Suppr超能文献

甲状腺乳头状癌及其严重程度中的长链非编码RNA多态性

Long non-coding RNA polymorphisms in papillary thyroid cancer and its severity.

作者信息

Maruei-Milan R, Heidari Z, Aryan A, Asadi-Tarani M, Salimi S

机构信息

Departments of Clinical Biochemistry, Zahedan University of Medical Sciences , Zahedan, Iran.

Department of Internal Medicine, Zahedan University of Medical Sciences , Zahedan, Iran.

出版信息

Br J Biomed Sci. 2021 Apr;78(2):58-62. doi: 10.1080/09674845.2020.1829853. Epub 2021 Jan 20.

Abstract

: Long non-coding RNAs are likely to have a role in the pathogenesis of many diseases, including cancer. We hypothesised an effect of certain single nucleotide polymorphisms (SNPs) in papillary thyroid cancer. : Genomic SNPs in rs11333048, rs4977574, rs1333040 and rs10757274 were determined in 134 papillary thyroid cancer patients and 155 age- and sex-matched controls. : None of the ANRIL SNPs were individually linked to papillary thyroid cancer. However, the AAAC haplotype (A from rs11333048, A from rs4977574, A from rs1333040 and C from rs10757274, respectively) showed a protective effect from papillary thyroid cancer whilst the CAAC and CAGT haplotypes were associated with cancer. The rs1333048 CC variant was more frequent in patients with larger tumour size (≥1 cm) in a recessive model (OR 3.4 [95%CI, 1.1-11], P = 0.035). The rs4977574 AC variant was associated with smaller tumour size in an over-dominant model (OR 0.4 [95%CI, 0.2-1.0], P = 0.041). SNPs in rs10757274 (AA: p = 0.045) and rs1333040 (CC: p = 0.019) are linked to a lower likelihood of III-IV cancer stages in dominant or codominant models. : Certain haplotypes of SNPs are associated with papillary thyroid cancer. ANRIL rs1333048 and rs4977574 variants were associated with larger and smaller tumour sizes, respectively. rs10757274 and rs1333040 variants might lead to lower III-IV cancer stages. These SNPs may be important in the diagnosis of this form of thyroid cancer.

摘要

长链非编码RNA可能在包括癌症在内的多种疾病的发病机制中发挥作用。我们推测某些单核苷酸多态性(SNP)在甲状腺乳头状癌中具有影响。在134例甲状腺乳头状癌患者和155例年龄及性别匹配的对照中测定了rs11333048、rs4977574、rs1333040和rs10757274的基因组SNP。没有一个ANRIL SNP与甲状腺乳头状癌单独相关。然而,AAAC单倍型(分别来自rs11333048的A、来自rs4977574的A、来自rs1333040的A和来自rs10757274的C)对甲状腺乳头状癌有保护作用,而CAAC和CAGT单倍型与癌症相关。在隐性模型中,rs1333048 CC变异在肿瘤较大(≥1 cm)的患者中更常见(比值比3.4 [95%可信区间,1.1 - 11],P = 0.035)。在共显性模型中,rs4977574 AC变异与较小的肿瘤大小相关(比值比0.4 [95%可信区间,0.2 - 1.0],P = 0.041)。rs10757274(AA:p = 0.045)和rs1333040(CC:p = 0.019)的SNP在显性或共显性模型中与III - IV期癌症的可能性较低相关。某些SNP单倍型与甲状腺乳头状癌相关。ANRIL rs1333048和rs4977574变异分别与较大和较小的肿瘤大小相关。rs10757274和rs1333040变异可能导致较低的III - IV期癌症。这些SNP在这种甲状腺癌的诊断中可能很重要。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验