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Unger, K. ; Wienberg, J.* ; Riches, A.* ; Hieber, L. ; Walch, A.K. ; Brown, A. ; O'Brien, P.C.* ; Briscoe, C.* ; Gray, L.* ; Rodriguez, E. ; Jackl, G. ; Knijnenburg, J.* ; Tallini, G.* ; Ferguson-Smith, M.* ; Zitzelsberger, H.

Novel gene rearrangements in transformed breast cells identified by high-resolution breakpoint analysis of chromosomal aberrations.

Endocr. Relat. Cancer 17, 87-98 (2010)
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Chromosomal copy number alterations and chromosomal rearrangements are frequent mutations in human cancer. Unlike copy number alterations, little is known about the role and occurrence of chromosomal rearrangements in breast cancer. This may be due to the fact that chromosome-based breakpoint analysis is widely restricted to cultured cells. In order to identify gene rearrangements in breast cancer we studied the chromosomal breakpoints in radiation-transformed epithelial breast cell lines using a high-resolution array-based approach using 1Mb BAC arrays. The breakpoints were further narrowed down by FISH with clones from the 32k BAC library. The analysis of the cell lines B42-11 and B42-16 revealed rearrangements of chromosomes 7, 8, 10 and 12. We identified the genes Has2, Grid1, Ret, Cpm, Tbx3, Tbx5, Tuba1a, Wnt1 and Arf3 within the breakpoint regions. Quantitative RT-PCR showed a deregulated expression of all of these candidate genes except for Tbx5 and Tbx3. This is the first study demonstrating gene rearrangements and their deregulated mRNA expression in radiation-transformed breast cells. Since the gene rearrangements occurred in the transformed and tumourigenic cell lines only it is likely that these were generated in conjunction with malignant transformation of the epithelial breast cells and therefore might reflect early molecular events in breast carcinogenesis. Initial studies indicate that these gene alterations are also found in sporadic breast cancers.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter comparative genomic hybridization; mammary epithelial-cells; array-CGH data; in-vitro; RET/PTC rearrangements; tyrosine kinase; cancer; hyaluronan; expression; tumors
Sprache englisch
Veröffentlichungsjahr 2010
Prepublished im Jahr 2009
HGF-Berichtsjahr 2009
ISSN (print) / ISBN 1351-0088
e-ISSN 1479-6821
Zeitschrift Endocrine-Related Cancer
Quellenangaben Band: 17, Heft: 1, Seiten: 87-98 Artikelnummer: , Supplement: ,
Verlag BioScientifica
Verlagsort Bristol
Begutachtungsstatus Peer reviewed
Institut(e) Translational Metabolic Oncology (IDC-TMO)
Institute of Pathology (PATH)
Institute of Radiation Biology (ISB)
Research Unit Analytical Pathology (AAP)
POF Topic(s) 30203 - Molecular Targets and Therapies
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
30202 - Environmental Health
30205 - Bioengineering and Digital Health
Forschungsfeld(er) Radiation Sciences
Enabling and Novel Technologies
PSP-Element(e) G-501000-001
G-500300-001
G-500200-001
G-500390-001
PubMed ID 19858224
DOI 10.1677/ERC-09-0065
Scopus ID 77449138120
Erfassungsdatum 2009-12-31
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