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肝细胞肝癌组织中丙型肝炎病毒核心区基因及其表达 …
引用本文:李江,王文亮. 肝细胞肝癌组织中丙型肝炎病毒核心区基因及其表达 …[J]. 中华实验和临床病毒学杂志, 2000, 14(1): 47-51
作者姓名:李江  王文亮
摘    要:目的 采用多种方法检测丙型肝炎病毒(HCV)核心区基因和表达产物在肝细胞肝癌(HCC)组织中的分布及其在HCC发生和发展中的作用。方法 对39例HCC患者进行免疫组化和原位杂匀的检测。IS-RT-PCR法用于检测并定位HCV-RNA。微切组织的RT-PCR法分别检测癌与癌旁组织中的HCV-RNA,以便能够控制扩增产物的来源。同时还进行 血清学ELISA和RT-PCR的检测。结果 血清ELISA的阳

关 键 词:肝细胞瘤  原位杂交  免疫组织化学  HCV  PCR
修稿时间:1999-05-27

Detectionof hepatitis C virus RNA in the tissue of hepatocellular carcinoma by multiple detectionsystem
L Li,W Wang,X Yu. Detectionof hepatitis C virus RNA in the tissue of hepatocellular carcinoma by multiple detectionsystem[J]. Chinese journal of experimental and clinical virology, 2000, 14(1): 47-51
Authors:L Li  W Wang  X Yu
Affiliation:Department of Pathology, Fourth Military Medical University, Xian 710032, China.
Abstract:OBJECTIVE: Detection of hepatic HCV RNA in hepatocellular carcinoma (HCC) is difficult, since its expression is very low. Several techniques have been established. However, false positive and negative rates still exist. In this study, we applied several conventional and recently developed detection systems to determine the exact effect of HCV RNA on the development of RCC. METHODS: Immunohistochemistry for HCV core antigen and in situ hybridization for HCV RNA had been performed in 39 cases of HCC. IS-RT-PCR was applied for detection and localization of HCV RNA. We extracted microdissected liver tissues to detect HCV RNA separately in cancerous and pericancerous tissues so that the microscopic origin of the amplicons could be controlled. The serological tests including ELISA and RT-PCR for HCV also were performed in all cases. RESULTS: The positive rate by ELISA (30.8%) was not always consistent with that by RT-PCR(43.6%)from serum samples. The latter was much more sensitive and accurate to reflect existence of HCV RNA. Immunohistochemistry showed expression of RCV core antigen in 15 of 39 HCC cases. In pericancerous tissues, the signals were mainly localized in the cytoplasm of hepatocytes. However, translocated expression of HCV core protein was observed in the nuclei of tumor cells, the translocated rate was 73.3%. According to IS-RT-PCR, the positive signals were located mainly in the cytoplasm of cancer cells, the positive rate in HCC was 53.8%, expression of HCV RNA, serum HCV RNA level was detected to be low or negative. This suggested that serum HCV RNA was not always a good reflection of hepatic HCV RNA in HCC tissues. The microdissection RT-PCR described here gave an equal positive rate (59.0%) of HCV RNA in cancerous and pericancerous tissues. CONCLUSIONS: The high detection rate of HCV RNA in HCC specimens even from seronegative patients confirms the important role of HCV RNA during malignant transformation. IS-RT-PCR is a good detection and localization method to visualize HCV RNA in HCC tissues. The microdissection RT-PCR method has a distinct advantage and we anticipate this method will provide an important evidence to determine whether HCV play a direct or indirect role in hepatocarcinogenesis.
Keywords:Hepatitis C virus  Hepatoma  in situ hybridization  Polymerase chain reaction  Immunohistochemistry
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