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人类和鼠类骨肉瘤细胞中p53基因的失活

Inactivation of p53 gene in human and murine osteosarcoma cells.

作者信息

Chandar N, Billig B, McMaster J, Novak J

机构信息

Orthopaedic Research Laboratory, Allegheny-Singer Research Institute, Pittsburgh, Pennsylvania 15212.

出版信息

Br J Cancer. 1992 Feb;65(2):208-14. doi: 10.1038/bjc.1992.43.

Abstract

We examined structure and expression of the p53 and Rb genes in a C3HOS transplantable mouse model of osteosarcoma. The results were compared to analogous studies conducted with five human osteosarcoma cell lines. The p53 gene was found rearranged in the mouse tumour. The rearrangement mapped to the first intron region of the p53 gene and as a result, no p53 expression could be detected in C3HOS tumours. Using p53 genomic probes, we have detected the same rearrangement in the original radiation-induced tumour and the various clones that were isolated from it. Deletion and rearrangement of the p53 gene were also found in three out of five of the human osteosarcoma cell lines (MG-63, G-292, Saos-2). No p53 expression could be detected in these three cell lines. In the affected human osteosarcoma cell lines, the rearrangement involved the first intron region. In addition, the mouse tumor was analysed for structural and expression changes in the Rb and the c-myc genes. Normal expression of both genes were detected in the murine tumour. Only one (Saos-2) human osteosarcoma cell line exhibited gross structural alteration in the retinoblastoma gene. The results suggest that the inactivation of p53 may be an important step in the development of osteosarcomas, and that a rearrangement affecting the first intron is common in osteosarcomas.

摘要

我们在C3HOS骨肉瘤可移植小鼠模型中研究了p53和Rb基因的结构及表达情况。将结果与对五种人类骨肉瘤细胞系进行的类似研究进行了比较。发现小鼠肿瘤中的p53基因发生了重排。重排定位于p53基因的第一个内含子区域,因此在C3HOS肿瘤中检测不到p53表达。使用p53基因组探针,我们在原始辐射诱导肿瘤及其分离出的各种克隆中检测到了相同的重排。在五种人类骨肉瘤细胞系中的三种(MG-63、G-292、Saos-2)中也发现了p53基因的缺失和重排。在这三种细胞系中检测不到p53表达。在受影响的人类骨肉瘤细胞系中,重排涉及第一个内含子区域。此外,对小鼠肿瘤的Rb和c-myc基因的结构和表达变化进行了分析。在小鼠肿瘤中检测到这两个基因的正常表达。只有一种(Saos-2)人类骨肉瘤细胞系在视网膜母细胞瘤基因中表现出明显的结构改变。结果表明,p53的失活可能是骨肉瘤发生发展中的一个重要步骤,并且影响第一个内含子的重排在骨肉瘤中很常见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b189/1977714/dc071f68c1f9/brjcancer00066-0071-a.jpg

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