作为分子黑客的HPV:对HPV驱动的主机监管网络中HPV驱动的变化的计算探索
Massimiliano Chetta1, Alessandra Rosati2, Nenad Bukvic3
1Azienda Ospedaliera di rilievo nazionale "A. Cardarelli Hospital's" Laboratory of Medical Genetics and Genomics, 80131 Naples, Italy.
Viruses
|September 27, 2025
概括
人类乳头瘤病毒 (HPV) 基因组图案可能会诱惑人类转录因子,破坏基因调节并促进癌症. 这项研究确定了新的病毒宿主相互作用和潜在的治疗点.
科学领域:
- 病毒学 病毒学
- 分子生物学分子生物学
- 计算生物学 计算生物学
背景情况:
- 人类乳头瘤病毒 (HPV) 导致宫癌和其他癌症.
- 已知的HPV瘤蛋白E6和E7是已知的瘤基因.
- HPV 对宿主基因调节的更广泛影响尚不清楚.
研究的目的:
- 调查HPV基因组图案是否作为人类转录因子的诱.
- 探索这些相互作用如何破坏宿主基因调节并导致癌症.
- 在这些病毒与宿主相互作用中确定潜在的治疗点.
主要方法:
- 使用MEME-ChIP和Tomtom.tom进行高风险HPV基因组的计算分析.
- 用STRING进行蛋白质与蛋白质相互作用分析.
- 用Enrichr.r.进行生物通路丰富分析.
主要成果:
- 确定了结合人类转录因子 (FOX,HOX,NFAT家族,指蛋白) 的保存型HPV动机.
- 在SMARCA1,DUX4,CDX1和HPV驱动的转化之间发现了新的关联.
- 途径分析表明参与Wnt信号传递,与癌症相关的转录错误调节和染色质重塑.
结论:
- HPV利用保存的基因组动机来隔离转录因子,改变宿主基因表达.
- 这些相互作用通过Wnt信号和染色体重塑等途径促进瘤发生.
- 形方法揭示了HPV相关的恶性瘤的新治疗点.
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