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p16基因启动子区域CpG岛的高甲基化作为高危组弥漫性大B细胞淋巴瘤的预后因素

Hypermethylation of CpG islands in p16 as a prognostic factor for diffuse large B-cell lymphoma in a high-risk group.

作者信息

Shiozawa Eisuke, Takimoto Masafumi, Makino Reiko, Adachi Daisuke, Saito Bungo, Yamochi-Onizuka Toshiko, Yamochi Tadanori, Shimozuma Junko, Maeda Takashi, Kohno Yohko, Kawakami Keiichiro, Nakamaki Tsuyoshi, Tomoyasu Shigeru, Shiokawa Akira, Ota Hidekazu

机构信息

Second Department of Pathology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-Ku, Tokyo 142-8555, Japan.

出版信息

Leuk Res. 2006 Jul;30(7):859-67. doi: 10.1016/j.leukres.2005.11.004. Epub 2006 Jan 9.

Abstract

PURPOSE

The aim of the study was to analyze the methylation status of the promoter regions of p15 and p16 and to assess the prognostic significance of promoter hypermethylation in diffuse large B-cell lymphoma (DLBCL).

EXPERIMENTAL DESIGN

DLBCL was diagnosed by morphology and immunohistochemical analysis according to the World Health Organization (WHO) classification. The methylation status of CpG islands in the p15 and p16 promoters was analyzed by methylation-specific polymerase chain reaction in 49 DLBCLs.

RESULTS

Hypermethylation of the p15 and p16 promoters was detected in 20 (41%) and 22 (45%) of the 49 DLBCLs, respectively. Among all patients with DLBCL, there was no significant difference in the overall survival between those with hypermethylated and unmethylated p15 (P=0.442) or between those with hypermethylated and unmethylated p16 (P=0.468). Therefore, methylation was analyzed in combination with evaluation of clinical features using the international prognostic index (IPI). In the high-intermediate-risk and high-risk groups, patients with hypermethylated p16 had significantly lower survival rates than those of patients in the same risk group with unmethylated p16 (P=0.010).

CONCLUSIONS

Our results suggest that hypermethylation of the p16 promoter indicates a poor prognosis in high-intermediate-risk and high-risk DLBCL patients, and may be a useful marker for selection of appropriate treatment when used in conjunction with the IPI.

摘要

目的

本研究旨在分析p15和p16启动子区域的甲基化状态,并评估启动子高甲基化在弥漫性大B细胞淋巴瘤(DLBCL)中的预后意义。

实验设计

根据世界卫生组织(WHO)分类,通过形态学和免疫组化分析诊断DLBCL。采用甲基化特异性聚合酶链反应分析49例DLBCL中p15和p16启动子中CpG岛的甲基化状态。

结果

49例DLBCL中,分别有20例(41%)和22例(45%)检测到p15和p16启动子高甲基化。在所有DLBCL患者中,p15启动子高甲基化和未甲基化患者的总生存率无显著差异(P=0.442),p16启动子高甲基化和未甲基化患者的总生存率也无显著差异(P=0.468)。因此,结合国际预后指数(IPI)对临床特征进行评估来分析甲基化情况。在高中危和高危组中,p16启动子高甲基化的患者生存率显著低于同风险组中p16未甲基化的患者(P=0.010)。

结论

我们的结果表明,p16启动子高甲基化表明高中危和高危DLBCL患者预后不良,与IPI联合使用时可能是选择合适治疗方法的有用标志物。

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