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去甲基化治疗作为一种针对人乳头瘤病毒相关头颈部癌症的靶向治疗方法。

Demethylation Therapy as a Targeted Treatment for Human Papillomavirus-Associated Head and Neck Cancer.

机构信息

Department of Surgery, Division of Otolaryngology, Yale University, New Haven, Connecticut.

Department of Medicine, Division of Medical Oncology, Yale University, New Haven, Connecticut.

出版信息

Clin Cancer Res. 2017 Dec 1;23(23):7276-7287. doi: 10.1158/1078-0432.CCR-17-1438. Epub 2017 Sep 15.

Abstract

DNA methylation in human papillomavirus-associated (HPV) head and neck squamous cell carcinoma (HNSCC) may have importance for continuous expression of HPV oncogenes, tumor cell proliferation, and survival. Here, we determined activity of a global DNA-demethylating agent, 5-azacytidine (5-aza), against HPV HNSCC in preclinical models and explored it as a targeted therapy in a window trial enrolling patients with HPV HNSCC. Sensitivity of HNSCC cells to 5-aza treatment was determined, and then 5-aza activity was tested using xenografted tumors in a mouse model. Finally, tumor samples from patients enrolled in a window clinical trial were analyzed to identify activity of 5-aza therapy in patients with HPV HNSCC. Clinical trial and experimental data show that 5-aza induced growth inhibition and cell death in HPV HNSCC. 5-aza reduced expression of HPV genes, stabilized p53, and induced p53-dependent apoptosis in HNSCC cells and tumors. 5-aza repressed expression and activity of matrix metalloproteinases (MMP) in HPV HNSCC, activated IFN response in some HPV head and neck cancer cells, and inhibited the ability of HPV xenografted tumors to invade mouse blood vessels. 5-aza may provide effective therapy for HPV-associated HNSCC as an alternative or complement to standard cytotoxic therapy. .

摘要

人乳头瘤病毒(HPV)相关头颈部鳞状细胞癌(HNSCC)中的 DNA 甲基化可能对 HPV 致癌基因的持续表达、肿瘤细胞增殖和存活具有重要意义。在这里,我们在临床前模型中确定了一种全身性 DNA 去甲基化剂 5-氮杂胞苷(5-aza)对 HPV HNSCC 的活性,并在纳入 HPV HNSCC 患者的窗口试验中探索其作为靶向治疗的可能性。首先确定 HNSCC 细胞对 5-aza 治疗的敏感性,然后使用小鼠模型中的异种移植肿瘤测试 5-aza 的活性。最后,分析纳入窗口临床试验的患者的肿瘤样本,以确定 5-aza 治疗 HPV HNSCC 患者的活性。临床和实验数据表明,5-aza 可诱导 HPV HNSCC 生长抑制和细胞死亡。5-aza 降低 HPV 基因的表达,稳定 p53,并诱导 HNSCC 细胞和肿瘤中的 p53 依赖性细胞凋亡。5-aza 抑制 HPV HNSCC 中基质金属蛋白酶(MMP)的表达和活性,在一些 HPV 头颈部癌细胞中激活 IFN 反应,并抑制 HPV 异种移植肿瘤侵犯小鼠血管的能力。5-aza 可能为 HPV 相关的 HNSCC 提供有效的治疗选择,作为标准细胞毒性治疗的替代或补充。

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