The aim of this study was to detect numerical chromosomal aberrations
that may be involved in the progression of cervical intraepithelial ne
oplasia (CIN) toward cervical carcinoma, Therefore, cervical lesions (
five CIN 1, seven CIN 2, six CIN 3, six invasive carcinomas, and six n
ormal samples) were studied by in situ hybridization (ISH) on serial 3
-mu m-thick paraffin tissue sections, using a panel of eight centromer
ic DNA probes for chromosomes 1, 3, 6, 7, 8, 11, 17, and X. An estimat
ion of the percentage of dysplastic epithelium with abnormal ISH signa
ls per nucleus was made. Chromosome aneusomy could be detected in all
persisting and high-grade CIN lesions and invasive carcinomas, In most
cases, when one of the chromosomes showed aneusomy then all studied c
hromosomes showed numerical changes, Interestingly, the abnormal ISH s
ignals were found only in a varying part of the morphologically dyspla
stic epithelium, the remainder showing no such changes, In aneuploid r
egions of the CIN 1 lesions the mean chromosome index for all chromoso
mes was 1.97 +/- 0.03 with a range of 1.92 to 2.00, The chromosome ind
ex ratios of chromosomes 1, 7, and X showed a significant positive cor
relation with CIN grade (r greater than or equal to 0.74; P less than
or equal to 0.006). It is concluded that chromosome aneusomy of chromo
somes 1, 7, and X may be involved in the progression of CIN lesions.