Genetic variants of MUC4 are associated with susceptibility to and mortality of colorectal cancer and exhibit synergistic effects with LDL-C levels.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 25 11 2022
accepted: 13 06 2023
medline: 3 7 2023
pubmed: 29 6 2023
entrez: 29 6 2023
Statut: epublish

Résumé

As a disease with high mortality and prevalence rates worldwide, colorectal cancer (CRC) has been thoroughly investigated. Mucins are involved in the induction of CRC and the regulation of intestinal homeostasis but a member of the mucin gene family MUC4 has a controversial role in CRC. MUC4 has been associated with either decreased susceptibility to or a worse prognosis of CRC. In our study, the multifunctional aspects of MUC4 were elucidated by genetic polymorphism analysis in a case-control study of 420 controls and 464 CRC patients. MUC4 rs1104760 A>G polymorphism had a protective effect on CRC risk (AG, AOR = 0.537; GG, AOR = 0.297; dominant model, AOR = 0.493; recessive model, AOR = 0.382) and MUC4 rs2688513 A>G was associated with an increased mortality rate of CRC (5 years, GG, adjusted HR = 6.496; recessive model, adjusted HR = 5.848). In addition, MUC4 rs1104760 A>G showed a high probability of being a potential biomarker for CRC patients with low-density lipoprotein cholesterol (LDL-C) in the risk range while showing a significant synergistic effect with the LDL-C level. This is the first study to indicate a significant association between MUC4 genetic polymorphisms and CRC prevalence, suggesting a functional genetic variant with the LDL-C level, for CRC prevention.

Identifiants

pubmed: 37384668
doi: 10.1371/journal.pone.0287768
pii: PONE-D-22-32147
pmc: PMC10310026
doi:

Substances chimiques

Cholesterol, LDL 0
Mucins 0
MUC4 protein, human 0
Mucin-4 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0287768

Informations de copyright

Copyright: © 2023 Kwon et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Min Jung Kwon (MJ)

Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.

Jeong Yong Lee (JY)

Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.

Eo Jin Kim (EJ)

Division of Hematology/Oncology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Eun Ju Ko (EJ)

Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.

Chang Soo Ryu (CS)

Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.

Hye Jung Cho (HJ)

Department of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.

Hak Hoon Jun (HH)

Department of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.

Jong Woo Kim (JW)

Department of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.

Nam Keun Kim (NK)

Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.

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