M. Monteil et al., INCREASED ANEUPLOID FREQUENCY IN SPERMATOZOA FROM A HODGKINS-DISEASE PATIENT AFTER CHEMOTHERAPY AND RADIOTHERAPY, Cytogenetics and cell genetics, 76(3-4), 1997, pp. 134-138
The frequency of sperm aneuploidy was investigated by fluorescence in
situ hybridization (FISH) in a Hodgkin's disease patient shortly after
he had received chemotherapy and radiotherapy. Sperm karyotyping of t
he same patient had previously shown multiple structural abnormalities
in most spermatozoa immediately after radiotherapy (day 0), whereas m
ost spermatozoa collected 5 wk later (day 38) exhibited normal metapha
se divisions (Rousseaux et al., 1993). Variations in the frequency of
aneuploidy could not be detected by sperm karyotyping. Multicolor FISH
on interphase spermatozoa revealed an increase in the rate of disomy
for chromosomes 1, 6, 11, X, and Y at day 0 as well as at day 38. The
high frequency of 24,XY (nondisjunction at meiosis I) and 24,XX (nondi
sjunction at meiosis II) spermatozoa (8.46% and 1.64% at day 0, respec
tively) from the Hodgkin's disease patient suggests that both meiosis
I and II are affected and that the X chromosome is frequently involved
in such malsegregation events. The rate of 46,XY diploidy was also in
creased in the patient's sperm, up to 0.62% at day 0. While radiothera
py probably affected the postmeiotic cells (spermatids), the patient's
cancer and/or chemotherapy are the two major factors that could have
affected the dividing spermatogonia and/or spermatocytes, resulting in
high aneuploidy rates.