Evidence map›Paper›PMID 39611998›Full record

ArticleDiscover oncology2024

Exon 1 methylation status of CDH13 is associated with decreased overall survival and distant metastasis in patients with postoperative colorectal cancer.

PengCheng Xiang, PengJu Li, Xiaoqi Yuan, Xiuhao Zhao, Zitian Xiao, Bingguan Chen, Kenwen Liu, Evelyne Bischof, Junyi Han

Abstract read
In one paragraph

Article in Discover oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

PengCheng XiangDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
PengJu LiDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
Xiaoqi YuanDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
Xiuhao ZhaoDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
Zitian XiaoDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
Bingguan ChenDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China.
Kenwen LiuDepartment of Gastrointestinal Surgery, Ji'an Central People's Hospital, Jian, 343000, Jiangxi, China.
Evelyne BischofDepartment of Oncology and State Key Laboratory of Systems Medicine for Cancer of Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 200127, China.
Junyi HanDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai, Shanghai, 200120, China. doctortonyhjy@tongji.edu.cn.

Funding

National Natural Science Foundation of China 82160515The Special Disease Project Foundation of Pudong New Area, Shanghai PWZzb2022-06
6 · The paper itself

Abstract

backgroundCadherin 13 (CDH13) is a member of the cadherin superfamily that exerts tumor-suppressive effects on cancers derived from epithelial cells. Although hypermethylation of CDH13 promoter has been reported in various cancers, its prognostic value for colorectal cancer (CRC) is still controversial. The methylation alterations of CDH13 within exon 1 have not yet been investigated.

methodsA total of 49 CRC patients were recruited for the prospective study. The methylation status of CpG sites was quantified by Bisulfite Amplicon Sequencing (BSAS) in malignant tissues and adjacent normal tissues. The primary endpoint of the study was overall survival (OS) after surgery. The relationship between methylation level with pathological stage and OS was also evaluated.

resultsCompared with adjacent normal tissues, the overall average methylation level within exon 1 was significantly increased in tumor tissues (p < 0.001). The association study showed that the hypermethylation status of the CpG1 site was non-significantly associated with the presence of distant metastasis (p = 0.032). Moreover, the hypermethylation of two CpG sites, including CpG1 (p = 0.003) and CpG5 (p = 0.032), was associated with worse OS in CRC. Co-hypermethylation of CpG1 and CpG5 sites was significantly associated with a worse clinical outcome (HR: 4.43 [95% CI 1.27-15.46]; p = 0.019) in multivariate Cox regression analysis.

conclusionThe methylation level of CDH13 exon 1 in CRC tissue was significantly higher than in adjacent normal tissues. Hypermethylation at the CpG1 site suggests a risk of distant metastasis in CRC. The hypermethylation of the CpG1 site and CpG5 site, including the co-hypermethylation of these two sites, may serve as a valuable prognostic biomarker.

Indexed as

CDH13 geneColorectal cancer (CRC)CpG siteMethylation

Identifiers

PMID39611998
PMCPMC11607350

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