Traditional Chinese medicine Bu-Shen-Jian-Pi-Fang attenuates glycolysis and immune escape in clear cell renal cell carcinoma: results based on network pharmacology

Author:

Zheng Jinzhou1,Xu Wenhao2,Liu Wangrui3ORCID,Tang Haijia4,Lu Jingen1,Yu Kui1,Song Xiaoyun1,Li Feng1,Wang Yu1,Wang Rui1,Chen Lili1,Zhang Hailiang2,Qiu Yunhua1,Wei Gaomeng3,Zhou Xiqiu1,Yang Jianfeng1ORCID

Affiliation:

1. Department of Surgery, PuDong branch of Longhua Hospital, Shanghai University of Traditional Chinese Medicine, 1000 Shangnan road, Shanghai 200126, China

2. Department of Urology, Fudan University Shanghai Cancer Center, Shanghai 200030, China

3. Department of Urology, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi 533000, China

4. Department of Integrated Medicine, Nanjing University of Chinese Medicine, Nanjing 210000, China

Abstract

Abstract Clear cell renal cell carcinoma (ccRCC) is the most common malignant type of kidney cancer. The present study aims to explore the underlying mechanism and potential targets of the traditional Chinese medicine Bu-Shen-Jian-Pi-Fang (BSJPF) in the treatment of ccRCC based on network pharmacology. After obtaining the complete composition information for BSJPF from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform, we analyzed its chemical composition and molecular targets and then established a pharmacological interaction network. Twenty-four significantly differentially expressed genes and nine pathways mainly related to tumor proliferation were identified and screened. Functional enrichment analysis indicated that the potential targets might be significantly involved in glycolysis and the HIF-1 signaling pathway. To further confirm the effect of BSJPF on ccRCC cell proliferation, a BALB/c xenograft mouse model was constructed. Potential targets involved in regulating glycolysis and the tumor immune microenvironment were evaluated using RT-qPCR. VEGF-A expression levels were markedly decreased, and heparin binding-EGF expression was increased in the BSJPF group. BSJPF also inhibited tumor proliferation by enhancing GLUT1- and LDHA-related glycolysis and the expression of the immune checkpoint molecules PD-L1 and CTLA-4, thereby altering the immune-rejection status of the tumor microenvironment. In summary, the present study demonstrated that the mechanism of BSJPF involves multiple targets and signaling pathways related to tumorigenesis and glycolysis metabolism in ccRCC. Our research provides a novel theoretical basis for the treatment of tumors with traditional Chinese medicine and new strategies for immunotherapy in ccRCC patients.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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