Author:
Xue Zhong,Zhang Fan,Xu Shaohua,Chen Minyong,Wang Mingzuo,Wang Ming,Ke Fayong,Chen Zhaoshuo,Zhang Mingji
Abstract
Hepatocellular carcinoma is one of the cancers that kill people in the global population. Icaritin, a small molecule drug approved by NMPA, has demonstrated potential anti-HCC effects. However, its underlying molecular mechanisms remain unclear. We employed a multi-omics approach in this study, including pharmaco-omics and proteomics, to look into the Icaritin’s possible molecular targets and workings in the therapy of HCC. Through pharmaco-omics analysis, we identified ten putative target genes of Icaritin, including FYN. The relationship between Icaritin and these target genes, particularly FYN, was further validated through in vitro and in vivo experiments. The outcomes revealed that Icaritin may exert its anti-HCC effects through modulating the FYN gene, highlighting the importance of multi-omics approaches in drug discovery research. This research gives valuable insights regarding the therapeutic potential of Icaritin against HCC and its possible molecular mechanisms.
Subject
Pharmacology (medical),Pharmacology
Reference38 articles.
1. Hepatobiliary cancers, version 2.2021, NCCN clinical practice guidelines in oncology;Benson;J. Natl. Compr. Canc Netw.,2021
2. SwissTargetPrediction: Updated data and new features for efficient prediction of protein targets of small molecules;Daina;Nucleic acids Res.,2019
3. Posadas, SRC family kinase FYN promotes the neuroendocrine phenotype and visceral metastasis in advanced prostate cancer;Gururajan;Oncotarget,2015
4. Network pharmacology: A rosetta stone for traditional Chinese medicine;Hao;Drug Dev. Res.,2014
5. Gromacs 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation;Hess;J. Chem. Theory Comput.,2008
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