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Biological significance of promoter hypermethylation of p14/ARF gene: relationships to p53 mutational status in Tunisian population with colorectal carcinoma.

机译:p14 / ARF基因启动子高甲基化的生物学意义:与突尼斯大肠癌人群中p53突变状态的关系。

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One of the most important pathways which are frequently affected in colorectal cancer is p53/ (MDM2)/p14ARF pathway. We aim to determine the methylation pattern of p14/ARF in relation to mutation of p53. This correlation was studied to investigate whether their alterations could be considered as a predictor factor of prognosis in colorectal cancer and whether it can be useful in early-stage diagnosis. Statistical analyses show that p14/ARF hypermethylation was correlated with rectum location (p = 0.004), primary TNM stage (p = 0.016), and advanced Astler-Coller stage (p = 0.024). The RT-PCR that revel 31 % of patients did not express p14/ARF mRNA or at very low level. A high concordance between CpG hypermethylation and the low levels (p < 0.005) was shown. In addition, our analyses demonstrate that patients with mutation in the p53 gene have a lack of the protein expression (p < 0.005). This category with negative expression of p53 had a shorter survival rate (p < 0.005). On the one hand, MSP pattern of p14/ARF were correlated with a lack of p53 expression (p = 0.007). We found that p53/p14ARF pathway was frequently deregulated among our patients. In our study, we demonstrate that hypermethylation of p14/ARF occurs early during CRC tumorogenesis. However, we did not find correlation between p14/ARF and survival. These results suggest that p14/ARF methylation pattern may constitute a predictor factor of CRC in early stage but it could not be considered as a prognostic factor. On the other hand and because of the reversibility of the methylation mechanism, it may be appropriate to target the demethylation of p14/ARF to develop new drogues for CRC.
机译:结直肠癌中经常受到影响的最重要途径之一是p53 /(MDM2)/ p14ARF途径。我们旨在确定与p53突变相关的p14 / ARF甲基化模式。研究了这种相关性,以研究它们的改变是否可被视为大肠癌预后的预测因素,以及它是否可用于早期诊断。统计分析表明p14 / ARF甲基化与直肠位置(p = 0.004),主要TNM分期(p = 0.016)和晚期Astler-Coller分期(p = 0.024)相关。反映31%患者的RT-PCR不表达p14 / ARF mRNA或表达水平很低。 CpG高甲基化与低水平之间存在高度一致性(p <0.005)。此外,我们的分析表明,p53基因突变的患者缺乏蛋白质表达(p <0.005)。 p53阴性表达的这类患者的生存期较短(p <0.005)。一方面,p14 / ARF的MSP模式与p53表达的缺乏相关(p = 0.007)。我们发现p53 / p14ARF通路在我们的患者中经常被放松。在我们的研究中,我们证明p14 / ARF的超甲基化发生在CRC肿瘤发生的早期。但是,我们未发现p14 / ARF与生存率之间存在相关性。这些结果表明,p14 / ARF甲基化模式可能构成了CRC的早期预测因素,但不能认为是预后因素。另一方面,由于甲基化机制的可逆性,以p14 / ARF的去甲基化为靶点开发CRC新的锥虫可能是适当的。

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