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在人类癌症中,erbB-2(Her-2/neu)、erbB-1(HER-1)和c-myc癌基因的扩增常与17号染色体短臂缺失同时出现。

[Amplification of the erbb-2 (Her-2/NEU), erbb-1 (HER-1) and c-myc oncogenes is often combined with the deletion of the short arm of chromosome 17 in human carcinoma].

作者信息

Imianitov E N, Chernitsa O I, Nikiforova I F, Serova O M, Sokolov S I, Laur O Iu, Togo A V, Kniazev P G

出版信息

Mol Biol (Mosk). 1993 Jul-Aug;27(4):888-94.

PMID:8103188
Abstract

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.

摘要

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。

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