Department of Surgery, School of Medicine and Public Health, University of Wisconsin, 600 Highland Avenue, Madison, WI 53792, USA.
Carbone Cancer Center, School of Medicine and Public Health, University of Wisconsin, 600 Highland Avenue, Madison, WI 53705, USA.
Viruses. 2023 Apr 20;15(4):1013. doi: 10.3390/v15041013.
Anal cancer is a major health problem. This study seeks to determine if the topical protease inhibitor Saquinavir (SQV), is effective at the prevention of anal cancer in transgenic mice with established anal dysplasia. mice were entered into the study when the majority spontaneously developed high-grade anal dysplasia. To ensure carcinoma development, a subset of the mice was treated with a topical carcinogen: 7,12-Dimethylbenz[a]anthracene (DMBA). Treatment groups included: no treatment, DMBA only, and topical SQV with/without DMBA. After 20 weeks of treatment, anal tissue was harvested and evaluated histologically. SQV was quantified in the blood and anal tissue, and tissue samples underwent analysis for E6, E7, p53, and pRb. There was minimal systemic absorption of SQV in the sera despite high tissue concentrations. There were no differences in tumor-free survival between SQV-treated and respective control groups but there was a lower grade of histological disease in the mice treated with SQV compared to those untreated. Changes in E6 and E7 levels with SQV treatment suggest that SQV may function independently of E6 and E7. Topical SQV decreased histological disease progression in HPV transgenic mice with or without DMBA treatment without local side effects or significant systemic absorption.
肛门癌是一个主要的健康问题。本研究旨在确定局部蛋白酶抑制剂沙奎那韦(SQV)是否能有效预防已患有肛门发育不良的转基因小鼠的肛门癌。当大多数小鼠自发发展为高级别肛门发育不良时,将这些小鼠纳入研究。为了确保癌症的发展,一部分小鼠接受了局部致癌剂:7,12-二甲基苯并[a]蒽(DMBA)治疗。治疗组包括:无治疗、DMBA 单独治疗和局部 SQV 联合/不联合 DMBA 治疗。经过 20 周的治疗后,采集肛门组织并进行组织学评估。在血液和肛门组织中定量检测 SQV,对组织样本进行 E6、E7、p53 和 pRb 分析。尽管组织浓度很高,但 SQV 在血清中的全身吸收很少。与相应的对照组相比,接受 SQV 治疗的小鼠的无肿瘤生存率没有差异,但与未接受治疗的小鼠相比,接受 SQV 治疗的小鼠的疾病程度较低。SQV 治疗后 E6 和 E7 水平的变化表明,SQV 可能独立于 E6 和 E7 发挥作用。局部 SQV 可降低 HPV 转基因小鼠在接受或不接受 DMBA 治疗时的组织疾病进展,而无局部副作用或明显的全身吸收。