Department of Genome Modifications and Carcinogenesis (F020), Research Program Infection and Cancer, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Mol Cell Probes. 2011 Apr-Jun;25(2-3):108-13. doi: 10.1016/j.mcp.2011.03.003. Epub 2011 Mar 23.
Infections with high-risk human papillomaviruses (HPV), mainly HPV type 16, can cause malignant transformation of the human cervical epithelium and cervical cancer (CxCa). Very little is known about the quantitative expression of the various HPV16 transcripts in frequently used cervical cancer cell lines.
We have quantitatively analysed the viral transcriptome in the HPV16-transformed cell lines SiHa, CaSki, MRI-H196, MRI-H186, HPK-IA and C3. We used a nucleic acid sequence-based amplification (NASBA)-Luminex hybridisation assay quantifying spliced and unspliced HPV16 transcripts.
The cell lines differed in their qualitative and quantitative expression of viral transcripts depending on the physical HPV genome status. In SiHa, we found no transcripts containing the splice acceptor at nucleotide 3358 or downstream sequences. In CaSki cells virtually all viral transcripts were detected but with a reduced quantity of late transcripts. We further found that the tumorigenic phenotype of late passage HPK-IA cells may not be mediated through changes in HPV expression. In MRI-H186, HPK-IA and C3 cells very high levels of full-length early transcripts ending at the early polyadenylation signal were found. MRI-H196 expressed L1 full-length (fl) but no E5 fl RNA suggesting the presence of integrated HPV16 genomes with a disrupted E2 region and rearranged L1 DNA sequence.
Quantitative expression changes of HPV16 transcript markers correlate with the physical state of the HPV genome in HPV16 positive cervical cancer cell lines.
高危型人乳头瘤病毒(HPV),主要是 HPV 16 型,可引起人体宫颈上皮的恶性转化和宫颈癌(CxCa)。目前对于常用的宫颈癌细胞系中 HPV16 各种转录本的定量表达知之甚少。
我们定量分析了 HPV16 转化细胞系 SiHa、CaSki、MRI-H196、MRI-H186、HPK-IA 和 C3 中的病毒转录组。我们使用核酸序列扩增(NASBA)-Luminex 杂交测定法来定量检测剪接和未剪接的 HPV16 转录本。
根据 HPV 基因组的物理状态,细胞系在病毒转录本的定性和定量表达上存在差异。在 SiHa 细胞中,我们没有发现包含核苷酸 3358 处剪接受体或下游序列的转录本。在 CaSki 细胞中几乎检测到所有的病毒转录本,但晚期转录本的数量减少。我们进一步发现,晚期传代的 HPK-IA 细胞的致瘤表型可能不是通过 HPV 表达的变化介导的。在 MRI-H186、HPK-IA 和 C3 细胞中,发现了非常高水平的全长早期转录本,这些转录本的末端位于早期多聚腺苷酸化信号处。MRI-H196 表达 L1 全长(fl)但没有 E5 fl RNA,这表明存在 HPV16 基因组整合,其 E2 区缺失且 L1 DNA 序列发生重排。
HPV16 转录本标志物的定量表达变化与 HPV16 阳性宫颈癌细胞系中 HPV 基因组的物理状态相关。