Kivi S, Mikelsaar A V
Hum Genet. 1980;56(1):111-4. doi: 10.1007/BF00281579.
To establish the significance of the Q- and C-band variants in risk for malignant disease, chromosome analysis was carried out in 37 women with carcinoma of the ovary or breast and in 40 controls. The frequencies of brilliant fluorescence in segments 3p11q11, 4p11q11, 13p11, 13p13, 14p11, 14p13, 15p11, 15p13, 21p11, 21p13, 22p11 and 22p13, the mean numbers of the brilliant fluorescent segments per cell per individual, and the frequency of inversions of the brilliant fluorescent centromeric area of chromosome 3 were established. The absolute and relative lengths of C bands in chromosomes 1,9, and 16 and the frequencies of C-band size heteromorphisms and inversions were determined. The results of the investigation indicate that the presence of Q and C variants is not associated with an elevated risk of ovarian and breast carcinoma.
为确定Q带和C带变异在恶性疾病风险中的意义,对37例卵巢癌或乳腺癌女性患者及40名对照者进行了染色体分析。确定了3p11q11、4p11q11、13p11、13p13、14p11、14p13、15p11、15p13、21p11、21p13、22p11和22p13节段中亮荧光的频率、每个个体每个细胞中亮荧光节段的平均数以及3号染色体亮荧光着丝粒区域的倒位频率。测定了1号、9号和16号染色体C带的绝对长度和相对长度以及C带大小异质性和倒位的频率。研究结果表明,Q带和C带变异的存在与卵巢癌和乳腺癌风险升高无关。