetrics and Gynaecology, Karolinska University Hospital, Solna, Karolinska Institute, SE-17176 Stockholm, Sweden
Auer, G. (författare)
Karolinska Institutet
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 (creator_code:org_t)
2012-03-13
2012
Engelska.
Ingår i: British Journal of Cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 106:7, s. 1297-1305
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Genomic stability is one of the crucial prognostic factors for patients with endometrioid endometrial cancer (EEC). The impact of genomic stability on the tumour tissue proteome of EEC is not yet well established.METHODS: Tissue lysates of EEC, squamous cervical cancer (SCC), normal endometrium and squamous cervical epithelium were subjected to two-dimensional (2D) gel electrophoresis and identification of proteins by MALDI TOF MS. Expression of selected proteins was analysed in independent samples by immunohistochemistry.RESULTS: Diploid and aneuploid genomically unstable EEC displayed similar patterns of protein expression. This was in contrast to diploid stable EEC, which displayed a protein expression profile similar to normal endometrium. Approximately 10% of the differentially expressed proteins in EEC were specific for this type of cancer with differential expression of other proteins observed in other types of malignancy (e.g., SCC). Selected proteins differentially expressed in 2D gels of EEC were further analysed in an EEC precursor lesion, that is, atypical hyperplasia of endometrium, and showed increased expression of CLIC1, EIF4A1 and PRDX6 and decreased expression of ENO1, ANXA4, EMD and Ku70.CONCLUSION: Protein expression in diploid and aneuploid genomically unstable EEC is different from the expression profile of proteins in diploid genomically stable EEC. We showed that changes in expression of proteins typical for EEC could already be detected in precursor lesions, that is, atypical hyperplasia of endometrium, highlighting their clinical potential for improving early diagnostics of EEC.

Nyckelord

endometrioid endometrial cancer
genomic stability
marker protein patterns
atypical endometrioid hyperplasia

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