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胃癌线粒体基因组控制区变异和不稳定性的研究
引用本文:韩琤波,李凡,毛晓韵,马佳明,赵雨杰,辛彦. 胃癌线粒体基因组控制区变异和不稳定性的研究[J]. 中华肿瘤防治杂志, 2004, 11(10): 1017-1020
作者姓名:韩琤波  李凡  毛晓韵  马佳明  赵雨杰  辛彦
作者单位:中国医科大学附属第一医院肿瘤研究所第四研究室,辽宁,沈阳,110001;中国医科大学高职学院医学基础教研室,辽宁,沈阳,110001;中国医科大学生物芯片中心,辽宁,沈阳,110001
基金项目:国家自然科学基金(30371607)
摘    要:目的 :检测胃癌线粒体基因组的控制区 (controlregion)的不稳定性、多态性及其他变异 ,探讨其与胃癌的关系。方法 :对2 2例胃癌患者的癌组织及其癌旁正常组织共 44个样本的线粒体DNA (mitochondrialDNA ,mtDNA)的控制区通过PCR扩增 ;然后通过直接测序检测控制区的不稳定性、多态性以及其他变异。结果 :mtDNA控制区不稳定性在胃癌组织和癌旁正常黏膜组织间无明显差异 ,分别为 5 9 1% ( 13 /2 2 )和40 9% ( 9/2 2 ) ,P =0 3 7;并且与胃癌分化程度也不相关 ,P =0 42。 7例样本显示np16182PolyC不稳定性 ,其中 5例伴有np16189T C的转换。另外研究还发现了一些新的控制区变异。结论 :线粒体DNA控制区变异和不稳定性对胃癌发生的作用有限。np165 69T C的转换很可能是np 16182PolyC不稳定性的重要原因之一

关 键 词:DNA  线粒体  基因组  胃肿瘤  变异
文章编号:1009-4571(2004)10-1017-04
修稿时间:2004-04-15

Study on variations and instabilities of mitochondrial control region in gastric cancer
HAN Cheng-bo ,LI Fan ,MAO Xiao-yun ,MA Jiaming ,ZHAO Yu-jie ,XIN Yan .Cancer Institute,No. Hospital,China Medical University,Shenyang ,P.R. China .High Professional Technical Institute,China Medical University,Shenyang ,P.R. China .Biochip Center,China Medical University,Shenyang ,P.R.China. Study on variations and instabilities of mitochondrial control region in gastric cancer[J]. Chinese Journal of Cancer Prevention and Treatment, 2004, 11(10): 1017-1020
Authors:HAN Cheng-bo   LI Fan   MAO Xiao-yun   MA Jiaming   ZHAO Yu-jie   XIN Yan .Cancer Institute  No. Hospital  China Medical University  Shenyang   P.R. China .High Professional Technical Institute  China Medical University  Shenyang   P.R. China .Biochip Center  China Medical University  Shenyang   P.R.China
Affiliation:HAN Cheng-bo 1,LI Fan 2,MAO Xiao-yun 1,MA Jiaming 3,ZHAO Yu-jie 3,XIN Yan 1 1.Cancer Institute,No.1 Hospital,China Medical University,Shenyang 110001,P.R. China 2.High Professional Technical Institute,China Medical University,Shenyang 110001,P.R. China 3.Biochip Center,China Medical University,Shenyang 110001,P.R.China
Abstract:OBJECTIVE: To detect the instabilities, polymorphisms and other variations of mitochondrial DNA (mtDNA) control region in gastric cancers, and study the relationships between them and gastric cancer.METHODS:mtDNA control region was detected for instabilities, polymorphisms and other variations via PCR amplification followed by direct DNA sequencing in 22 matched gastric cancerous and paracancerous tissues. RESULTS:There was no statistic significance in variations of mtDNA control region between gastric cancerous tissues and matched paracancerous tissues, 40.9% (9/22) and 59.1% (13/22) respectively, P=0.37, nor was there between highly differentiated gastric cancers and the lowly differentiated gastric cancers, P=0.42. np16182 polyC instabilities were found in seven samples, five of which simultaneously had a np 16 189 T-C transition. Some new variations were found. CONSLUSIONS:There is no relationship between gastric cancerigenesis and variations or instabilities of mtDNA control region. np 16 189 T-C transition may be an important factor of polyC instability in gastric cancer.
Keywords:DNA   mitochondrial  genome  stomach neoplasms  variations
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