2021
DOI: 10.1515/hmbci-2020-0051
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Genetic variants and risk of thyroid cancer among Iranian patients

Abstract: The definition of an exclusive panel of genetic markers is of high importance to initially detect among this review population. Therefore, we gave a summary of each main genetic marker among Iranian patients with thyroid cancer for the first time which were classified based on their cellular function. Due to the results, a significant relationship was found between SNP in codons 194, 280, and 399 (XRCC1), Allele 3434Thr (XRCC7), GC or CC genotype 31, G/C (Survivin), 399G>A (XRCC1), Tru9I (vitamin D receptor… Show more

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Cited by 4 publications
(2 citation statements)
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“…A few studies demonstrate IL-18 gene polymorphism is a genetic risk factor for PTC [15,16]; however, the expression status and clinicopathological significance of IL-18 in PTC have not been explored to our knowledge. In the present study, we demonstrate that IL-18 expression was significantly upregulated in PTC tissues and closely associated with lymph node metastasis.…”
Section: Introductionmentioning
confidence: 99%
“…A few studies demonstrate IL-18 gene polymorphism is a genetic risk factor for PTC [15,16]; however, the expression status and clinicopathological significance of IL-18 in PTC have not been explored to our knowledge. In the present study, we demonstrate that IL-18 expression was significantly upregulated in PTC tissues and closely associated with lymph node metastasis.…”
Section: Introductionmentioning
confidence: 99%
“…Studies have shown that NHEJ gene polymorphisms are associated with susceptibility to a wide variety of cancers and disease progression. For instance, XRCC7 gene polymorphisms play an important role in prostate cancer [7], bladder cancer [8], liver cancer [9], thyroid cancer [10], and lung cancer [11]. The other gene polymorphisms such as XRCC4, XRCC5, XRCC6, and LIG4 SNPs are also associated with many different types of cancers [12][13][14][15].…”
Section: Introductionmentioning
confidence: 99%