Idbaih Ahmed, Boisselier Blandine, Marie Yannick, El Hallani Soufiane, Sanson Marc, Crinière Emmanuelle, Rodero Mathieu, Carpentier Catherine, Paris Sophie, Laigle-Donadey Florence, Ducray François, Hoang-Xuan Khê, Delattre Jean-Yves
INSERM, Unité 711, Groupe hospitalier Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75013 Paris, France.
Cancer Genet Cytogenet. 2007 Sep;177(2):103-7. doi: 10.1016/j.cancergencyto.2007.06.010.
The functional single-nucleotide polymorphism (SNP) in codon 72 of TP53 has been shown to be both a risk factor and a prognostic biomarker in various cancers. Such results were also reported in brain tumors, notably in astrocytomas. This SNP has never been precisely investigated in oligodendroglial tumors. We retrospectively analyzed blood samples of 275 oligodendroglial tumor patients for the TP53 codon 72 polymorphism and compared them with a series of 144 healthy controls. Arg/Arg, Arg/Pro, and Pro/Pro genotypes were found in 54.2 versus 60.4%, 39.3 versus 34.0%, and 7.3 versus 5.6% of patients and controls, respectively. This suggests no association between oligodendroglial tumors and the SNP in codon 72 of TP53. Similarly, no correlation was found among the TP53 codon 72 polymorphism and prognosis, p53 expression, and chromosomes 1p and 19q status.
TP53基因第72密码子的功能性单核苷酸多态性(SNP)已被证明是多种癌症的危险因素和预后生物标志物。脑肿瘤中也报道了类似结果,尤其是在星形细胞瘤中。该SNP从未在少突胶质细胞瘤中得到精确研究。我们回顾性分析了275例少突胶质细胞瘤患者血液样本中的TP53第72密码子多态性,并与144例健康对照进行比较。患者和对照中Arg/Arg、Arg/Pro和Pro/Pro基因型的比例分别为54.2%对60.4%、39.3%对34.0%、7.3%对5.6%。这表明少突胶质细胞瘤与TP53第72密码子的SNP之间无关联。同样,未发现TP53第72密码子多态性与预后、p53表达以及染色体1p和19q状态之间存在相关性。