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通过定量聚合酶链反应检测髓母细胞瘤中的p53基因表达

p53 gene expression in medulloblastoma by quantitative polymerase chain reaction.

作者信息

Loda M, Giangaspero F, Badiali M, Capodieci P, Pession A

机构信息

Department of Pathology, University of Bologna, Ospedale Bellaria, Italy.

出版信息

Diagn Mol Pathol. 1992 Mar;1(1):36-44. doi: 10.1097/00019606-199203000-00006.

Abstract

The frequent cytogenetic abnormality--isochromosome 17q [i(17)q]--observed in medulloblastomas (MB) may result in altered expression of the oncosuppressor gene p53 that is located on 17p. p53 expression was therefore evaluated in five MBs and in one MB cell line derived from one of these tumors. Expression levels of p53 utilizing serially diluted unfractionated RNA from tumors and the cell line were assessed both by dot-blot and by reverse transcription (RT) followed by the polymerase chain reaction (PCR). The quality of RNA, efficiency of reaction, and transcript quantitation were determined by simultaneous transcription and amplification of a similarly sized fragment of the alpha-tubulin gene. All MBs showed low levels of expression of p53 compared to those found in normal tissues. p53 messenger RNA (mRNA) was significantly increased (two- to threefold) in the MB cell line compared to its tumor of origin and to the other MBs. Immunoperoxidase studies performed with monoclonal antibodies to the p53 protein product showed focal nuclear expression in one of five of the original tumors while most cells grown in vitro and in the xenograft were positive.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在髓母细胞瘤(MB)中观察到的常见细胞遗传学异常——17号染色体等臂染色体[i(17)q]——可能导致位于17p上的抑癌基因p53表达改变。因此,对5例MB及其中1例肿瘤来源的MB细胞系进行了p53表达评估。利用肿瘤和细胞系中连续稀释的未分级RNA,通过斑点印迹法以及逆转录(RT)后接聚合酶链反应(PCR)来评估p53的表达水平。通过同时转录和扩增α-微管蛋白基因的类似大小片段来确定RNA质量、反应效率和转录本定量。与正常组织相比,所有MB均显示p53表达水平较低。与起源肿瘤及其他MB相比,MB细胞系中的p53信使核糖核酸(mRNA)显著增加(两到三倍)。用针对p53蛋白产物的单克隆抗体进行的免疫过氧化物酶研究显示,在5例原发肿瘤中有1例出现局灶性核表达,而大多数体外培养和异种移植中的细胞呈阳性。(摘要截短于250词)

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