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11q23.1和11q25 - qter酵母人工染色体(YACs)在体内可抑制肿瘤生长。

11q23.1 and 11q25-qter YACs suppress tumour growth in vivo.

作者信息

Koreth J, Bakkenist C J, Larin Z, Hunt N C, James M R, McGee J O

机构信息

Nuffield Department of Pathology and Bacteriology, University of Oxford, The John Radcliffe Hospital, Headington, UK.

出版信息

Oncogene. 1999 Feb 4;18(5):1157-64. doi: 10.1038/sj.onc.1202372.

Abstract

Frequent allelic deletion at chromosome 11q22-q23.1 has been described in breast cancer and a number of other malignancies, suggesting putative tumour suppressor gene(s) within the approximately 8 Mb deleted region. In addition, we recently described another locus, at the 11q25-qter region, frequently deleted in breast cancer, suggesting additional tumour suppressor gene(s) in this approximately 2 Mb deleted region. An 11q YAC contig was accessed and three YACs, one containing the candidate gene ATM at 11q23.1, and two contiguous YACs (overlapping for approximately 400-600 kb) overlying most of the 11q25 deleted region, were retrofitted with a G418 resistance marker and transfected into murine A9 fibrosarcoma cells. Selected A9 transfectant clones (and control untransfected and 'irrelevant' alphoid YAC transfectant A9 clones) were assayed for in vivo tumorigenicity in athymic female Balb c-nu/nu mice. All the 11q YAC transfectant clones demonstrated significant tumour suppression compared to the control untransfected and 'irrelevant' YAC transfected A9 cells. These results define two discrete tumour suppressor loci on chromosome 11q by functional complementation, one to a approximately 1.2 Mb region on 11q23.1 (containing the ATM locus) and another to a approximately 400-600 kb subterminal region on 11q25-qter.

摘要

乳腺癌及其他多种恶性肿瘤中均有报道11号染色体q22 - q23.1区域频繁发生等位基因缺失,这表明在约8 Mb的缺失区域内存在假定的肿瘤抑制基因。此外,我们最近还描述了另一个位点,位于11q25 - qter区域,在乳腺癌中也经常缺失,这表明在这个约2 Mb的缺失区域内存在其他肿瘤抑制基因。获取了一个11q YAC重叠群,并对三个YAC进行改造,一个在11q23.1处包含候选基因ATM,另外两个相邻的YAC(重叠约400 - 600 kb)覆盖了11q25缺失区域的大部分,为其装上G418抗性标记后转染到小鼠A9纤维肉瘤细胞中。对筛选出的A9转染克隆(以及未转染的对照和“无关”的α卫星YAC转染A9克隆)在无胸腺雌性Balb c - nu/nu小鼠中进行体内致瘤性检测。与未转染的对照和“无关”YAC转染的A9细胞相比,所有11q YAC转染克隆均表现出显著的肿瘤抑制作用。这些结果通过功能互补确定了11号染色体q上两个离散的肿瘤抑制位点,一个位于11q23.1上约1.2 Mb的区域(包含ATM位点),另一个位于11q25 - qter上约400 - 600 kb的亚末端区域。

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