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dc.contributor.authorHoyes, Katherine P
dc.contributor.authorLord, Brian I
dc.contributor.authorMcCann, Christine
dc.contributor.authorHendry, Jolyon H
dc.contributor.authorMorris, Ian D
dc.date.accessioned2009-11-06T16:46:47Z
dc.date.available2009-11-06T16:46:47Z
dc.date.issued2001-11
dc.identifier.citationTransgenerational effects of preconception paternal contamination with (55)Fe. 2001, 156 (5 Pt 1):488-94 Radiat. Res.en
dc.identifier.issn0033-7587
dc.identifier.pmid11604061
dc.identifier.urihttp://hdl.handle.net/10541/85614
dc.description.abstractThe conjecture that germline mutations induced by radiation exposure before conception may predispose subsequent offspring to cancer remains contentious. Previous experimental studies have shown that preconception paternal irradiation with (239)Pu induces perturbations in the hemopoietic systems of offspring and influences sensitivity to a secondary carcinogen. In the present study, male DBA2 mice were injected intravenously with the Auger electron emitter (55)Fe (4 kBq g(-1)) 18 or 84 days before mating with normal females. Comet analysis showed an increased incidence of DNA strand breaks in sperm from contaminated animals after 84 days, but not after 18 days, indicating spermatogonial rather than spermatid damage. Offspring were either assayed for changes in bone marrow stem cells and committed progenitors or challenged with the chemical carcinogen methyl nitrosourea (MNU, 50 mg/kg) at 10 weeks of age and monitored for the onset of malignancy. Offspring from irradiated fathers had normal peripheral blood profiles, although the stem cell population was amplified in offspring arising from those exposed to (55)Fe at 84 days before conception. Exposure to MNU significantly increased the incidence of lympho-hemopoietic malignancies in offspring from the 84-day group, but not in those from the 18-day group. These findings support the hypothesis that aberrations that are potentially leukemogenic may be transmitted to offspring after radiation damage to the paternal germline.
dc.language.isoenen
dc.subjectRadiation-Induced Leukaemiaen
dc.subject.meshAnimals
dc.subject.meshBlood Cell Count
dc.subject.meshDNA Damage
dc.subject.meshFetus
dc.subject.meshIron Radioisotopes
dc.subject.meshLeukemia, Radiation-Induced
dc.subject.meshMale
dc.subject.meshMethylnitrosourea
dc.subject.meshMice
dc.subject.meshMice, Inbred DBA
dc.subject.meshPaternal Exposure
dc.subject.meshSpermatozoa
dc.subject.meshTestis
dc.titleTransgenerational effects of preconception paternal contamination with (55)Fe.en
dc.typeArticleen
dc.contributor.departmentCancer Research Campaign Experimental Haematology, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, M20 4BX, United Kingdom.en
dc.identifier.journalRadiation Researchen
html.description.abstractThe conjecture that germline mutations induced by radiation exposure before conception may predispose subsequent offspring to cancer remains contentious. Previous experimental studies have shown that preconception paternal irradiation with (239)Pu induces perturbations in the hemopoietic systems of offspring and influences sensitivity to a secondary carcinogen. In the present study, male DBA2 mice were injected intravenously with the Auger electron emitter (55)Fe (4 kBq g(-1)) 18 or 84 days before mating with normal females. Comet analysis showed an increased incidence of DNA strand breaks in sperm from contaminated animals after 84 days, but not after 18 days, indicating spermatogonial rather than spermatid damage. Offspring were either assayed for changes in bone marrow stem cells and committed progenitors or challenged with the chemical carcinogen methyl nitrosourea (MNU, 50 mg/kg) at 10 weeks of age and monitored for the onset of malignancy. Offspring from irradiated fathers had normal peripheral blood profiles, although the stem cell population was amplified in offspring arising from those exposed to (55)Fe at 84 days before conception. Exposure to MNU significantly increased the incidence of lympho-hemopoietic malignancies in offspring from the 84-day group, but not in those from the 18-day group. These findings support the hypothesis that aberrations that are potentially leukemogenic may be transmitted to offspring after radiation damage to the paternal germline.


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