H. Matsuura et al., INTERPHASE CYTOGENETICS OF PROSTATE-CANCER - FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) ANALYSIS OF JAPANESE CASES, British Journal of Cancer, 74(11), 1996, pp. 1699-1704
No numerical aberration of chromosomes that might be specific for pros
tate cancer has so far been established. We used fluorescence in situ
hybridisation (FISH) with centromere-specific probes for chromosomes 7
, 8, 17, X and Y to establish the distribution of centromere copy numb
ers in frozen-stored or freshly prepared samples of benign prostate hy
pertrophy (BPH) and to detect numerical aberrations of these chromosom
es in 28 prostate cancers from Japanese men. There was no significant
difference in the data of centromere copy numbers between fresh and fr
ozen-stored tissue. The most common aberration in prostate cancers was
a gain of chromosome 8 (57%), with numerical aberration of chromosome
7 being the second most frequent anomaly (50%). Numerical aberration
of chromosome 7 is most significantly associated with a higher Gleason
score (GS) (P<0.005) or with lymph node metastasis (P<0.001). Numeric
al aberration of several chromosomes, including chromosomes 7 and/or 8
, was common in aggressive prostate cancers. Loss of chromosome Y was
detected in only 4% of cases. FISH analysis thus proved to be a useful
method for detecting numerical aberrations of individual chromosomes,
with application to touch preparations of frozen-stored tissue having
the advantage of exact sampling of cancer foci. The results suggest t
hat numerical aberration of chromosome 7 is associated with aggressive
tumour behaviour and poor prognosis of patients with prostate cancer.
The association between genetic change and chromosomal abnormality sh
ould be studied in detail.