反向点杂交法快速检测HPV基因型的临床应用
DOI:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:


Rapid Detection and Typing of Human Papillomavirus in Tumor Tissue by Reverse Dot Blot Technique
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    应用反向点杂交法(RDB)的原理,针对HPV 6B, 11, 16, 18, 31, 33和35设计了7条序列作为未标记的特异性寡核苷酸(SSO)探针,分别固定在尼龙膜条上,形成7个点,再与经PCR扩增的样品DNA序列杂交,即可在一个膜条上分辨出这7型HPV中的任一型.此法快速简便,特异性高,不存在假阳性;且因PCR灵敏度高,亦不易出现假阴性.用PCR-RDB法检测保存的宫颈癌组织石蜡包埋标本32例,结果:HPV16阳性22例(68.8%),HPV18阳性5例(15.6%),HPV16/18双重感染2例(6.3%),阴性仅3例(9.3%).

    Abstract:

    Reverse dot blot (RDB) technique was used. Seven sequence-specific oligonucleotide (SSO) probes directed against 7 types of HPV (HPV6B, 11, 16, 18, 31, 33 and 35) respectively are synthesized and fixed sequentially on a stripe of nylon membrane to form 7 spots. After hybridization with the PCR product of the sample DNA sequence, any one of the 7 types of HPV DNA were distinguished on only one stripe of nylon membrane. 38 cases of cervical carcinoma samples were detected by this PCR-RDB technique. The results show: 29 cases (76.3%) of HPV16 positive; 8 cases (21.1%) of HPV18 positive; 2 cases (7.2%)of double infection; and 3 cases (8.0%) of HPV negative.The method is rapid and simple, with high specificity, no false positive results in general, and as the PCR technique is very sensitive, the method is not liable to show false negative results.

    参考文献
    相似文献
    引证文献
引用本文

齐凤菊,徐钤,黄扬中.反向点杂交法快速检测HPV基因型的临床应用[J].生物化学与生物物理进展,1998,25(1):75-78

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:1996-12-02
  • 最后修改日期:1997-03-16
  • 接受日期:
  • 在线发布日期:
  • 出版日期: