Dixon Eric P, King Lorraine M, Adams Melissa D, Grønn Petter, Murphy Patricia G, Brown Charlotte A, Brough George H, Skomedal Hanne, Malinowski Douglas P, Fischer Timothy J
BD Diagnostics - TriPath, 4025 Stirrup Creek Dr., Suite 400, Durham, NC, USA.
J Virol Methods. 2008 Dec;154(1-2):220-2. doi: 10.1016/j.jviromet.2008.08.002. Epub 2008 Sep 20.
Infection with high-risk human papillomavirus (HPV) is known to be associated directly with the development of cervical cancer. Recent data suggests that the detection of E6/E7 mRNA from high-risk HPV types may serve as a better diagnostic method for detecting the presence of cervical pre-cancer than HPV DNA testing. This report details a commercially available nucleic acid isolation protocol which can be used to isolate reproducibly RNA from residual BD SurePath liquid-based cytology specimens stored for up to 28 days, and have demonstrated the quality and quantity of mRNA is sufficient for detection with the NorChip PreTect HPV-Proofer assay. Of the 242 specimens tested in this study, 236 (97.5%) tested positive for U1A internal control gene expression. HPV type 16, 18, 31, 33 or 45 mRNA was detected in 16/20 (80%) of the analyzed high-grade squamous intraepithelial lesion (HSIL) specimens, with a low frequency of HPV mRNA detected in the normal lesions (3%). The presence of HPV E6 expression in a subset of HPV positive specimens was also detected by real-time RT-PCR. These findings confirm that RNA of sufficient quality can be isolated from residual BD SurePath cervical cytology specimens for use in downstream NASBA and RT-PCR-based assays.
已知高危型人乳头瘤病毒(HPV)感染与宫颈癌的发生直接相关。最近的数据表明,与HPV DNA检测相比,检测高危型HPV的E6/E7 mRNA可能是一种更好的诊断宫颈癌前病变的方法。本报告详细介绍了一种可商购的核酸分离方案,该方案可用于从保存长达28天的剩余BD SurePath液基细胞学标本中可重复地分离RNA,并已证明mRNA的质量和数量足以用于NorChip PreTect HPV-Proofer检测。在本研究中检测的242个标本中,236个(97.5%)U1A内参基因表达检测呈阳性。在16/20(80%)的经分析的高级别鳞状上皮内病变(HSIL)标本中检测到HPV 16、18、31、33或45型mRNA,在正常病变中检测到HPV mRNA的频率较低(3%)。还通过实时RT-PCR检测到一部分HPV阳性标本中存在HPV E6表达。这些发现证实,可以从剩余的BD SurePath宫颈细胞学标本中分离出质量足够的RNA,用于下游基于NASBA和RT-PCR的检测。