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棉尾兔乳头瘤病毒诱导的癌组织基因谱分析确定了直接参与基质侵袭的上调基因,这一点通过小干扰RNA介导的基因沉默得以证实。

Gene profiling of cottontail rabbit papillomavirus-induced carcinomas identifies upregulated genes directly Involved in stroma invasion as shown by small interfering RNA-mediated gene silencing.

作者信息

Huber Evamaria, Vlasny Daniela, Jeckel Sonja, Stubenrauch Frank, Iftner Thomas

机构信息

Sektion Experimentelle Virologie, Universitaetsklinikum Tuebingen, 72076 Tuebingen, Germany.

出版信息

J Virol. 2004 Jul;78(14):7478-89. doi: 10.1128/JVI.78.14.7478-7489.2004.

Abstract

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.

摘要

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。

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