Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula

被引:4
作者
Zhang, Zexin [1 ]
Lin, Siqi [2 ]
Liu, Zifeng [2 ]
Han, Jun [3 ]
Li, Jing [4 ]
Yu, Yi [4 ]
机构
[1] Guangzhou Univ Chinese Med, Clin Med Coll 1, Guangzhou 510405, Peoples R China
[2] Guangzhou Univ Chinese Med, Clin Med Coll 2, Guangzhou 510405, Peoples R China
[3] Beijing Tcmages Pharmaceut Co Ltd, Natl & Local Joint Engn Res Ctr Key Technol Chine, Beijing 101301, Peoples R China
[4] Hunan Univ Chinese Med, Affiliated Hosp 1, Changsha 410000, Peoples R China
关键词
IL-3; EXPRESSION; GROWTH; CELLS;
D O I
10.1155/2022/7998664
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background. Tao-He-Cheng-Qi Formula (THCQF) is a traditional Chinese medicine that has been proven to have antitumor effects. The aim of this study was to elucidate the molecular targets and mechanisms of THCQF against colon cancer and construct a prognostic model based on network pharmacology, bioinformatics analysis, and in vitro experiments. Methods. Potential THCQF compounds and targets were retrieved from the Traditional Chinese Medicine Systems Pharmacology and Bioinformatics Analysis Tool for Molecular Mechanism of Traditional Chinese Medicine databases. Differentially expressed genes for colon cancer were screened in The Cancer Genome Atlas and Gene Expression Omnibus databases. The anticolon cancer mechanisms of THCQF were explored using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Molecular docking simulations and molecular dynamics analysis were used to evaluate the binding between target proteins and active compounds. Finally, the identified compounds were used to treat colon cancer cells from the HCT116 cell line, and expression of mRNA and protein after relevant posttreatment were tested using real-time polymerase chain reaction and western blotting. Results. A total of 27 anticolon cancer targets of THCQF were selected, among which four genes (CCNB1, CCNA2, IL1A, and MMP3) were shown to effectively predict patient outcomes in a prognostic colon cancer model. GO and KEGG enrichment analyses indicated that the activity against colon cancer of THCQF was associated with the interleukin (IL)-4 and IL-3 signaling pathways. Two compounds in THCQF, aloe emodin (AE) and quercetin (QR), were shown to efficiently bind to cyclin B1, the protein encoded by CCNB1. Finally, incubation of HCT116 cells with AE and QR significantly decreased CCNB1 mRNA expression and cyclin B1 levels. Conclusions. Taken together, the results indicate that AE and QR are the pivotal active compounds of THCQF, and CCNB1 is the main molecular target through which THCQF exerts its anticolon cancer effects. The study findings provide insight for studies investigating the anticancer effects of other traditional Chinese medicines.
引用
收藏
页数:22
相关论文
共 54 条
[1]   Emodin, a natural anthraquinone, suppresses liver cancer in vitro and in vivo by regulating VEGFR2 and miR-34a [J].
Bai, Jianguo ;
Wu, Jianfei ;
Tang, Ruifeng ;
Sun, Chao ;
Ji, Junwei ;
Yin, Zhaolin ;
Ma, Guangjun ;
Yang, Wei .
INVESTIGATIONAL NEW DRUGS, 2020, 38 (02) :229-245
[2]   Pathophysiology, clinical presentation, and management of colon cancer [J].
Cappell, Mitchell S. .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2008, 37 (01) :1-+
[3]   HnRNPR-CCNB1/CENPF axis contributes to gastric cancer proliferation and metastasis [J].
Chen, Er-Bao ;
Qin, Xuan ;
Peng, Ke ;
Li, Qian ;
Tang, Cheng ;
Wei, Yi-Chou ;
Yu, Shan ;
Gan, Lu ;
Liu, Tian-Shu .
AGING-US, 2019, 11 (18) :7473-7491
[4]   Aloe-Emodin Induces Endoplasmic Reticulum Stress-Dependent Apoptosis in Colorectal Cancer Cells [J].
Cheng, Chunsheng ;
Dong, Weiguo .
MEDICAL SCIENCE MONITOR, 2018, 24 :6331-6339
[5]   IL-3 affects endothelial cell-mediated smooth muscle cell recruitment by increasing TGFβ activity:: potential role in tumor vessel stabilization [J].
Dentelli, P ;
Rosso, A ;
Calvi, C ;
Ghiringhello, B ;
Garbarino, G ;
Camussi, G ;
Pegoraro, L ;
Brizzi, MF .
ONCOGENE, 2004, 23 (09) :1681-1692
[6]   GM-CSF, IL-3, and IL-5 Family of Cytokines: Regulators of Inflammation [J].
Dougan, Michael ;
Dranoff, Glenn ;
Dougan, Stephanie K. .
IMMUNITY, 2019, 50 (04) :796-811
[7]   Enhanced breast cancer progression by mutant p53 is inhibited by the circular RNA circ-Ccnb1 [J].
Fang, Ling ;
Du, William W. ;
Lyu, Juanjuan ;
Dong, Jun ;
Zhang, Chao ;
Yang, Weining ;
He, Alina ;
Kwok, Yat Sze Sheila ;
Ma, Jian ;
Wu, Nan ;
Li, Feiya ;
Awan, Faryal Mehwish ;
He, Chengyan ;
Yang, Bing L. ;
Peng, Chun ;
MacKay, Helen J. ;
Yee, Albert J. ;
Yang, Burton B. .
CELL DEATH AND DIFFERENTIATION, 2018, 25 (12) :2195-2208
[8]   Colorectal Cancer: National and International Perspective on the Burden of Disease and Public Health Impact [J].
Gellad, Ziad F. ;
Provenzale, Dawn .
GASTROENTEROLOGY, 2010, 138 (06) :2177-2190
[9]   Growth inhibitory effects of gastric cancer cells with an increase in S phase and alkaline phosphatase activity repression by aloe-emodin [J].
Guo, Junming ;
Xiao, Bingxiu ;
Zhang, Shun ;
Liu, Donghai ;
Liao, Yiping ;
Sun, Qian .
CANCER BIOLOGY & THERAPY, 2007, 6 (01) :85-88
[10]   Cyclin B1 acts as a tumor microenvironment-related cancer promoter and prognostic biomarker in hepatocellular carcinoma [J].
Hou, Yangming ;
Wang, Xin ;
Wang, Junwei ;
Sun, Xuemei ;
Liu, Xinbo ;
Hu, Han ;
Fan, Wenzhe ;
Zhang, Xinchen ;
Wu, Dequan .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2021, 49 (05)