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Metabolomics and integrated network pharmacology analysis reveal SNKAF decoction suppresses cell proliferation and induced cell apoptisis in hepatocellular carcinoma via PI3K/Akt/P53/FoxO signaling axis.

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机构: [1]The First Affiliated Hospital of Guangzhou University of Chinese Medicine,Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong,People’s Republic of China [2]The Research Center for Integrative Medicine,School of Basic Medical Sciences, Guangzhou University of Chinese Medicine,Guangzhou 510006, Guangdong, People’s Republic of China [3]Departmentof Nephrology, Huizhou Municipal Central Hospital, Huizhou 510006,Guangdong, People’s Republic of China [4]Department of Pathology, The FirstAffiliated Hospital of Sun Yat Sen University, Guangzhou 510080, Guangdong,People’s Republic of China
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关键词: Hepatocellular carcinoma Network pharmacology Metabolomic analysis SNKAF decoction PI3K/Akt/P53/FoxO signaling pathway axis

摘要:
There is no comprehensive treatment method for hepatocellular carcinoma (HCC); hence, research and development are still focused on systemic therapies, including drugs. Sinikangai fang (SNKAF) decoction, a classic Chinese herbal prescription, has been widely used to treat liver cancer. However, there is no research on its core active component and target.Mouse models were established to measure the anticancer effect of SNKAF decoction on HCC. Further, we investigated the effect of SNKAF decoction on inhibition of hepatoma cells proliferation using cell viability, cloning and invasion assays in vitro. The components of SNKAF were collected from the Traditional Chinese Medicine Systems Pharmacology (TCMSP) database and TCM@Taiwan database. Metabolomic analysis was used to identify the potential genes and pathways in HCC treated with SNKAF decoction. Then, the expression of phosphoinositide 3-kinase (PI3K), Akt, P53, FoxO proteins of the potential signal pathways were detected using Western blot.The animal experiments showed that SNKAF decoction inhibited tumor growth (P < 0.05) and induced no weight loss in the mice. In vitro data showed that HCCLM3 and MHCC97H cell proliferation was inhibited by SNKAF serum in a time- and concentration dependent manner. Further combined analysis network pharmacology with metabonomics showed that 217 target genes overlapped. The core target genes included BCL2, MCL1, Myc, PTEN, gsk3b, CASP9, CREB1, MDM2, pt53 and CCND1. Cancer-associated pathways were largely involved in SNKAF mechanisms, including P53, FoxO, and PI3K/Akt signaling pathways, which are closely related to induced-tumor cell apoptosis. In addition, Western bolt verified that 10% SNKAF serum significantly affected the main proteins of PI3K/Akt/P53/FoxO signaling pathway in both cell lines.SNKAF decoction-containing serum inhibited HCCLM3 and MHCC97H cell proliferation, migration, invasion, and induced-tumor cell apoptosis in-vivo. We confirmed that SNKAF decoction is a promising alternative treatments for HCC patients.© 2022. The Author(s).

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出版当年[2021]版:
大类 | 3 区 医学
小类 | 2 区 全科医学与补充医学 3 区 药学
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 全科医学与补充医学 2 区 药学
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出版当年[2020]版:
Q1 PHARMACOLOGY & PHARMACY Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE
最新[2023]版:
Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Q1 PHARMACOLOGY & PHARMACY

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第一作者机构: [1]The First Affiliated Hospital of Guangzhou University of Chinese Medicine,Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong,People’s Republic of China
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