Maeda Kazuya, Kawakami Kazuyuki, Ishida Yoshinori, Ishiguro Kaname, Omura Kenji, Watanabe Go
Department of Surgery, Kanazawa University School of Medicine, 13-1 Takaramachi, Kanazawa, Ishikawa 920 8641, Japan.
Oncol Rep. 2003 Jul-Aug;10(4):935-8.
Promoter hypermethylation of the CDKN2A gene has been suspected to be involved in the carcinogenesis of colorectal cancers. However, the relations between CDKN2A hypermethylation and clinicopathological findings, and patient prognosis, remain inconclusive. We analyzed the CDKN2A methylation status in primary colorectal cancers using real-time methylation specific PCR (MethyLight) which enables quantitative measuring of the methylation level. CDKN2A promoter methylation was detectable in 55 (61.1%) of 90 tumor samples and the median level of the methylation was 0.187 (range 0.00-197.9). The methylation value of CDKN2A was correlated with certain clinicopathological findings, including tumor differentiation (p=0.018), and Dukes stage (p=0.016). In survival analysis, the CDKN2A methylation level was correlated with a poor prognosis of the patient with colorectal cancer for either all cases (p=0.014) or Dukes C (p=0.004) cases that were analyzed. These results suggest that CDKN2A methylation status is a prognostic factor in colorectal cancer and may be of use for the patient specific design of therapy.
CDKN2A基因启动子的高甲基化被怀疑与结直肠癌的致癌作用有关。然而,CDKN2A高甲基化与临床病理特征以及患者预后之间的关系仍无定论。我们使用实时甲基化特异性PCR(MethyLight)分析了原发性结直肠癌中CDKN2A的甲基化状态,该方法能够定量测量甲基化水平。在90个肿瘤样本中的55个(61.1%)中可检测到CDKN2A启动子甲基化,甲基化的中位水平为0.187(范围0.00 - 197.9)。CDKN2A的甲基化值与某些临床病理特征相关,包括肿瘤分化(p = 0.018)和Dukes分期(p = 0.016)。在生存分析中,无论是所有病例(p = 0.014)还是分析的Dukes C期(p = 0.004)病例,CDKN2A甲基化水平都与结直肠癌患者的不良预后相关。这些结果表明,CDKN2A甲基化状态是结直肠癌的一个预后因素,可能有助于针对患者的个性化治疗设计。