Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.advisorRiches, Andrew Clive
dc.contributor.advisorBryant, Peter Edward
dc.contributor.advisorMill, Andrew
dc.contributor.authorMercer, John
dc.coverage.spatial266 p.en_US
dc.date.accessioned2016-10-06T09:33:13Z
dc.date.available2016-10-06T09:33:13Z
dc.date.issued1999
dc.identifier.urihttp://hdl.handle.net/10023/9613
dc.description.abstractThe human thyroid epithelial cell HTori-3 has been transformed with doses of either chronic and acute x-rays or strontium beta particles. Models of the past have relied upon animal cell systems to mimic in vitro carcinogenesis. The HTori-3 system hoped to overcome the limitations associated with these types of models by using a human thyroid cell line immortalised with the SV40 virus. HTori-3 human thyroid epithelial cells were irradiated in vitro, passaged and then transplanted into nude mice. Tumours that grew over a 2-6 month period were excised and re-established in culture. Samples were stored and all tumours were taken for histological examination. Chromosome spreads confirmed the human nature of all tumours. Following exposure to acute x-rays in the range of 0.25-2.0 Gy 13 tumours were observed in 25 recipients. Following 0.25-2.0 Gy of chronic x-rays 10 tumours from 25 recipients were observed. From a single 2 Gy exposure of strontium beta particles 3 primary tumours from 5 recipients were observed. The largest of these was re-transplanted in nude mice resulting in 100% incidence. All tumours were classified as undifferentiated anaplastic carcinomas. A small number of tumours were observed in the control cell lines, these may be the result of a general instability found with the partial transformed parental cell line. All 2Gy tumours and those previously established from this laboratory after alpha or gamma radiation were used to test for the presence of the delayed lethal death phenotype. A number of cell and molecular endpoints were used. These included plating efficiency, cell adherence, micronucleus formation and p53 status. In all incidences, the reproductive viability of irradiated cells was below that of non- irradiated cells at up to 4 weeks post-irradiation. The HTori-3 cell line and the techniques used to study the delayed effects of radiation may be applicable to other cell systems and may be a useful model to study the long-term effects of radiation induced genomic instability.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subject.lccQH465.R3M4
dc.subject.lcshRadiation carcinogenesisen_US
dc.subject.lcshDNA damageen_US
dc.subject.lcshEpithelial cellsen_US
dc.titleRadiation carcinogenesis and delayed lethal damage in a human thyroid epithelial cell lineen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


This item appears in the following Collection(s)

Show simple item record