Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/3069
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dc.contributor.authorCuthbert, AP-
dc.contributor.authorBond, J-
dc.contributor.authorTrott, DA-
dc.contributor.authorGill, S-
dc.contributor.authorBroni, J-
dc.contributor.authorMarriott, A-
dc.contributor.authorKhoudoli, G-
dc.contributor.authorParkinson, EK-
dc.contributor.authorCooper, CS-
dc.contributor.authorNewbold, RF-
dc.coverage.spatial9en
dc.date.accessioned2009-03-04T15:07:57Z-
dc.date.available2009-03-04T15:07:57Z-
dc.date.issued1999-
dc.identifier.citationJournal of the National Cancer Institute. 91 (1) 37-45en
dc.identifier.issn0027-8874-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/3069-
dc.description.abstractBACKGROUND: Activation of the enzyme telomerase, which has been associated with cellular immortality, may constitute a key step in the development of human cancer. Telomerase is repressed in most normal human somatic cells. This study was conducted, using a genetic complementation approach, with the aim of identifying and mapping the genes responsible for repressing telomerase and, simultaneously, to establish the effect of experimentally induced telomerase repression on human tumor cell growth. METHODS: Individual human chromosomes isolated from normal diploid cells and tagged with bacterial antibiotic resistance genes (for later selection) were introduced into cells of the human breast carcinoma cell line 21NT by means of microcell transfer. Selected hybrid clones were screened for telomerase activity by use of the polymerase chain reaction-based telomere repeat amplification protocol (TRAP) assay, and the proliferative fate of the hybrid clones was determined. Regions of the introduced chromosomes associated with telomerase repression were mapped using segregant hybrids and a deletion analysis that employed microsatellite DNA markers. RESULTS: Strong repression of telomerase was observed following transfer of human chromosome 3 into 21NT cells but not after transfer of chromosomes 8, 12, or 20. The vast majority of hybrid clones with repressed telomerase entered permanent growth arrest after 10-18 population doublings. Deletion analysis of nonrepressed segregant monochromosome 3 hybrids indicated two regions on the short arm of chromosome 3 (3p21.3-p22 and 3p12-21.1) where telomerase regulator genes may be located. CONCLUSIONS: Telomerase in human breast cancer cells is efficiently repressed by a gene or genes on normal human chromosome 3p, and this repression is associated with permanent growth arrest of the tumor cells.en
dc.format.extent1139582 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoen-
dc.publisherOxford University Pressen
dc.subjectAdulten
dc.subjectBreast Neoplasms/*pathologyen
dc.subjectCell Division/drug effectsen
dc.subjectCell Fusionen
dc.subjectChromosomes/metabolism/ultrastructureen
dc.subjectChromosomes, Human, Pair 3/*geneticsen
dc.titleTelomerase repressor sequences on chromosome 3 and induction of permanent growth arrest in human breast cancer cellsen
dc.typeResearch Paperen
Appears in Collections:Biological Sciences
Dept of Life Sciences Research Papers

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