CDKN2A methylation in esophageal cancer: a meta-analysis

Chongchang Zhou, Jinyun Li and Qun Li _

PDF  |  HTML  |  How to cite

Oncotarget. 2017; 8:50071-50083. https://doi.org/10.18632/oncotarget.18412

Metrics: PDF 1670 views  |   HTML 3443 views  |   ?  


Chongchang Zhou1, Jinyun Li2 and Qun Li1

1Department of Otorhinolaryngology Head and Neck Surgery, Lihuili Hospital of Ningbo University, Ningbo 315040, Zhejiang, China

2Department of Medical Oncology, Affiliated Hospital of Ningbo University, Ningbo 315000, Zhejiang, China

Correspondence to:

Qun Li, email: [email protected]

Jinyun Li, email: [email protected]

Keywords: CDKN2A, methylation, diagnosis, esophageal cancer, carcinogenesis

Received: January 31, 2017    Accepted: May 08, 2017    Published: June 08, 2017


CDKN2A is a tumor suppressor gene and is frequently inactivated in human cancers by hypermethylation of its promoter. However, the role and diagnostic value of CDKN2A methylation in esophageal cancer (EC) remains controversial. Therefore, we performed a meta-analysis, including data from 42 articles (2656 ECs, 612 precancerous lesions, and 2367 controls). A significant increase in the frequency of CDKN2A methylation was identified during EC carcinogenesis: cancer vs. controls, odds ratio (OR) = 12.60 (95 % CI, 8.90–17.85); cancer vs. precancerous lesions, OR = 2.89 (95% CI, 2.20–3.79); and precancerous lesions vs. controls, OR = 7.38, 95% (CI, 4.31–12.66). CDKN2A promoter methylation was associated with EC tumor grade (OR = 1.79; 95% CI, 1.20–2.67) and clinical stage (OR = 2.56; 95% CI, 1.33–4.92). Additionally, the sensitivity, specificity, and area under the summary receiver operating characteristic curve (AUC) for diagnosis of EC based on CDKN2A methylation were 0.52 (95% CI, 0.44–0.59), 0.96 (95% CI, 0.93–0.98), and 0.83 (95% CI, 0.79–0.86), respectively. AUCs for blood and tissue sample subgroups were 0.90 and 0.82, respectively. Our findings indicate that CDKN2A methylation has a vital role in EC tumorigenesis and could be a biomarker for early diagnosis of EC.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 18412