Phytomedicine : international journal of phytotherapy and phytopharmacology · 2025
Fuzheng YiLiu decoction promote colorectal cancer apoptosis and reduce its proliferation via IGF2/IGF1R/PI3K/AKT pathway.
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Wei Yu, Jiang Zhangyu, Song Changlin, Qiao Yuanyuan, Wang Xianzhe, Ma Wenhui, Wang Tao, Xu Yuting, Wang Fei, Xiong Wenjun, Wang Wei
Аннотация
BACKGROUND: Colorectal cancer (CRC) is one of the most common cancers, with high incidence and mortality rates. This Traditional Chinese Medicine (TCM) FuZheng YiLiu (FZYL) decoction is widely used in the treatment of CRC at the First Affiliated Hospital of Guangzhou University of Chinese Medicine. However, its mechanism of action remains unclear.
AIM: To investigate the therapeutic effects and mechanisms of FZYL against CRC.
METHODS: BALB/c nu mice bearing orthotopic colon tumors were treated with FZYL. Tumor burden, organ function, histology, and serum metabolites were evaluated. UPLCHRMS identified FZYL components, and network pharmacology predicted key targets and pathways. In vitro assays assessed proliferation and apoptosis. PCR array, RT-qPCR, IHC, and WB validated molecular mechanisms. Molecular docking and dynamics examined interactions between major FZYL compounds and IGF1R, PIK3CA, AKT1.
RESULTS: FZYL reduced tumor growth and angiogenesis, alleviated colitis, and showed no liver or kidney toxicity. Metabolomics and network pharmacology highlighted PI3K/AKT signaling, with IGF2/IGF1R and RAS identified as key nodes. FZYL downregulated IGF2, IGF1R, p-PI3K, p-AKT, Ki67, and PCNA, while upregulating Caspase3, BCL2, and Bax. In vitro, FZYL inhibited SW620 cell proliferation and induced apoptosis via the IGF2/IGF1R/PI3K/AKT pathway. Docking and dynamics confirmed strong binding between FZYL compounds and IGF1R/PIK3CA/AKT1.
CONCLUSION: FZYL may inhibit CRC proliferation and promote apoptosis by suppressing the IGF2/IGF1R/PI3K/AKT pathway, potentially slowing down the progression of colorectal cancer.
AIM: To investigate the therapeutic effects and mechanisms of FZYL against CRC.
METHODS: BALB/c nu mice bearing orthotopic colon tumors were treated with FZYL. Tumor burden, organ function, histology, and serum metabolites were evaluated. UPLCHRMS identified FZYL components, and network pharmacology predicted key targets and pathways. In vitro assays assessed proliferation and apoptosis. PCR array, RT-qPCR, IHC, and WB validated molecular mechanisms. Molecular docking and dynamics examined interactions between major FZYL compounds and IGF1R, PIK3CA, AKT1.
RESULTS: FZYL reduced tumor growth and angiogenesis, alleviated colitis, and showed no liver or kidney toxicity. Metabolomics and network pharmacology highlighted PI3K/AKT signaling, with IGF2/IGF1R and RAS identified as key nodes. FZYL downregulated IGF2, IGF1R, p-PI3K, p-AKT, Ki67, and PCNA, while upregulating Caspase3, BCL2, and Bax. In vitro, FZYL inhibited SW620 cell proliferation and induced apoptosis via the IGF2/IGF1R/PI3K/AKT pathway. Docking and dynamics confirmed strong binding between FZYL compounds and IGF1R/PIK3CA/AKT1.
CONCLUSION: FZYL may inhibit CRC proliferation and promote apoptosis by suppressing the IGF2/IGF1R/PI3K/AKT pathway, potentially slowing down the progression of colorectal cancer.
Предметные рубрики MeSH
AnimalsApoptosisProto-Oncogene Proteins c-aktMice, Inbred BALB CCell ProliferationDrugs, Chinese HerbalColorectal NeoplasmsPhosphatidylinositol 3-KinasesInsulin-Like Growth Factor IISignal TransductionHumansMiceCell Line, TumorMice, NudeReceptor, IGF Type 1Molecular Docking SimulationMaleAntineoplastic Agents, Phytogenic