Chitsike Lennox, Duerksen-Hughes Penelope J
Department of Basic Sciences, Loma Linda University School of Medicine, 11021 Campus Street, 101 Alumni Hall, Loma Linda, CA 92354, USA.
Molecules. 2021 May 18;26(10):3004. doi: 10.3390/molecules26103004.
Advanced cervical cancer is primarily managed using cytotoxic therapies, despite evidence of limited efficacy and known toxicity. There is a current lack of alternative therapeutics to treat the disease more effectively. As such, there have been more research endeavors to develop targeted therapies directed at oncogenic host cellular targets over the past 4 decades, but thus far, only marginal gains in survival have been realized. The E6 oncoprotein, a protein of human papillomavirus origin that functionally inactivates various cellular antitumor proteins through protein-protein interactions (PPIs), represents an alternative target and intriguing opportunity to identify novel and potentially effective therapies to treat cervical cancer. Published research has reported a number of peptide and small-molecule modulators targeting the PPIs of E6 in various cell-based models. However, the reported compounds have rarely been well characterized in animal or human subjects. This indicates that while notable progress has been made in targeting E6, more extensive research is needed to accelerate the optimization of leads. In this review, we summarize the current knowledge and understanding of specific E6 PPI inhibition, the progress and challenges being faced, and potential approaches that can be utilized to identify novel and potent PPI inhibitors for cervical cancer treatment.
尽管有证据表明细胞毒性疗法疗效有限且毒性已知,但晚期宫颈癌主要还是采用这种疗法进行治疗。目前缺乏能更有效治疗该疾病的替代疗法。因此,在过去40年里,人们开展了更多研究,致力于开发针对致癌宿主细胞靶点的靶向疗法,但迄今为止,仅在生存率方面取得了微乎其微的提高。E6癌蛋白是一种源自人乳头瘤病毒的蛋白质,它通过蛋白质-蛋白质相互作用(PPI)在功能上使各种细胞抗肿瘤蛋白失活,这代表了一个替代靶点,也是识别治疗宫颈癌的新型且可能有效的疗法的诱人机会。已发表的研究报告了在各种基于细胞的模型中,许多靶向E6的PPI的肽和小分子调节剂。然而,所报道的化合物在动物或人类受试者中很少得到充分表征。这表明,虽然在靶向E6方面已取得显著进展,但仍需要更广泛的研究来加速先导化合物的优化。在这篇综述中,我们总结了目前对特定E6 PPI抑制的认识和理解、面临的进展和挑战,以及可用于识别治疗宫颈癌的新型强效PPI抑制剂的潜在方法。