Analysis of HLA-G 14 bp Insertion/Deletion Polymorphism and HLA-G, ILT2 and ILT4 Expression in Head and Neck Squamous Cell Carcinoma Patients

被引:1
|
作者
Durmanova, Vladimira [1 ]
Tedla, Miroslav [2 ]
Rada, Dusan [2 ]
Bandzuchova, Helena [3 ]
Kuba, Daniel [3 ]
Suchankova, Magda [1 ]
Ocenasova, Agata [1 ]
Bucova, Maria [1 ]
机构
[1] Comenius Univ, Inst Immunol, Fac Med, Bratislava 81108, Slovakia
[2] Comenius Univ, Univ Hosp Bratislava, Fac Med, Dept Ears Nose & Throat & Head & Neck Surg, Bratislava 85107, Slovakia
[3] Natl Transplant Org, Bratislava 83101, Slovakia
关键词
HLA-G; ILT receptor; head and neck squamous cell carcinoma; mRNA expression; real-time PCR; LEUKOCYTE ANTIGEN-G; INHIBITORY RECEPTOR; CANCER; PROGRESSION; MEDIATORS; LIGAND; GENE;
D O I
10.3390/diseases12020034
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
HLA-G is the checkpoint molecule involved in the suppression of the immune response. Increased expression of HLA-G and its ILTs receptors have been correlated with tumor progression in various cancer types. In head and neck squamous cell carcinoma (HNSCC) tumors, the effect of HLA-G, ILT2 and ILT4 expression on cancer development has to be explained. The 34 HNSCC patients and 98 controls were genotyped for the HLA-G 14 bp ins/del polymorphism. In HNSCC lesions, HLA-G, ILT2 and ILT4 mRNA expression was analysed using real-time PCR. The association between HLA-G, ILT2 and ILT4 mRNA expression and clinical variables (age at onset, TNM staging system and p16 positivity) was also evaluated. No genetic association between the HLA-G 14 bp ins/del and HNSCC risk was detected (p > 0.05). However, in the non-metastatic HNSCC group, a significantly higher HLA-G mRNA expression was noted in tumors in the T4 stage compared to those in the T1 and T2 stages (p = 0.0289). ILT2 mRNA expression was significantly increased in non-metastatic vs. metastatic tumors (p = 0.0269). Furthermore, a significantly higher ILT4 mRNA expression was noted in tumors in the T1+T2 stage compared to those in the T3 stage (p = 0.0495). Our results suggest that the HLA-G molecule creates an immunological microenvironment involved in HNSCC development.
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页数:14
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