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

被引:20
|
作者
Guo, Wei [1 ]
Yao, Xiaohui [2 ]
Lan, Siyuan [2 ]
Zhang, Chi [1 ]
Li, Hanhan [1 ]
Chen, Zhuangzhong [1 ]
Yu, Ling [1 ]
Liu, Guanxian [3 ]
Lin, Yuan [4 ]
Liu, Shan [1 ]
Chen, Hanrui [1 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Res Ctr Integrat Med, Sch Basic Med Sci, Guangzhou 510006, Guangdong, Peoples R China
[3] Huizhou Municipal Cent Hosp, Dept Nephrol, Huizhou 510006, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Dept Pathol, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
关键词
Hepatocellular carcinoma; Network pharmacology; Metabolomic analysis; SNKAF decoction; PI3K; Akt; P53; FoxO signaling pathway axis; FLIGHT MASS-SPECTROMETRY; CANCER; SORAFENIB; APOPTOSIS; MEDICINE;
D O I
10.1186/s13020-022-00628-1
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background 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. Methods 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. Results 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. Conclusion 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.
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页数:19
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