| Literature DB >> 32728182 |
Wei Zhou1, Jiarui Wu2, Jingyuan Zhang1, Xinkui Liu1, Siyu Guo1, ShanShan Jia1, Xiaomeng Zhang1, Yingli Zhu1, Miaomiao Wang1.
Abstract
Compound Kushen injection (CKI), a medicine in widespread clinical use in China, has proven therapeutic effects on cancer. However, few molecular mechanism analyses have been carried out. To address this problem, bioinformatics approaches combining weighted gene co-expression network analysis with network pharmacology methods were undertaken to elucidate the underlying molecular mechanisms of CKI in the treatment of esophageal cancer (ESCA). First, the key gene modules related to the clinical traits of ESCA were analysed by WCGNA. Based on the results, the hub genes related to CKI treatment for ESCA were explored through network pharmacology. Molecular docking simulation was performed to recognize the binding activity of hub genes with CKI compounds. The results showed that the potential hub targets, including EGFR, ErbB2, CCND1 and IGF1R, are therapeutic targets of CKI for the treatment of ESCA. Moreover, these targets were significantly enriched in many pathways related to cancer and signalling pathways, such as the PI3K-Akt signalling pathway and ErbB signalling pathway. In conclusion, this research partially highlighted the molecular mechanism of CKI in the treatment of ESCA, offering great potential in the identification of the effective compounds in CKI and biomarkers for ESCA treatment.Entities:
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Year: 2020 PMID: 32728182 PMCID: PMC7391752 DOI: 10.1038/s41598-020-69708-2
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379