Uno Miyuki, Oba-Shinjo Sueli Mieko, de Aguiar Paulo Henrique, Leite Claudia C, Rosemberg Sérgio, Miura Flávio K, Junior Raul Marino, Scaff Milberto, Nagahashi Marie Suely Kazue
Department of Neurology, School of Medicine, University of São Paulo, Av. Dr Arnaldo 455, Cerqueira César, room 4110, 01246-903 São Paulo, SP, Brazil.
Cancer Lett. 2005 Jun 28;224(2):321-7. doi: 10.1016/j.canlet.2004.10.022. Epub 2004 Dec 7.
Alteration in TP53 is the most common genetic event reported for many tumors, including astrocytomas. The majority of studies, on analyzing TP53 mutations, have not included all splice junctions. Consequently, splice site mutations are thought to be relatively infrequent. TP53 were examined for mutations by polymerase chain reaction, single strand conformation polymorphism and direct sequencing in cases of diffuse astrocytomas. We found TP53 mutations in 17.8% (8 out of 45) of the tumors tested: 3 splicing, 3 missense and 2 silent mutations. We have shown that splice site mutations of TP53 are more frequent than previously reported. These findings emphasize the importance of thorough screening of TP53 mutations in gliomas.
TP53改变是许多肿瘤(包括星形细胞瘤)中报道的最常见的基因事件。大多数分析TP53突变的研究并未涵盖所有剪接位点。因此,剪接位点突变被认为相对少见。在弥漫性星形细胞瘤病例中,通过聚合酶链反应、单链构象多态性和直接测序检测TP53的突变情况。我们在45个检测的肿瘤中有17.8%(8个)发现了TP53突变:3个剪接突变、3个错义突变和2个沉默突变。我们已经表明,TP53的剪接位点突变比之前报道的更为常见。这些发现强调了在胶质瘤中全面筛查TP53突变的重要性。