Huber Evamaria, Vlasny Daniela, Jeckel Sonja, Stubenrauch Frank, Iftner Thomas
Sektion Experimentelle Virologie, Universitaetsklinikum Tuebingen, 72076 Tuebingen, Germany.
J Virol. 2004 Jul;78(14):7478-89. doi: 10.1128/JVI.78.14.7478-7489.2004.
To investigate changes in cellular gene expression associated with malignant progression, we identified differentially expressed genes in a cottontail rabbit papillomavirus (CRPV) squamous carcinoma model employing New Zealand White rabbits. The technique of suppression subtractive cDNA hybridization was applied to pairs of mRNA isolates from CRPV-induced benign papillomas and carcinomas, with each pair derived from the same individual rabbit. The differential expression of 23 subtracted cDNAs was further confirmed by quantitative reverse transcription-PCR (RT-PCR) with additional biopsies. Eight papilloma-carcinoma pairs examined showed a constant upregulation of the transcripts for the multifunctional adaptor protein 14-3-3 zeta and the Y-box binding transcription factor YB-1, whereas transcripts for m-type calpain 2 and NB thymosin beta, which are involved in cell motility and tissue invasion, as well as casein kinase 1 alpha, chaperonin, and annexin I, were found to be upregulated in the majority of the cases. RNA-RNA in situ hybridization and laser capture microdissection in combination with quantitative RT-PCR analysis verified the deregulated expression of the transcripts in the tumor cells. In contrast, CRPV E7 transcript levels remained rather constant indicating no requirement for a further upregulation of E7 expression following tumor induction. Small interfering RNA-mediated interference with expression of genes encoding YB-1, m-type calpain 2, or NB thymosin beta in a CRPV-positive cell line established from New Zealand White rabbit keratinocytes resulted in decreased cell invasion in matrigel chamber assays.
为了研究与恶性进展相关的细胞基因表达变化,我们在采用新西兰白兔的棉尾兔乳头瘤病毒(CRPV)鳞状细胞癌模型中鉴定了差异表达基因。抑制性消减cDNA杂交技术应用于来自CRPV诱导的良性乳头瘤和癌的mRNA分离物对,每对均来自同一只兔子。通过对额外活检样本进行定量逆转录PCR(RT-PCR)进一步证实了23个消减cDNA的差异表达。所检测的8对乳头瘤-癌样本显示多功能衔接蛋白14-3-3ζ和Y盒结合转录因子YB-1的转录本持续上调,而参与细胞运动和组织侵袭的m型钙蛋白酶2和NB胸腺素β以及酪蛋白激酶1α、伴侣蛋白和膜联蛋白I的转录本在大多数病例中上调。RNA-RNA原位杂交以及激光捕获显微切割结合定量RT-PCR分析证实了肿瘤细胞中转录本的表达失调。相比之下,CRPV E7转录水平保持相当稳定,表明肿瘤诱导后E7表达无需进一步上调。在从新西兰白兔角质形成细胞建立的CRPV阳性细胞系中,小干扰RNA介导的对编码YB-1、m型钙蛋白酶2或NB胸腺素β的基因表达的干扰导致基质胶小室试验中的细胞侵袭减少。