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原发性脑恶性淋巴瘤:频繁的p16和p15基因缺失的证明

Primary malignant lymphoma of the brain: demonstration of frequent p16 and p15 gene deletions.

作者信息

Kumanishi T, Zhang S, Ichikawa T, Endo S, Washiyama K

机构信息

Department of Molecular Neuropathology, Niigata University.

出版信息

Jpn J Cancer Res. 1996 Jul;87(7):691-5. doi: 10.1111/j.1349-7006.1996.tb00279.x.

Abstract

The p16 (MTS-1) gene, a candidate tumor suppressor gene, was examined by means of Southern blot, PCR-SSCP (polymerase chain reaction-single-strand conformation polymorphism) and nucleotide analyses in 5 cases of primary malignant lymphoma of the brain. By Southern blot analysis, the p16 gene was found to be deleted in at least 4 cases, homozygously (3 cases) or hemizygously (1 case). The p15 (MTS-2) gene, another candidate tumor suppressor gene located in the vicinity of the p16 gene, to which it shows structural and functional similarity, was also found to be deleted in 4 cases. Our frequent detection (80%) of p16 and p15 gene deletions might suggest that these deletions are closely related to carcinogenesis in primary malignant lymphoma of the brain. SSCP and nucleotide analyses revealed no mutations of the p16 gene in any of the cases.

摘要

通过Southern印迹法、聚合酶链反应-单链构象多态性(PCR-SSCP)及核苷酸分析,对5例原发性脑恶性淋巴瘤患者的候选抑癌基因p16(MTS-1)进行了检测。通过Southern印迹分析发现,至少4例患者的p16基因发生缺失,其中纯合缺失3例,半合子缺失1例。另一个位于p16基因附近、与之具有结构和功能相似性的候选抑癌基因p15(MTS-2),也在4例患者中被发现有缺失。我们频繁检测到p16和p15基因缺失(80%),这可能表明这些缺失与原发性脑恶性淋巴瘤的致癌作用密切相关。SSCP和核苷酸分析显示,所有病例中p16基因均未发生突变。

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