Study of Human Leukocyte Antigen-G gene 14-bp Ins/Del and Codon 93 (CAC/CAT) Polymorphisms Association with Breast Cancer Susceptibility

被引:0
作者
Belkahla, Sana Taher [1 ]
Alkuwayti, Mayyadah Abdullah [2 ]
Amor, N. B. [3 ,4 ]
机构
[1] King Faisal Univ, Dept Basic Sci, Preparatory Year Deanship, Al Hasa 31982, Saudi Arabia
[2] King Faisal Univ, Coll Sci, Dept Biol Sci, Al Hasa 31982, Saudi Arabia
[3] King Faisal Univ, Vet Coll, Dept Publ Hlth, Al Hasa 31982, Saudi Arabia
[4] Univ Jendouba, Higher Inst Biotechnol Beja, Dept Biotechnol, Ave Habib Bourguiba, Beja 9000, Tunisia
关键词
Breast cancer; human leukocyte antigen-G codon 93 (CAC); 14-base pair insertion/deletion polymorphisms; amplification-refractory mutation system; polymerase chain reaction; SOLUBLE HLA-G; G EXPRESSION; CLASS-I; POOR-PROGNOSIS; COMPLEXITY; ESOPHAGEAL; SUBTYPES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Belkahla et al.: Study of Human Leukocyte Antigen-G gene 14-bp Ins/Del and Codon 93 (CAC/CAT) Human leukocyte antigen-G is a non-classic human leukocyte antigen I molecule. This protein is expressed aberrantly in numerous forms of malignant diseases like glioblastoma multiforme, ovarian cancer, lymphoblastic and breast cancer.Human leukocyte antigen-G polymorphisms association with breast cancer has been extensively studied. One amongst the foremost studied variants was human leukocyte antigen-G 14base pair insertion/deletion polymorphism. Nevertheless, results are contradictory or inconclusive. We aim to investigate two human leukocyte antigen-G polymorphisms, 14-base pair insertion/deletion 3' untranslated region and for the first time and codon 93 (CAC/CAT) polymorphisms potentially associated with breast cancer risk in the Tunisian population. This study involved 151 breast cancer patients and 187 healthy controls. Genotyping of the human leukocyte antigen-G codon 93 (CAC/CAT) and 14- base pair insertion/deletion variants was performed respectively by amplification-refractory mutation system and polymerase chain reaction. The analysis of genotype and allele frequencies revealed that human leukocyte antigen-G 14-base pair insertion/deletion polymorphism was associated with breast cancer susceptibility in the Tunisian population (Odds ratio=0.53, 95 % confidence interval=0.33-0.85, p=0.0022) without correlation with clinical parameters. We also observed an association of the human leukocyte antigen-G codon 93 (CAC/CAT) polymorphisms with breast cancer. In terms of analysis of the combined 14-base pair insertion/deletion and codon 93 CT genotype, we detected that the CC insertion/insertion and CC insertion/deletion genotype decrease the risk of breast cancer development (Odds ratio=0.2083; p=0.0097; Odds ratio=0.3571; p=0.0053, respectively). In addition, the haplotype frequency distribution analysis disclosed that the C insertion haplotype has a protective effect against breast cancer development (Odds ratio=0.4749; 95 % confidence interval=0.4425-0.9277; p=0.0153). Taken together, female's homozygosity for human leukocyte antigen-G 14-base pair insertion and human leukocyte antigen-G codon 93 (CAC) alleles may protect against breast cancer susceptibility.
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页码:90 / 97
页数:8
相关论文
共 49 条
[1]  
Al-Omar SY, 2019, GENET MOL RES, V18
[2]   Biology of HLA-G in cancer: a candidate molecule for therapeutic intervention? [J].
Amiot, Laurence ;
Ferrone, Soldano ;
Grosse-Wilde, Hans ;
Seliger, Barbara .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (03) :417-431
[3]   HLA-G Genotype/Expression/Disease Association Studies: Success, Hurdles, and Perspectives [J].
Amodio, Giada ;
Gregori, Silvia .
FRONTIERS IN IMMUNOLOGY, 2020, 11
[4]   Possible roles of HLA-G regulating immune cells in pregnancy and endometrial diseases via KIR2DL4 [J].
Bai, Yixuan ;
Liang, Junhui ;
Liu, Wei ;
Wang, Fei ;
Li, Changzhong .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2020, 142
[5]   Plasma soluble HLA-G is a potential biomarker for diagnosis of colorectal, gastric, esophageal and lung cancer [J].
Cao, M. ;
Yie, S. -M. ;
Liu, J. ;
Ye, S. R. ;
Xia, D. ;
Gao, E. .
TISSUE ANTIGENS, 2011, 78 (02) :120-128
[6]   Beyond the increasing complexity of the immunomodulatory HLA-G molecule [J].
Carosella, Edgardo D. ;
Favier, Benoit ;
Rouas-Freiss, Nathalie ;
Moreau, Philippe ;
LeMaoult, Joel .
BLOOD, 2008, 111 (10) :4862-4870
[7]   HLA-G: An Immune Checkpoint Molecule [J].
Carosella, Edgardo D. ;
Rouas-Freiss, Nathalie ;
Roux, Diana Tronik-Le ;
Moreau, Philippe ;
LeMaoult, Joel .
ADVANCES IN IMMUNOLOGY, VOL 127, 2015, 127 :33-144
[8]   In silico analysis of microRNAS targeting the HLA-G 3′ untranslated region alleles and haplotypes [J].
Castelli, Erick C. ;
Moreau, Philippe ;
Oya e Chiromatzo, Alynne ;
Mendes-Junior, Celso Teixeira ;
Veiga-Castelli, Luciana C. ;
Yaghi, Layale ;
Giuliatti, Silvana ;
Carosella, Edgardo D. ;
Donadi, Eduardo Antonio .
HUMAN IMMUNOLOGY, 2009, 70 (12) :1020-1025
[9]   NK cytolysis is dependent on the proportion of HLA-G expression [J].
Chen, Bao-Guo ;
Xu, Dan-Ping ;
Lin, Aifen ;
Yan, Wei-Hua .
HUMAN IMMUNOLOGY, 2013, 74 (03) :286-289
[10]   The 14 bp deletion polymorphisms in HLA-G gene play an important role in the expression of soluble HLA-G in plasma [J].
Chen, X. -Y. ;
Yan, W. -H. ;
Lin, A. ;
Xu, H. -H. ;
Zhang, J. -G. ;
Wang, X. -X. .
TISSUE ANTIGENS, 2008, 72 (04) :335-341