A novel multiplex RT-PCR system detects human endogenous retrovirus-K in breast cancer

被引:0
|
作者
H. Davari Ejthadi
J. H. Martin
J. Junying
D. A. Roden
M. Lahiri
P. Warren
P. G. Murray
P. N. Nelson
机构
[1] University of Wolverhampton,Molecular Immunology and Oncology Research Groups, Division of Biomedical Sciences
[2] University of Birmingham,Department of Pathology, Cancer Studies
来源
Archives of Virology | 2005年 / 150卷
关键词
Breast Cancer; Adriamycin; tRNA Synthetase; Cell Line T47D; Histidyl;
D O I
暂无
中图分类号
学科分类号
摘要
Human endogenous retrovirus HERV-K like-sequences have been implicated in certain cancers. We developed a novel multiplex RT-PCR system for HERV-K that yielded a 533 bp product together with a smaller sized product (319 bp) of the house keeping gene, histidyl tRNA synthetase (HtRNAS). The latter spanned an intron that also served to validate target cDNA. PCR amplicons of HERV-K and HtRNAS were visualised using a gel documentation system and the pixel intensity used to derive semi-quantitative levels of viral expression. Our data showed that HERV-K10 was significantly elevated in MCF-7 cells treated with estrogen. Interestingly, HERV-K expression was higher in MCF-7 cells selected with adriamycin. RT-PCR combined with Southern blotting also detected HERV-K from breast cancer tissue using laser capture microscopy. This study highlights the presence of HERV-K in the breast cancer cell lines MCF-7 and MCF-7 ADR and confirms HERV-K10 transcripts in the cell line T47D. We believe this study to be a novel approach in determining levels of HERV-K expression and for detecting this virus in cancer cell lines and tissues.
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页码:177 / 184
页数:7
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