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CDKN2A(p16)启动子高甲基化影响年轻肺癌患者的预后。

CDKN2A (p16) promoter hypermethylation influences the outcome in young lung cancer patients.

作者信息

Bradly Dawn P, Gattuso Paolo, Pool Mark, Basu Sanjib, Liptay Michael, Bonomi Philip, Buckingham Lela

机构信息

Department of Pathology, Rush University Medical Center, Chicago, IL, USA.

出版信息

Diagn Mol Pathol. 2012 Dec;21(4):207-13. doi: 10.1097/PDM.0b013e31825554b2.

Abstract

PURPOSE

Non-small cell lung cancer (NSCLC) occurs most frequently in individuals older than 60 years of age. Currently, no biological indicators associated with NSCLC in younger patients (30 to 60 y) have been identified. To explore epigenetic influences, promoter methylation of selected tumor suppressor genes was analyzed in early-stage NSCLC patients ranging in age from 30 to 87 years at diagnosis.

EXPERIMENTAL DESIGN

The analysis was performed on formalin-fixed tumor tissue from 193 surgically treated NSCLC patients (127, older than 60 y; 66, 60 y and younger). Methylation was quantified in p16, MGMT, DAPK, RASSF1, CDH1, LET7-3-a, NORE1(RASSF5), and PTEN promoters by pyrosequencing. p16 protein expression was assessed by immunohistochemistry (IHC). Outcome, defined by time to recurrence and overall survival, was evaluated by Kaplan-Meier analysis.

RESULTS

Promoter methylation levels were generally higher in patients older than 60 years of age than in patients 60 years or younger at diagnosis. Of the genes tested, methylation levels of the p16 promoter showed age-related differences. Although p16 promoter methylation was significantly lower using cut-points of 50 years or younger and 40 years or younger (P=0.001 to 0.012, respectively), p16 protein expression increased with age. Patients 60 years or younger with p16 promoter hypermethylation had a significantly shortened time to recurrence (P=0.002) and a shortened survival time (P=0.011). No effect of p16 hypermethylation was seen in patients older than 60 years.

CONCLUSIONS

p16 promoter hypermethylation was associated with a worse outcome in patients with age at diagnosis of 60 years or younger, but was not associated with the outcome in the older than 60-year age group. Overall, these data support methylation-dependent and methylation-independent age-related regulation of p16 expression with differential effects on the outcome after surgical resection for early-stage NSCLC.

摘要

目的

非小细胞肺癌(NSCLC)最常发生于60岁以上的个体。目前,尚未发现与年轻患者(30至60岁)NSCLC相关的生物学指标。为探究表观遗传影响,对诊断时年龄在30至87岁的早期NSCLC患者中选定肿瘤抑制基因的启动子甲基化进行了分析。

实验设计

对193例接受手术治疗的NSCLC患者(127例年龄大于60岁;66例年龄60岁及以下)的福尔马林固定肿瘤组织进行分析。通过焦磷酸测序对p16、MGMT、DAPK、RASSF1、CDH1、LET7-3-a、NORE1(RASSF5)和PTEN启动子中的甲基化进行定量。通过免疫组织化学(IHC)评估p16蛋白表达。通过Kaplan-Meier分析评估以复发时间和总生存定义的结局。

结果

诊断时年龄大于60岁的患者启动子甲基化水平通常高于60岁及以下的患者。在所检测的基因中,p16启动子的甲基化水平显示出与年龄相关的差异。尽管使用50岁及以下和40岁及以下的切点时p16启动子甲基化显著更低(分别为P = 0.001至0.012),但p16蛋白表达随年龄增加。p16启动子高甲基化的60岁及以下患者复发时间显著缩短(P = 0.002)且生存时间缩短(P = 0.011)。在年龄大于60岁的患者中未观察到p16高甲基化的影响。

结论

p16启动子高甲基化与诊断时年龄为60岁及以下患者的较差结局相关,但与年龄大于60岁组的结局无关。总体而言这些数据支持p16表达的甲基化依赖性和甲基化非依赖性年龄相关调节对早期NSCLC手术切除后结局有不同影响。

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