吉林大学学报(医学版) ›› 2013, Vol. 39 ›› Issue (2): 322-325.doi: 10.7694/jldxyxb20130229

• 基础研究 • 上一篇    下一篇

RET基因多态性与甲状腺乳头状癌的关联性分析

王 崇1, 刘晓莉2,史杰萍1,吴燕华1,王诗镔1 , 于雅琴1, 孙 辉2    

  1. 1. 吉林大学公共卫生学院流行病与卫生统计学教研室,吉林 长春 130021;2. 吉
    林大学中日联谊医院甲状腺外科,吉林 长春 130033
  • 收稿日期:2012-12-12 出版日期:2013-03-28 发布日期:2013-03-28
  • 通讯作者: 于雅琴(Tel: 0431-85619437,E-mail:yuyaqin5540@163.com);  孙 辉(Tel: 0431-89876655,E-mail:sunhui1229@163.com) E-mail:yuyaqin5540@163.com
  • 作者简介:王 崇(1986-),女,吉林省辉南县人,在读医学硕士,主要从事分子遗 传流行病学研究。 
  • 基金资助:

     吉林省科技厅自然科学基金资助课题(201015176)

Association analysis between RET gene polymorphism and
papillary thyroid carcinoma

WANG Chong1,LIU Xiao-li2,SHI Jie-ping1,WU Yan-hua1,WANG Shi-bing1,YU Ya-qin1,SUN Hui2   

  1. 1. Department of Epidemiology and Health Statistics,School of Public Health,Jilin University,Changchun 130021,China;2. Department of Thyroid Surgery,China-Japan Union Hospital,Jilin University,Changchun 130033,China
  • Received:2012-12-12 Online:2013-03-28 Published:2013-03-28

摘要: 目的:探讨RET基因第11外显子上rs1799939位点基因多态性与甲状腺乳头状癌(PTC)的关系,为PTC的遗传学机制研究提供理论依据。方法:采用病例-对照研究方法,选取100例PTC患者作为病例组,选取与病例组患者年龄、性别匹配的100例健康人作为对照组,采用PCR-RELP方法检测病例组和对照组的基因型,应用SPSS 13.0统计软件分析该单核苷酸多态性(SNPs)位点与甲状腺癌的关联性。结果:病例组和对照组在rs1799939位点上的基因型频数分布均符合Hardy-Weinberg平衡定律(P>0.05);病例组和对照组rs1799939位点的基因型和等位基因频数分布差异无统计学意义(P>0.05);不同性别的甲状腺乳头状癌患者在该位点的基因型和等位基因频数分布差异亦无统计学意义(P>0.05)。结论:RET基因rs1799939位点的基因多态性可能与PTC的发生无关联。

关键词: RET基因, 甲状腺肿瘤, 基因多态性

Abstract: Abstract:Objective To investigate the association between the gene polymorphisms of rs1799939 site of RET exon 11 and papillary thyroid carcinoma(PTC),and to provide theoretical basis for genetic mechanism of PTC.Methods A case-control  study was used in this research.100 cases of PTC were selected as case group,100 healthy people matched in age and sex were selected as control group.PCR-RELP analysis was employed to detect the genotypes of the two groups,statistical analysis software SPSS 13.0 was used to analyze the association between the gene polymorphisms of rs1799939 site and PTC.Results The distribution of genotypic frequency of rs1799939 site didn’t deviate from Hardy-Weinberg equilibrium in both case group and control group (P>0.05).The distribution of genotypic and allelic frequencies at rs1799939 site showed no statistical significance between case group and control group (P>0.05).The distribution of genotypic and allelic frequencies between different genders in case group showed no statistical significance either (P>0.05).Conclusion The polymorphism of rs1799939 site in the RET gene may be not associated with the occurrence of PTC.

Key words: RET gene, thyroid neoplasms, genepolymorphism

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