Imianitov E N, Chernitsa O I, Nikiforova I F, Serova O M, Sokolov S I, Laur O Iu, Togo A V, Kniazev P G
Mol Biol (Mosk). 1993 Jul-Aug;27(4):888-94.
Amplification of oncogenes erbb-2, erbb-1, c-myc and losses of heterozygosity (LOH) at chromosomes 11p (probe hras-1), 17p (probe ynz-22) and 17q (probe thh-59) were studied in 165 human tumours (60 breast, 22 ovary, 40 colorectal, 23 lung, and 20 thyroid carcinomas). The correlation (P < 0.01) between the increased copy number of mentioned oncogenes and LOH at 17p was demonstrated for tumours tested: extra copies of these oncogenes were revealed in 11 of 46 DNA specimens with LOH on ynz-22, but only in 3 of 61 without LOH. This correlation was mostly due to frequent combinations between erbb-2 amplification and 17p deletions; the incidence of increased copy number of erbb-1 and c-myc oncogenes was not high enough for final conclusions about the association of their alterations with LOH at chromosome 17p.
在165例人类肿瘤(60例乳腺癌、22例卵巢癌、40例结直肠癌、23例肺癌和20例甲状腺癌)中研究了癌基因erbb - 2、erbb - 1、c - myc的扩增以及11号染色体p臂(探针hras - 1)、17号染色体p臂(探针ynz - 22)和17号染色体q臂(探针thh - 59)的杂合性缺失(LOH)情况。对于所检测的肿瘤,上述癌基因拷贝数增加与17号染色体p臂LOH之间存在相关性(P < 0.01):在46例ynz - 22存在LOH的DNA样本中,有11例检测到这些癌基因的额外拷贝,但在61例无LOH的样本中仅3例检测到。这种相关性主要归因于erbb - 2扩增与17号染色体p臂缺失的频繁组合;erbb - 1和c - myc癌基因拷贝数增加的发生率不足以得出关于它们的改变与17号染色体p臂LOH之间关联的最终结论。