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DHQZ-17, a potent inhibitor of the transcription factor HNF4A, suppresses tumorigenicity of head and neck squamous cell carcinoma in vivo
- Source :
- Journal of Cellular Physiology. 233:2613-2628
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- A series of 2, 3-dihydroquinazolinone derivatives were synthesized, characterized and their anticancer activity was determined. Among the compounds synthesized and screened, one compound (17) showed potent anticancer activity against human head and neck squamous cell carcinoma cell line, SCC131 and was non-toxic to normal cells. The compound inhibited the growth of SCC131 cells, with an IC50 of 1.75 μM, triggered apoptotic mode of cell death and caused tumor regression of SCC131 tumor xenografts in athymic mice. To decipher the target for the lead compound, a high throughput qPCR array was performed. Results showed that the compound 17, inhibited the expression of a vital transcription factor HNF4A, involved in regulation of metabolic pathways. Thus, the present work has identified a lead compound 17, with potent anticancer activity, minimal normal cell toxicity and a plausible target and hence definitely holds future prospects as an anticancer agent.
- Subjects :
- 0301 basic medicine
Programmed cell death
Time Factors
Cell cycle checkpoint
Physiology
Clinical Biochemistry
Mice, Nude
Antineoplastic Agents
Apoptosis
Inhibitory Concentration 50
03 medical and health sciences
0302 clinical medicine
Cell Line, Tumor
medicine
Animals
Humans
Cytotoxicity
Transcription factor
Cell Proliferation
Quinazolinones
Dose-Response Relationship, Drug
Squamous Cell Carcinoma of Head and Neck
Chemistry
Cell growth
Cell Cycle Checkpoints
Cell Biology
medicine.disease
Xenograft Model Antitumor Assays
Head and neck squamous-cell carcinoma
030104 developmental biology
Hepatocyte Nuclear Factor 4
Head and Neck Neoplasms
Cell culture
030220 oncology & carcinogenesis
Carcinoma, Squamous Cell
Cancer research
Female
Subjects
Details
- ISSN :
- 00219541
- Volume :
- 233
- Database :
- OpenAIRE
- Journal :
- Journal of Cellular Physiology
- Accession number :
- edsair.doi.dedup.....3e18c43ed194f27f21c27db74c0d9b0c
- Full Text :
- https://doi.org/10.1002/jcp.26139