Rhee Juong G, Li DaQing, O'Malley Bert W, Suntharalingam Mohan
Department of Radiation Oncology, University of Maryland School of Medicine, BRB 6013, 655 West Baltimore Street, Baltimore, MD 21201, USA.
ORL J Otorhinolaryngol Relat Spec. 2003 May-Jun;65(3):144-54. doi: 10.1159/000072252.
Since adenoviral P16(INK4A) gene transfer has shown limited promise in preclinical studies, we developed a strategy combining ionizing radiation (x-rays) with Ad-P16 gene therapy. Both radiation (2 Gy) and Ad-P16 alone demonstrated anti-tumor responses. The combination of radiation and Ad-P16 in vitro showed an augmented therapeutic response. Two head and neck squamous cell carcinoma (HNSCC) cell lines treated with Ad-P16 demonstrated positive staining to annexin V and terminal deoxynucleotidyl-transferase, suggesting apoptosis. When the HNSCC cell lines were grown in nude mice, the anti-tumor response by Ad-P16, radiation, and combination therapy ranged from limited benefit of the single-agent therapy to a statistically significant additive response to combination therapy. Our data suggest that Ad-P16 gene therapy may prove effective in treating human HNSCC that is refractory to radiation therapy.
由于腺病毒P16(INK4A)基因转移在临床前研究中显示出有限的前景,我们开发了一种将电离辐射(X射线)与Ad-P16基因治疗相结合的策略。单独的辐射(2 Gy)和Ad-P16都表现出抗肿瘤反应。辐射与Ad-P16在体外联合显示出增强的治疗反应。用Ad-P16处理的两种头颈部鳞状细胞癌(HNSCC)细胞系对膜联蛋白V和末端脱氧核苷酸转移酶呈阳性染色,提示细胞凋亡。当HNSCC细胞系在裸鼠体内生长时,Ad-P16、辐射及联合治疗的抗肿瘤反应范围从单药治疗的有限益处到联合治疗的统计学显著相加反应。我们的数据表明,Ad-P16基因治疗可能被证明对治疗对放射治疗难治的人类HNSCC有效。