Anticancer Evaluation of Novel Benzofuran-Indole Hybrids as Epidermal Growth Factor Receptor Inhibitors against Non-Small-Cell Lung Cancer Cells

The epidermal growth factor receptor (EGFR), also known as ErbB1 and HER1, belongs to the receptor tyrosine kinase family. EGFR serves as the primary driver in non-small-cell lung cancer (NSCLC) and is a promising therapeutic target for NSCLC. In this study, we synthesized a novel chemical library b...

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Main Authors: Yechan Lee (Author), Sunhee Lee (Author), Younho Lee (Author), Doona Song (Author), So-Hyeon Park (Author), Jieun Kim (Author), Wan Namkung (Author), Ikyon Kim (Author)
Format: Book
Published: MDPI AG, 2024-02-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Yechan Lee  |e author 
700 1 0 |a Sunhee Lee  |e author 
700 1 0 |a Younho Lee  |e author 
700 1 0 |a Doona Song  |e author 
700 1 0 |a So-Hyeon Park  |e author 
700 1 0 |a Jieun Kim  |e author 
700 1 0 |a Wan Namkung  |e author 
700 1 0 |a Ikyon Kim  |e author 
245 0 0 |a Anticancer Evaluation of Novel Benzofuran-Indole Hybrids as Epidermal Growth Factor Receptor Inhibitors against Non-Small-Cell Lung Cancer Cells 
260 |b MDPI AG,   |c 2024-02-01T00:00:00Z. 
500 |a 10.3390/ph17020231 
500 |a 1424-8247 
520 |a The epidermal growth factor receptor (EGFR), also known as ErbB1 and HER1, belongs to the receptor tyrosine kinase family. EGFR serves as the primary driver in non-small-cell lung cancer (NSCLC) and is a promising therapeutic target for NSCLC. In this study, we synthesized a novel chemical library based on a benzofuran-indole hybrid scaffold and identified <b>8aa</b> as a potent and selective EGFR inhibitor. Interestingly, <b>8aa</b> not only showed selective anticancer effects against NSCLC cell lines, PC9, and A549, but it also showed significant inhibitory effects against the double mutant L858R/T790M EGFR, which frequently occurs in NSCLC. In addition, in PC9 and A549 cells, <b>8aa</b> potently blocked the EGFR signaling pathway, cell viability, and cell migration. These findings suggest that <b>8aa</b>, a benzofuran-indole hybrid derivative, is a novel EGFR inhibitor that may be a potential candidate for the treatment of NSCLC patients with EGFR mutations. 
546 |a EN 
690 |a benzofuran 
690 |a indole 
690 |a hybrid structure 
690 |a NSCLC 
690 |a EGFR 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 17, Iss 2, p 231 (2024) 
787 0 |n https://www.mdpi.com/1424-8247/17/2/231 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/25afb50b92b64f0a88bdb9c7b8689080  |z Connect to this object online.