Department of Human Oncology, University of Wisconsin Comprehensive Cancer Center, 3107 WIMR, 1111 Highland Avenue, Madison, WI 53705, USA.
Cancer Res. 2013 Aug 1;73(15):4791-800. doi: 10.1158/0008-5472.CAN-13-0587. Epub 2013 Jun 7.
Patients with human papillomavirus (HPV+)-associated head and neck cancer (HNC) show significantly improved survival outcome compared with those with HPV-negative (HPV-) tumors. Published data examining this difference offers conflicting results to date. We systematically investigated the radiation sensitivity of all available validated HPV+ HNC cell lines and a series of HPV- HNC cell lines using in vitro and in vivo techniques. HPV+ HNCs exhibited greater intrinsic radiation sensitivity (average SF2 HPV-: 0.59 vs. HPV+: 0.22; P < 0.0001), corresponding with a prolonged G2-M cell-cycle arrest and increased apoptosis following radiation exposure (percent change 0% vs. 85%; P = 0.002). A genome-wide microarray was used to compare gene expression 24 hours following radiation between HPV+ and HPV- cell lines. Multiple genes in TP53 pathway were upregulated in HPV+ cells (Z score 4.90), including a 4.6-fold increase in TP53 (P < 0.0001). Using immortalized human tonsillar epithelial (HTE) cells, increased radiation sensitivity was seen in cell expressing HPV-16 E6 despite the effect of E6 to degrade p53. This suggested that low levels of normally functioning p53 in HPV+ HNC cells could be activated by radiation, leading to cell death. Consistent with this, more complete knockdown of TP53 by siRNA resulted in radiation resistance. These results provide clear evidence, and a supporting mechanism, for increased radiation sensitivity in HPV+ HNC relative to HPV- HNC. This issue is under active investigation in a series of clinical trials attempting to de-escalate radiation (and chemotherapy) in selected patients with HPV+ HNC in light of their favorable overall survival outcome.
与 HPV 阴性(HPV-)肿瘤相比,人乳头瘤病毒(HPV)相关头颈部癌症(HNC)患者的生存结果明显改善。迄今为止,已发表的检查这种差异的数据提供了相互矛盾的结果。我们系统地使用体外和体内技术研究了所有可用的已验证 HPV+ HNC 细胞系和一系列 HPV- HNC 细胞系的辐射敏感性。HPV+ HNC 表现出更高的内在辐射敏感性(平均 SF2 HPV-:0.59 与 HPV+:0.22;P <0.0001),这与辐射后 G2-M 细胞周期停滞和细胞凋亡增加相对应(百分比变化 0%与 85%;P = 0.002)。使用全基因组微阵列比较了 HPV+和 HPV-细胞系在辐射后 24 小时的基因表达。TP53 通路中的多个基因在 HPV+细胞中上调(Z 分数 4.90),包括 TP53 增加 4.6 倍(P <0.0001)。使用永生化人扁桃体上皮(HTE)细胞,尽管 HPV-16 E6 的作用是降解 p53,但在表达 HPV-16 E6 的细胞中观察到辐射敏感性增加。这表明 HPV+ HNC 细胞中正常功能的 p53 水平可能被辐射激活,导致细胞死亡。与此一致的是,通过 siRNA 更完全地敲低 TP53 导致辐射抗性。这些结果提供了明确的证据和支持机制,证明 HPV+ HNC 相对于 HPV- HNC 的辐射敏感性增加。鉴于 HPV+ HNC 患者的总体生存结果良好,这一问题正在一系列临床试验中积极研究,试图在选定的 HPV+ HNC 患者中减少辐射(和化疗)的剂量。