Integrated Network Pharmacology Analysis and <i>In Vitro</i> Validation Revealed the Potential Active Components and Underlying Mechanistic Pathways of Herba Patriniae in Colorectal Cancer

Herba Patriniae (HP) are medicinal plants commonly used in colorectal cancer (CRC) patients. In this study, network pharmacology was used to predict the active components and key signaling pathways of HP in CRC. <i>Patrinia heterophylla</i>, one type of HP, was chosen for validation of t...

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Bibliographic Details
Main Authors: Huihai Yang, Man-Kit Cheung, Grace Gar-Lee Yue, Ping-Chung Leung, Chun-Kwok Wong, Clara Bik-San Lau
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/26/19/6032
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Summary:Herba Patriniae (HP) are medicinal plants commonly used in colorectal cancer (CRC) patients. In this study, network pharmacology was used to predict the active components and key signaling pathways of HP in CRC. <i>Patrinia heterophylla</i>, one type of HP, was chosen for validation of the network pharmacology analysis. The phytochemical profile of <i>Patrinia heterophylla</i> water extract (PHW) was determined by UHPLC-MS. MTT, RT-PCR, and Western blot assays were performed to evaluate the bioactivities of PHW in colon cancer cells. Results showed that 15 potentially active components of HP interacted with 28 putative targets of CRC in the compound–target network, of which asperglaucide had the highest degree. Furthermore, the ErbB signaling pathway was identified as the pathway mediated by HP with the most potential against CRC. Both RT-PCR and Western blot results showed that PHW significantly downregulated the mRNA and protein levels of EGFR, PI3K, and AKT in HCT116 cells. Asperglaucide, present in PHW, exhibited an anti-migratory effect in HCT116 cells, suggesting that it could be an active component of PHW in CRC treatment. In conclusion, this study has provided the first scientific evidence to support the use of PHW in CRC and paved the way for further research into the underlying mechanisms of PHW against CRC.
ISSN:1420-3049