High-throughput screening identifies candidate drugs for the treatment of recurrent respiratory papillomatosis

被引:18
作者
Alkhilaiwi, Faris [1 ,2 ,3 ,5 ]
Paul, Siddartha [1 ]
Zhou, Dan [1 ]
Zhang, Xiaohu [6 ]
Wang, Feibai [1 ]
Palechor-Ceron, Nancy [1 ]
Wilson, Kelli [6 ]
Guha, Rajarshi [6 ]
Ferrer, Marc [6 ]
Grant, Nazaneen [4 ]
Thomas, Craig [6 ]
Schlegel, Richard [1 ]
Yuan, Hang [1 ]
机构
[1] Georgetown Univ, Sch Med, Dept Pathol, Washington, DC 20057 USA
[2] Georgetown Univ, Sch Med, Dept Oncol, Washington, DC 20057 USA
[3] Georgetown Univ, Sch Med, Dept Biochem & Mol Biol, Washington, DC 20057 USA
[4] Georgetown Univ, Sch Med, Dept Otolaryngol, Washington, DC 20057 USA
[5] King Abdulaziz Univ, Coll Pharm, Jeddah, Saudi Arabia
[6] NIH, Div Preclin Innovat, Natl Ctr Adv Translat Sci, Bldg 10, Bethesda, MD 20892 USA
来源
PAPILLOMAVIRUS RESEARCH | 2019年 / 8卷
关键词
Primary cell culture; Recurrent respiratory papillomatosis; High-throughput screening; Panobinostat; Dinaciclib; Forskolin; Drug sensitivity; Repurposing; CONDITIONALLY REPROGRAMMED CELLS; HPV-DNA; INHIBITOR; FORSKOLIN; APOPTOSIS; OSTEOSARCOMA; STATE;
D O I
10.1016/j.pvr.2019.100181
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recurrent respiratory papillomatosis (RRP) is a benign neoplasm of the larynx caused mainly by human papillomavirus type 6 or 11 and its standard treatment involves repeated surgical debulking of the laryngeal tumors. However, significant morbidity and occasional mortality due to multiple recurrences occur. Conditional reprogramming (CR) was used to establish a HPV-6 positive culture from an RRP patient, named GUMC-403. High-throughput screening was performed at the National Center for Advanced Technology (NCATS) to identify potential drugs to treat this rare but morbid disease. GUMC-403 cells were screened against the NPC library of > 2800 approved drugs and the MIPE library of > 1900 investigational drugs to identify new uses for FDA-approved drugs or drugs that have undergone significant research and development. From the two libraries, we identified a total of 13 drugs that induced significant cytotoxicity in RRP cells at IC50 values that were clinically achievable. We validated the efficacy of the drugs in vitro using CR 2D and 3D models and further refined our list of drugs to panobinostat, dinaciclib and forskolin as potential therapies for RRP patients.
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页数:10
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