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结直肠癌中肿瘤 p16INK4 基因表达与预后的关系。

Tumor p16INK4 gene expression and prognosis in colorectal cancer.

机构信息

Department of Gastroenterological Surgery, Ishikawa Prefectural Central Hospital, Kanazawa, Ishikawa 920‑8530, Japan.

Department of General and Cardiothoracic Surgery, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Ishikawa 920‑0934, Japan.

出版信息

Oncol Rep. 2019 Feb;41(2):1367-1376. doi: 10.3892/or.2018.6884. Epub 2018 Nov 26.

Abstract

Hypermethylation of the tumor suppressor gene p16INK4 (p16) promoter is associated with worse prognosis in colorectal cancer (CRC). In the present study, it was investigated whether p16 mRNA expression correlates with the methylation of its promoter, and whether it influences prognosis in patients with CRC. DNA and RNA were extracted from 101 resected tumor specimens. A MethyLight assay was used to quantify p16 methylation in terms of percentage of methylated reference (PMR), and the expression of p16 mRNA was measured using reverse transcription‑polymerase chain reaction. Associations between p16 methylation or mRNA expression and patient survival were evaluated using Kaplan‑Meier analysis and Cox proportional hazards regression. p16 methylation was detected in 67 cases (66.3%) and the median PMR value was 0.344 (range, 0.00‑468.6). Using a cut‑off PMR value of 4, high p16 methylation was observed in 18 cases (17.8%). No significant association was observed between p16 methylation level and patient prognosis. As expected, a significant inverse association was observed between p16 methylation and mRNA expression (P=0.034). Amongst the 83 cases with low p16 methylation, a significantly worse outcome was identified in patients expressing high p16 mRNA expression levels (P=0.026). Multivariate analysis identified that p16 mRNA expression was an independent prognostic factor for worse survival (P=0.011). These results suggested a paradoxical association between high levels of p16 mRNA expression in the tumor and worse prognosis in patients with CRC.

摘要

肿瘤抑制基因 p16INK4(p16)启动子的高甲基化与结直肠癌(CRC)的预后不良相关。在本研究中,研究了 p16 基因启动子的甲基化是否与 p16 mRNA 表达相关,以及 p16 mRNA 表达是否影响 CRC 患者的预后。从 101 个切除的肿瘤标本中提取 DNA 和 RNA。使用 MethyLight 测定法根据甲基化参考百分比(PMR)定量测定 p16 甲基化,使用逆转录-聚合酶链反应测量 p16 mRNA 的表达。使用 Kaplan-Meier 分析和 Cox 比例风险回归评估 p16 甲基化或 mRNA 表达与患者生存之间的关联。在 67 例(66.3%)中检测到 p16 甲基化,中位数 PMR 值为 0.344(范围,0.00-468.6)。使用 4 的 PMR 截断值,观察到 18 例(17.8%)高 p16 甲基化。p16 甲基化水平与患者预后之间未观察到显著相关性。如预期的那样,p16 甲基化与 mRNA 表达之间存在显著的负相关(P=0.034)。在 83 例低 p16 甲基化的病例中,高 p16 mRNA 表达水平的患者预后明显较差(P=0.026)。多变量分析确定 p16 mRNA 表达是生存预后不良的独立预后因素(P=0.011)。这些结果表明,在结直肠癌患者中,肿瘤中 p16 mRNA 表达水平高与预后不良之间存在矛盾关联。

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