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作 者:吴秀娟[1] 石岩[1] 靳颖[1] 张德志[1] 普雄明[1]
机构地区:[1]新疆维吾尔自治区人民医院皮肤性病科,乌鲁木齐830001
出 处:《中华皮肤科杂志》2011年第11期805-807,共3页Chinese Journal of Dermatology
基 金:新疆维吾尔自治区自然科学基金(2009211A24)
摘 要:目的探讨人疱疹病毒8型(HHV-8)ORF26的单核苷酸多态性,分析其与Kaposi肉瘤不同临床分型及黏膜侵袭性的相关性。方法Kaposi肉瘤患者32例,其中经典型26例,艾滋病相关型6例。使用酚-氯仿-异戊醇方法对Kaposi肉瘤石蜡包埋组织进行HHV-8 DNA抽提,采用巢式PCR方法扩增ORF26基因并双向测序,使用DNAStar软件和Clustal W软件分析ORF26基因的单核苷酸多态性。运用Fisher确切概率法对结果进行统计学分析。结果ORF26基因研究发现,32例Kaposi肉瘤患者中HHV-8阳性30例,6例艾滋病相关型HHV-8均为阳性。30例患者的病毒株中,HHV-8 ORF26基因SNP主要集中在981T/C(12例)、1086C/T(12例)、1139A/C(12例);HHV-8 ORF26基因单核苷酸多态性在不同临床分型或有无黏膜损害的Kaposi肉瘤之间的差异无统计学意义。结论HHV-8 ORF26基因单核苷酸多态性可能与Kaposi肉瘤不同临床分型和黏膜侵袭性无关。Objective To study the single nucleotide polymorphisms (SNPs) in the ORF26 gene of HHV-8 in Kaposi's sarcoma (KS), and to assess their correlations with the clinical phenotype and mucosal invasion of KS. Methods HHV-8 DNA was extracted with phenol-chloroform-isoamyl alcohol from paraffin-era- bedded tissue specimens obtained from 32 cases of KS ORF26 gene of HHV-8 was amplified by nested-PCR (including 26 classic and 6 AIDS-related KS). The followed by bidirectional sequencing. The software DNAStar and program Clustal W were used to assess the SNPs in the ORF26 gene. Statistical analysis was carried out by using the Fisher's exact probability test. Results HHV-8 DNA was detected in 30 of the 32 tissue specimens, and in all of the 6 AIDS-related specimens. The predominant SNPs were 981 T/C (n = 12), 1086 C/T (n = 12) and 1139 A/C (n = 12) in the ORF26 gene of the 30 strains of HHV-8. No significant difference was observed in the distribution of SNPs in ORF26 between different phenotypes of KS or between KS with and without mucosal invasion. Conclusion The ORF26 SNPs of HHV-8 seem unrelated to the clinical phenotypes or mucosal invasion of KS.
关 键 词:单核苷酸多态性 人疱疹病毒8型 KAPOSI肉瘤 HHV-8 巢式PCR方法 26基因 统计学分析 临床分型
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