Fluorescence In Situ Hybridization법을 이용한 전립선암의 13번 및 17번 염색체의 관찰
Study on the Chromosome 13 and 17 of Prostatic Cancers by Fluorescence In Situ Hybridization Technique
박주영, 양채하,
소속 상세정보
박주영 ( )
경희대학교
양채하 ( )
경상대학교
KMID : 0358319960370080859
Abstract
To detect the numerical changes of the chromosome 13 and 17, containing tumor suppressor genes (retinoblastoma gene and p53) in normal tissue, intrapepithelial neoplasm and carcinoma of the prostate, the Fluorescence In Situ hybridization
technique
with
paraffin embedded tissue was done. Materials observed in this study consisted of the 14 caese of ocalized crcinoma (T2aN0M0) and 1 case of locally infiltrating cancer (T3aN2M0). The chromosoma mumber changes were counted at normal tissue,
intraepithelial neoplasm and neoplastic gland at the same radical prostatectomy specimen.
@ES The results were as follows:
@EN 1. There were no significant chromosomal number changes between 13 and 17 in each group.
2. The normal non-neoplastic duct, intraepithelial neoplasm and neoplastic gland of the experimental group showed no significant difference in chromosomal change.
3. There were significant changes more than 30% in chromosomal numbers between control Ychromosome and experimental chromosome 13 and 17 in each group.
4. With the results collected from this study, chromosomal aberration in number in prostate biopsy could represent the already established initiation of the cancerous change in prostate and the chromosomal aberration detection method would be a
good
early diagnostic modality to detect the high risk group who will develop the prostate cancer.
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