The LncRNA H19 rs217727 Polymorphism Is Associated with Oral Squamous Cell Carcinoma Susceptibility in Iranian Population

被引:13
作者
Ghapanchi, Jannan [1 ]
Ranjbar, Zahra [1 ]
Mokhtari, Mohammad Javad [2 ]
Koohpeima, Fatemeh [3 ]
Derakhshan, Maryam [3 ]
Khademi, Bijan [4 ]
Ghaderi, Hamid [5 ]
Sheikhbahaei, Shamsoddinali [6 ]
Aliabadi, Ehsan [7 ]
机构
[1] Shiraz Univ Med Sci, Sch Dent, Dept Oral Med, Shiraz, Iran
[2] Islamic Azad Univ, Dept Biol, Zarghan Branch, Young Researchers & Elite Club, Zarghan, Iran
[3] Shiraz Univ Med Sci, Sch Dent, Dept Operat Dent, Shiraz, Iran
[4] Shiraz Univ Med Sci, Sch Med, Shiraz Inst Canc Res, Canc Immunol Grp, Shiraz, Iran
[5] Imam Reza Clin, Shiraz, Iran
[6] Shiraz Univ Med Sci, Sch Dent, Student Res Comm, Shiraz, Iran
[7] Shiraz Univ Med Sci, Sch Dent, Dept Oral & Maxillofacial Surg, Shiraz, Iran
关键词
LONG NONCODING RNAS; H19; GENE; CANCER; RISK; SNPS;
D O I
10.1155/2020/1634252
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lack of protein-coding capacity is a main characteristic of long noncoding RNAs (lncRNAs) which, as molecular biomarkers, have found a novel pharmacological application in cancer and are reported to be important regulators of gene expression. H19 is reportedly involved in cancer progression and tumorigenesis. One of the most common types of head and neck cancers is oral squamous cell carcinoma (OSCC). The main objective of the present study was to evaluate the correlation of OSCC susceptibility with H19 gene in an Iranian population. This research was performed on 400 subjects of both sexes referred to the Namazi Hospital affiliated with the Shiraz University of Medical Sciences (SUMS). Individuals aged 15-88 years were divided into two groups: pathologically diagnosed patients with new-onset OSCC and healthy controls. After written and informed consent was obtained from the individuals, genomic DNA was extracted. The tetra-primer ARMS-PCR technique was performed for DNA genotyping by the use of specific primer pairs. The susceptibility of OSCC and H19 gene polymorphism sites was further analyzed (rs217727 and rs2107425). The allele and genotype frequencies of H19 rs2107425 polymorphism were similar between OSCC cases and controls. The H19 rs217727T allele frequency was significantly higher in OSCC cases (P=0.002), and the polymorphism of H19 rs217727 was associated with OSCC susceptibility in the codominant (OR=6.04, 95%CI=1.70-21.42, P=0.001 for TT genotype), dominant (OR=1.62, 95%CI=1.08-2.43, P=0.01), and recessive (OR=5.32, 95%CI=1.51-18.69, P=0.003) models. This study showed that rs217727 and OSCC susceptibility were statistically correlated in the Iranian population.
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页数:6
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