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The Variations' in Genes Encoding TIM-3 and Its Ligand, Galectin-9, Influence on ccRCC Risk and Prognosis
被引:4
作者:
Andrzejczak, Anna
[1
]
Tupikowski, Krzysztof
[2
]
Tomkiewicz, Anna
[1
]
Malkiewicz, Bartosz
[3
]
Ptaszkowski, Kuba
[4
]
Domin, Aleksandra
[1
]
Szydelko, Tomasz
[3
]
Karabon, Lidia
[1
]
机构:
[1] Polish Acad Sci, Hirszfeld Inst Immunol & Expt Therapy, Dept Expt Therapy, Lab Genet & Epigenet Human Dis, PL-53114 Wroclaw, Poland
[2] Lower Silesian Ctr Oncol Pulmonol & Hematol, Subdiv Urol, PL-53413 Wroclaw, Poland
[3] Wroclaw Med Univ, Univ Ctr Excellence Urol, Dept Minimally Invas & Robot Urol, PL-50556 Wroclaw, Poland
[4] Wroclaw Med Univ, Dept Clin Biomech & Physiotherapy Motor Syst Disor, PL-50556 Wroclaw, Poland
关键词:
TIM-3;
HAVCR2;
galectin-9 (LGALS9);
clear cell renal cell carcinoma (ccRCC);
single-nucleotide gene polymorphism (SNP);
immunological checkpoint;
disease risk;
overall survival;
T-CELL IMMUNOGLOBULIN;
EXPRESSION;
POLYMORPHISMS;
SUSCEPTIBILITY;
DISEASE;
CANCER;
DISEQUILIBRIUM;
ASSOCIATION;
VARIANTS;
SURVIVAL;
D O I:
10.3390/ijms24032042
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Renal cell cancer is the most common type of kidney cancer in adults, and clear cell renal cell carcinoma (ccRCC) is the most diagnosed type. T cell immunoglobulin and mucin-domain-containing-3 (TIM-3) belongs to immunological checkpoints that are key regulators of the immune response. One of the known TIM-3 ligands is galectin-9 (LGALS9). A limited number of studies have shown an association between TIM-3 polymorphisms and cancer risk in the Asian population; however, there is no study on the role of LGALS9 polymorphisms in cancer. The present study aimed to analyze the influence of TIM-3 and LGALS9 polymorphisms on susceptibility to ccRCC and patient overall survival (OS), with over ten years of observations. Using TaqMan probes, ARMS-PCR, and RFPL-PCR, we genotyped two TIM-3 single-nucleotide polymorphisms (SNPs): rs1036199 and rs10057302, and four LGALS9 SNPs: rs361497, rs3751093, rs4239242, and rs4794976. We found that the presence of the rs10057302 A allele (AC + AA genotypes) as well as the rs4794976 T allele (GT + TT genotypes) decreased susceptibility to ccRCC by two-fold compared to corresponding homozygotes. A subgroup analysis showed the association of some SNPs with clinical features. Moreover, TIM-3 rs1036199 significantly influenced OS. Our results indicate that variations within TIM-3 and LGALS9 genes are associated with ccRCC risk and OS.
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页数:18
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