University of British Columbia, Child & Family Research Institute, Room A5-147, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada.
Curr Opin Oncol. 2013 Sep;25(5):495-502. doi: 10.1097/CCO.0b013e328363dfee.
The development of HIV protease inhibitors more than two decades ago heralded a new era in HIV care, changing the infection from universally fatal to chronic but controllable. With the widespread use of protease inhibitors, there was a reduction in the incidence and mortality of HIV-associated malignancies. Studies later found these drugs to have promising direct antitumor effects.
Protease inhibitors have a wide range of effects on several cellular pathways that are important for tumorigenesis and independent of inhibition of the HIV protease, including reducing angiogenesis and cell invasion, inhibition of the Akt pathway, induction of autophagy, and promotion of apoptosis. Among protease inhibitors, nelfinavir appears to have the most potent and broad antineoplastic activities, and also affects replication of the oncogenic herpesviruses Kaposi sarcoma-associated herpesvirus and Epstein-Barr virus. Nelfinavir is being studied for the prevention and treatment of a wide range of malignancies in persons with and without HIV infection.
Nelfinavir and other protease inhibitors are well tolerated, oral drugs that have promising antitumor properties, and may prove to play an important role in the prevention and treatment of several cancers. Additional insights into protease inhibitors' mechanisms of action may lead to the development of novel cancer chemotherapy agents.
二十多年前 HIV 蛋白酶抑制剂的发展开创了 HIV 治疗的新时代,将该感染从普遍致命转变为慢性但可控制的疾病。随着蛋白酶抑制剂的广泛使用,HIV 相关恶性肿瘤的发病率和死亡率均有所降低。随后的研究发现这些药物具有有前途的直接抗肿瘤作用。
蛋白酶抑制剂对肿瘤发生过程中多个重要的细胞通路具有广泛的影响,其作用不仅限于抑制 HIV 蛋白酶,包括减少血管生成和细胞侵袭、抑制 Akt 通路、诱导自噬和促进细胞凋亡。在蛋白酶抑制剂中,奈非那韦似乎具有最强和最广泛的抗肿瘤活性,并且还影响致瘤性疱疹病毒卡波西肉瘤相关疱疹病毒和 Epstein-Barr 病毒的复制。奈非那韦目前正在研究用于预防和治疗 HIV 感染者和非感染者的多种恶性肿瘤。
奈非那韦和其他蛋白酶抑制剂是耐受性良好的口服药物,具有有前途的抗肿瘤特性,可能在预防和治疗多种癌症方面发挥重要作用。对蛋白酶抑制剂作用机制的进一步了解可能会导致新型癌症化疗药物的开发。