Tibiletti M G, Sessa F, Bernasconi B, Cerutti R, Broggi B, Furlan D, Acquati F, Bianchi M, Russo A, Capella C, Taramelli R
Department of Pathology, Ospedale di Circolo, Varese, Italy.
Clin Cancer Res. 2000 Apr;6(4):1422-31.
To assess whether early breast lesions are the precursors of invasive carcinomas, three classes of breast lesions, namely benign tumors (including fibroadenomas), putative premalignant lesions (including cases of atypical hyperplasia), and invasive carcinomas, were compared at the cytogenetic and molecular cytogenetic levels. Genetic relatedness was clearly demonstrated by the sharing of several anomalies, among which 6q deletions outnumbered all of the other alterations detected. Indeed, deletions of the long arm of chromosome 6, most likely occurring in epithelial cells, were present in 83.9% of benign breast tumors, 64% of putative premalignant lesions, and 77.4% of analyzable carcinomas. Furthermore, the interval between 6q24 and qter appeared to be the common region of deletion in all three classes of breast lesions, whereas the minimal common region of deletion was 6q27-qter. Interestingly, the latter region was reported previously to be deleted in benign ovarian tumors and recently found to harbor a gene (SEN6) that is important for SV40-mediated immortalization of human cells.
为评估早期乳腺病变是否为浸润性癌的前体,在细胞遗传学和分子细胞遗传学水平上比较了三类乳腺病变,即良性肿瘤(包括纤维腺瘤)、推定的癌前病变(包括非典型增生病例)和浸润性癌。通过几种异常情况的共享清楚地证明了遗传相关性,其中6q缺失的数量超过了检测到的所有其他改变。实际上,6号染色体长臂的缺失很可能发生在上皮细胞中,在83.9%的良性乳腺肿瘤、64%的推定癌前病变和77.4%的可分析癌中存在。此外,6q24和qter之间的区间似乎是所有三类乳腺病变中共同的缺失区域,而最小的共同缺失区域是6q27-qter。有趣的是,先前报道后一区域在良性卵巢肿瘤中缺失,最近发现该区域含有一个对SV40介导的人类细胞永生化很重要的基因(SEN6)。