Evidence map›Paper›PMID 38046481›Full record

ArticleCureus2023

The Relationship Between CTLA-4 (-318 C/T) Polymorphism and Urothelial Cancer Carcinogenesis in Japanese Patients.

Putri Damayanti, Sa Tin Myo Hlaing, Khine Zin Aung, Hiromasa Tsukino, Takuji Hinoura, Yoshiki Kuroda

Abstract read
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Putri DamayantiDepartment of Public Health, Faculty of Medicine, University of Miyazaki, Miyazaki, JPN.
Sa Tin Myo HlaingDepartment of Public Health, Faculty of Medicine, University of Miyazaki, Miyazaki, JPN.
Khine Zin AungDepartment of Public Health, Faculty of Medicine, University of Miyazaki, Miyazaki, JPN.
Hiromasa TsukinoDepartment of Urology, Junwakai Memorial Hospital, Miyazaki, JPN.
Takuji HinouraDepartment of Public Health, Faculty of Medicine, University of Miyazaki, Miyazaki, JPN.
Yoshiki KurodaDepartment of Public Health, Faculty of Medicine, University of Miyazaki, Miyazaki, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Urothelial cancer is one of the most common types of urinary system cancer and there are several factors that can influence its growth. One of the most prominent factors among these is genetics. The Cytotoxic T-Lymphocyte Antigen-4 (CTLA-4) gene is suspected to be a susceptibility gene in urothelial carcinoma. The aim of this study is to investigate polymorphism in the CTLA-4 gene (CTLA-4 -318 C/T) and whether it is associated with urothelial cancer. Methods The study population consisted of 253 cases and 272 controls. In this case-control study, DNA was extracted from peripheral blood cells, and the CTLA-4 -318C/T genotypes were detected using polymerase chain reaction-restriction fragment length polymorphism. Results C/T (adjusted OR (aOR) 3.37; 95%CI: 1.98-5.74) genotype, C/T + T/T (aOR 3.25; 95%CI: 1.96-5.39) genotype, and T allele (aOR 2.94 95%CI: 1.87-4.62) all indicated they are significant risk factors for urothelial cancer, with the effects of polymorphism being higher in the nonsmoker group than in the smoker group. Furthermore, the association between polymorphism and urothelial cancer carcinogenesis was similar among men and women. Conclusions This is the first study examining the association between CTLA-4 -318C/T polymorphism and urothelial carcinoma in Japanese patients. A significant association between CTLA-4 -318C/T polymorphism and urothelial cancer among Japanese patients was detected in this study. This supports the development of research on polymorphisms in urothelial cancer and is an important root of immunoreactions in cancer. We believe this study will be beneficial to clarify the relationship between CTLA-4 polymorphism and urothelial cancer.

Indexed as

-318 c/t polymorphismctla-4immunoregulatory moleculejapaneseurothelial cancer

Identifiers

PMID38046481
PMCPMC10689122

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