Evidence map›Paper›PMID 36277013›Full record

ArticleComputational and mathematical methods in medicine2022

Association between ERCC1 Gene Polymorphism (rs11615) and Colorectal Cancer Susceptibility: A Meta-Analysis of Medical Image Fusion and Safety Applications.

Min Liu, Zhifeng Qiu, Qi Yang

Abstract read
In one paragraph

Article in Computational and mathematical methods in medicine, 2022. 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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5 · Who and what money

Authors and funding

3 authors.

Min LiuDepartment of Reproductive Medicine, First Affiliated Hospital, School of Medicine, Shihezi University, Shihezi, Xinjiang, China.ORCID https://orcid.org/0000-0002-1721-019X
Zhifeng QiuGenetic Laboratory, Maternal and Child Health Care Hospital of Baiyun District, Guangzhou, Guangdong 510010, China.
Qi YangClinical Laboratory, First Affiliated Hospital, School of Medicine, Shihezi University, Shihezi, Xinjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a malignant tumor of the colorectal mucosa epithelial tissue transformed. The fusion of data for medical imaging has become a central issue in such biomedical applications as image-guided surgery and radiotherapy. Currently, CRC has been one of the most threatening tumors affecting people's health worldwide. The excision repair cross-complementation group 1 (ERCC1) is a key enzyme for nucleotide excision repair (NER). Emerging epidemiological studies have indicated that the presence of colorectal cancer (CRC) may be relevant to the ERCC1 rs11615 genetic polymorphism. However, the results of ERCC1 rs11615 on CRC in these studies are controversial. We searched PubMed, Web of Science, Embase, CNKI, and CBM databases for the effects of ERCC1 rs11615 variant on CRC development. There was no meta-analysis focused on the diagnosis of colorectal cancer with ERCC1 rs11615 variant. We creatively carried out a meta-analysis of nine case-control studies and used Stata (version 12.0) software to integrate the pooled odds ratios (ORs) corresponding to a 95% confidence interval (CI) of overall and subgroup analysis. Our results suggest that a significant correlation was observed between rs11615 and the susceptibility of CRC OR 95% CI = 1.13 (1.04-1.23) under an allele genetic model and OR 95% CI = 1.14 (1.01-1.30) under a dominant genetic model for overall CRC. Significant statistical difference was also noted in Asians rather than Caucasians based on the ethnicity subgroups. These results suggested that there is a certain association between rs11615 and the susceptibility of colorectal cancer in the Asian populations.

Indexed as

Colorectal NeoplasmsEndonucleasesDNA-Binding ProteinsDNA RepairGenetic Predisposition to DiseaseHumansPolymorphism, GeneticPolymorphism, Single NucleotideRisk FactorsDNA-Binding ProteinsEndonucleasesERCC1 protein, human

Identifiers

PMID36277013
PMCPMC9586779

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