Dl. Mccormick et al., EXPOSURE TO 60 HZ MAGNETIC-FIELDS AND RISK OF LYMPHOMA IN PIM TRANSGENIC AND TSG-P53 (P53 KNOCKOUT) MICE, Carcinogenesis (New York. Print), 19(9), 1998, pp. 1649-1653
The results of a number of epidemiology studies suggest that exposure
to power frequency (50 and 60 Hz) magnetic fields may be a risk factor
for hematopoietic neoplasia, To generate experimental data to test th
is hypothesis, the influence of magnetic field exposure on lymphoma in
duction was determined in two strains of mice that are genetically pre
disposed to the disease, PIM mice, which carry the pim-1 oncogene, are
highly sensitive to lymphoma induction by N-ethyl-N-nitrosourea (ENU)
; ENU-treated PIM mice were studied as a 'high incidence' lymphoma mod
el, TSG-p53 (p53 knockout) mice, in which the p53 tumor suppressor gen
e has been deleted from the germ line, develop lymphoma as an age-rela
ted change; hemizygous TSG-p53 mice were studied as a 'low incidence'
lymphoma model, Beginning 1 day after a single i.p. injection of 25 mg
ENU/kg body wt, groups of 30 PIM mice/sex were exposed for 18.5 h/day
to pure, linearly polarized, transient-free 60 Hz magnetic fields at
field strengths of 0 (sham control), 0.02, 2.0 or 10.0 Gauss (G), An a
dditional group of 30 PIM mice/sex was exposed intermittently (1 h on,
1 h off) to 10.0 G fields, Groups of 30 TSG-p53 mice/sex were exposed
continuously to magnetic field strengths of 0 (sham control) or 10.0
G; TSG-p53 mice received no ENU, Studies were terminated after 23 week
s of magnetic held exposure. Lymphoma incidence in male PIM mice expos
ed continuously to 10.0 G magnetic fields was significantly reduced fr
om that seen in sex-matched sham controls; survival, lymphoma incidenc
e and lymphoma latency in other groups of PIM mice did not differ from
sham controls, Survival and lymphoma incidence in all groups of TSG-p
53 mice was 7% or less, regardless of magnetic field exposure regimen,
These data do not support the hypothesis that exposure to magnetic fi
elds is a significant risk factor for lymphoid neoplasia in mice with
a genetic predisposition to the disease.