Kivi S, Mikelsaar A V
Cancer Genet Cytogenet. 1987 Sep;28(1):77-85. doi: 10.1016/0165-4608(87)90355-4.
To establish the significance of the variability of human chromosome constitutive heterochromatin areas (C-band variants) in a risk of malignancy, C-banding pattern study has been performed in 33 female patients with ovarian or breast adenocarcinoma. The control group included 180 healthy women. The following characteristics of C-bands on chromosomes #1, #9, and #16 were studied: (a) size, (b) size heteromorphisms and (c) inversions, using quantitative and semiquantitative methods of analysis. Our data show no significant difference in the presence of C-band size and location variants in chromosomes #1, #9, and #16 between the patients with adenocarcinoma of the ovary or breast and healthy women. From that we conclude that there is no causal association between the presence of C-band variants on chromosomes #1, #9, and #16 and an elevated risk of ovarian and breast adenocarcinoma.
为确定人类染色体组成性异染色质区域(C带变异)的变异性在恶性肿瘤风险中的意义,对33例卵巢或乳腺腺癌女性患者进行了C带模式研究。对照组包括180名健康女性。使用定量和半定量分析方法研究了1号、9号和16号染色体上C带的以下特征:(a)大小,(b)大小异质性和(c)倒位。我们的数据显示,卵巢或乳腺腺癌患者与健康女性在1号、9号和16号染色体上C带大小和位置变异的存在方面没有显著差异。由此我们得出结论,1号、9号和16号染色体上C带变异的存在与卵巢和乳腺腺癌风险升高之间没有因果关系。