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人类卵巢癌中c-Ha-ras1基因座的等位基因缺失。

Allele loss at the c-Ha-ras1 locus in human ovarian cancer.

作者信息

Lee J H, Kavanagh J J, Wharton J T, Wildrick D M, Blick M

机构信息

Department of Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

Cancer Res. 1989 Mar 1;49(5):1220-2.

PMID:2917352
Abstract

Recent reports have shown allele loss at the c-Ha-ras1 locus on the short arm of chromosome 11 in some types of tumors. To determine whether loss of heterozygosity occurs at the c-Ha-ras1 locus in uncultured human ovarian carcinomas we used Southern blot analysis to study DNA from 17 pairs of ovarian tumors and matched white blood cell samples from the same patients. In one of these 17 tumors, the c-Ha-ras1 locus was rearranged, and in five tumor DNAs from ten informative patients, a c-Ha-ras1 allele was lost. This loss, of relatively high incidence, appears to be an important characteristic of human ovarian cancer and may provide a useful tool for understanding its biological behavior.

摘要

最近的报告显示,在某些类型的肿瘤中,11号染色体短臂上的c-Ha-ras1基因座存在等位基因缺失。为了确定未培养的人类卵巢癌中c-Ha-ras1基因座是否发生杂合性缺失,我们使用Southern印迹分析来研究17对卵巢肿瘤的DNA以及来自同一患者的匹配白细胞样本。在这17个肿瘤中的1个中,c-Ha-ras1基因座发生了重排,在来自10名信息丰富患者的5个肿瘤DNA中,一个c-Ha-ras1等位基因缺失。这种发生率相对较高的缺失似乎是人类卵巢癌的一个重要特征,可能为理解其生物学行为提供一个有用的工具。

相似文献

1
Allele loss at the c-Ha-ras1 locus in human ovarian cancer.人类卵巢癌中c-Ha-ras1基因座的等位基因缺失。
Cancer Res. 1989 Mar 1;49(5):1220-2.
2
Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas.人类卵巢癌中6号染色体长臂、11号和17号染色体上杂合性的频繁缺失。
Cancer Res. 1990 May 1;50(9):2724-8.
3
Allele loss from chromosome 17 in ovarian cancer.卵巢癌中17号染色体的等位基因缺失。
Oncogene. 1990 Oct;5(10):1581-3.
4
[Frequency and rearrangements of alleles of proto-oncogene c-Ha-ras-1 and their association with development of various malignant tumors in man].[原癌基因c-Ha-ras-1等位基因的频率、重排及其与人各种恶性肿瘤发生的关系]
Genetika. 1990 Mar;26(3):531-40.
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Allele loss on chromosome 11p is associated with poor survival in ovarian cancer.11号染色体短臂上的等位基因缺失与卵巢癌患者的不良生存率相关。
Dis Markers. 1992 Mar-Apr;10(2):95-9.
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Loss of the same alleles of HRAS1 and D11S151 in two independent pancreatic cancers from a patient with multiple endocrine neoplasia type 1.一名患有1型多发性内分泌腺瘤病患者的两个独立胰腺癌中HRAS1和D11S151的相同等位基因缺失。
Cancer Res. 1989 May 15;49(10):2716-21.
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Distribution and rearrangements of alleles of c-Ha-ras-1 protooncogene and their correlation with the development of lung, ovarian and thyroid cancers.c-Ha-ras-1原癌基因等位基因的分布与重排及其与肺癌、卵巢癌和甲状腺癌发生发展的相关性。
Neoplasma. 1990;37(6):647-55.
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Allele loss on chromosome 17 in ovarian cystic teratomas.卵巢囊性畸胎瘤中17号染色体上的等位基因缺失。
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Molecular genetic changes associated with ovarian cancer.与卵巢癌相关的分子遗传学改变。
Gynecol Oncol. 1994 Nov;55(2):245-52. doi: 10.1006/gyno.1994.1285.

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Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.人类BM88的克隆、表达及定位表明,它定位于11号染色体p15.5区域,该区域与贝克威思-维德曼综合征及肿瘤发生有关。
Biochem J. 2001 May 1;355(Pt 3):715-24. doi: 10.1042/bj3550715.
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Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.11号染色体p15.5区域170千碱基对区域的转录图谱:BWR1A基因的鉴定与突变分析揭示肿瘤样本中存在突变。
Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3873-8. doi: 10.1073/pnas.95.7.3873.
6
Monoallelic expression of the insulin-like growth factor-2 gene in ovarian cancer.胰岛素样生长因子-2基因在卵巢癌中的单等位基因表达。
Am J Pathol. 1996 Apr;148(4):1081-7.
7
Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer.人类卵巢癌中11号染色体q臂的杂合性缺失与扩增
Br J Cancer. 1993 Feb;67(2):268-73. doi: 10.1038/bjc.1993.51.
8
Alteration of the p53 tumor suppressor gene occurs independently of K-ras activation and more frequently in serous adenocarcinomas than in other common epithelial tumors of the human ovary.p53肿瘤抑制基因的改变独立于K-ras激活而发生,并且在浆液性腺癌中比在人类卵巢的其他常见上皮性肿瘤中更频繁出现。
Jpn J Cancer Res. 1994 Dec;85(12):1247-56. doi: 10.1111/j.1349-7006.1994.tb02937.x.
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