PAK1号
结直肠癌
自噬
细胞凋亡
癌症研究
癌症
激酶
恶性肿瘤
癌细胞
生物
化学
医学
细胞生物学
内科学
生物化学
作者
Yi Liu,Yuling Zou,Yongxiong Huang,Siwei Chen,Lan Zhang
标识
DOI:10.1002/cmdc.202300114
摘要
Abstract Colorectal cancer (CRC) is a common malignancy of the gastrointestinal tract, often accompanied by poor prognosis and high incidence and mortality. p21 activated kinases (PAKs) have been used as therapeutic targets because of their central role in many oncogenic signaling networks. By exploring tumor databases, we found that PAK1 overexpression is associated with poor prognosis in colorectal cancer, and therefore, PAK1‐targeted inhibition is a new potential therapeutic strategy for colorectal cancer. We identified that Balanol (compound 6 , DB04098) can effectively target PAK1 by high‐throughput virtual screening. In vitro , compound 6 exhibited favorable PAK1 inhibition with potent anti‐proliferative and anti‐migration activity in SW480 cells. Additionally, we also found that compound 6 induced apoptosis and cytoprotective autophagy in SW480 cells. Together, these results indicate that compound 6 is a potential novel PAK1 inhibitor, which would be utilized as a candidate compound for future CRC treatment.
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