首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Detection of hepatitis C virus RNA using ligation-dependent polymerase chain reaction in formalin-fixed paraffin-embedded liver tissues.
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Detection of hepatitis C virus RNA using ligation-dependent polymerase chain reaction in formalin-fixed paraffin-embedded liver tissues.

机译:使用连接依赖性聚合酶链反应在福尔马林固定石蜡包埋的肝组织中检测丙型肝炎病毒RNA。

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摘要

Reverse transcription polymerase chain reaction (RT-PCR) has been used to detect hepatitis C virus (HCV) sequences in liver tissue. However, RT-PCR has a variable detection sensitivity, especially on routinely processed formalin-fixed, paraffin-embedded (FFPE) specimens. RNA-RNA and RNA-protein cross-links formed during formalin fixation is the major limiting factor preventing reverse trans criptase from extending the primers. To overcome this problem, we applied the ligation-dependent PCR (LD-PCR) for the detection of HCV RNA in FFPE liver tissue. This method uses two capture probes for RNA isolation and two hemiprobes for the subsequent PCR. Despite cross-links, the capture probes and the hemiprobes are able to form hybrids with HCV RNAs released from the FFPE tissue. The hybrids are isolated through binding of the capture probes to paramagnetic beads. The hemiprobes are then ligated by a T4 DNA ligase to form a full probe that serves as a template for the Taq DNA polymerase. A total of 22 FFPE liver specimens, 21 with hepatocellular carcinoma (HCC) and 1 with biliary cirrhosis secondary to bile duct atresia were selected for this study, of which 13 patients were HCV seropositive and 9 seronegative. HCV RNA was detectable by ID-PCR from all 13 HCV-seropositive HCCs and from 5 of 8 HCV-seronegative HCCs but not from the HCV-seronegative liver with biliary atresia. By contrast, RT-PCR detected HCV sequences in only 5 of the HCV-sero-positive and in 1 of the HCV-seronegative HCCs. To resolve the discordance between the LD-PCR and RT-PCR results, RT-PCR was performed on frozen liver tissue of the discrepant specimens, which confirmed the LD-PCR positive results. In conclusion, LD-PCR is a more sensitive method than RT-PCR for the detection of HCV sequences in routinely processed liver tissues. A high rate of HCV infection (86%) is found in HCC specimens, indicating a previously underestimated role of HCV in HCC pathogenesis.
机译:逆转录聚合酶链反应(RT-PCR)已用于检测肝组织中的丙型肝炎病毒(HCV)序列。但是,RT-PCR具有可变的检测灵敏度,尤其是在常规处理的福尔马林固定,石蜡包埋(FFPE)样品上。在福尔马林固定过程中形成的RNA-RNA和RNA-蛋白质交联是阻止逆转录酶扩展引​​物的主要限制因素。为了克服这个问题,我们将连接依赖PCR(LD-PCR)用于检测FFPE肝组织中的HCV RNA。此方法使用两个捕获探针进行RNA分离,并使用两个半探针进行后续PCR。尽管有交联,捕获探针和半探针仍能够与从FFPE组织释放的HCV RNA形成杂种。通过将捕获探针与顺磁珠结合来分离杂交体。然后将半探针与T4 DNA连接酶连接,形成完整的探针,用作Taq DNA聚合酶的模板。总共选择了22份FFPE肝标本,21例肝细胞癌(HCC)和1例因胆管闭锁继发的胆汁性肝硬化,其中13例HCV血清阳性和9例血清阴性。可以通过ID-PCR从所有13种HCV血清阳性的HCC和8种HCV血清阴性的HCC中的5种检测到HCV RNA,但从胆道闭锁的HCV血清阴性的肝中则无法检测到。相比之下,RT-PCR仅在5例HCV血清阳性和1例HCV血清阴性的HCC中检测到HCV序列。为了解决LD-PCR和RT-PCR结果之间的不一致,对差异标本的冷冻肝组织进行了RT-PCR,证实了LD-PCR的阳性结果。总之,对于常规处理的肝组织中的HCV序列检测,LD-PCR比RT-PCR更为灵敏。在HCC标本中发现高HCV感染率(86%),这表明HCV在HCC发病机理中的作用被低估了。

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