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Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma.

作者信息

van der Hout A H, Kok K, van den Berg A, Oosterhuis J W, Carritt B, Buys C H

机构信息

Department of Human Genetics, State University of Groningen, The Netherlands.

出版信息

Cancer Genet Cytogenet. 1988 Jun;32(2):281-5. doi: 10.1016/0165-4608(88)90292-0.

DOI:10.1016/0165-4608(88)90292-0
PMID:2835149
Abstract

Normal and tumorous nephrectomy specimens from seven renal cell carcinoma patients were subjected to a Southern analysis using chromosome #3-specific polymorphic probes. Three patients were not informative because of homozygosity at all loci studied. One patient showing heterozygosity at 3q in normal tissue had a tumor that remained heterozygous. In three patients the tumor showed loss of heterozygosity for a short arm market at 3p21. In one of them heterozygosity for a second short arm marker was also lost. Another of these three patients retained heterozygosity for this second short arm marker, as well as for a long arm marker, suggesting a chromosomal breakpoint between the loci for the two short arm markers. Our results demonstrate that the known involvement of a short arm region of chromosome #3 in the development of renal cell carcinoma can readily be further evaluated by direct molecular methods.

摘要

相似文献

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Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma.
Cancer Genet Cytogenet. 1988 Jun;32(2):281-5. doi: 10.1016/0165-4608(88)90292-0.
2
A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma.散发性肾细胞癌中3号染色体短臂的详细缺失图谱。
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Investigation of tumor suppressor genes apart from VHL on 3p by deletion mapping in sporadic clear cell renal cell carcinoma (cRCC).探讨散发性肾透明细胞癌(cRCC)中除 VHL 以外的 3p 缺失肿瘤抑制基因。
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PCR-based RFLP screening of the commonly deleted 3p loci in renal cortical neoplasms.基于聚合酶链反应的肾皮质肿瘤中常见缺失的3p位点的限制性片段长度多态性筛查。
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The use of molecular genetic analysis in the diagnosis of renal cell carcinoma.
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Papillary renal cell carcinoma. A morphologic and cytogenetic study of 11 cases.乳头状肾细胞癌。11例的形态学和细胞遗传学研究。
Am J Pathol. 1989 Jan;134(1):27-34.
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Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.冯·希佩尔-林道病、散发性小脑血管瘤病和肾细胞癌中两阶段突变模型的统计分析。
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Localization of the human HF.10 finger gene on a chromosome region (3p21-22) frequently deleted in human cancers.人类HF.10手指基因在人癌症中常发生缺失的一个染色体区域(3p21 - 22)上的定位。
Hum Genet. 1990 Apr;84(5):391-5. doi: 10.1007/BF00195806.
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