» Articles » PMID: 37773732

Inhibits the Growth and Metastasis of Liver Cancer by Downregulating MiR-9-5p and Upregulating PDK4

Overview
Specialties Oncology
Pharmacology
Date 2023 Sep 29
PMID 37773732
Authors
Affiliations
Soon will be listed here.
Abstract

A growing number of studies have suggested that traditional Chinese medicine (TCM) plays an essential role in the development and occurrence of liver cancer. However, the function of Ruangan Lidan decoction (RLD) in liver cancer are not yet adequately identified and manifested, which attracted our attention. The key genes related to liver cancer and RLD and the upstream miRNAs of PDK4 were obtained based on bioinformatics analysis, followed by verification of the targeting relationship between miR-9-5p and PDK4. Next, Huh7 cells were treated with RLD to detect cell proliferation, colony formation, migration, invasion, and apoptosis by multiple assays with gain- and loss-of-function experiments. Moreover, subcutaneous transplanted tumor model and lung metastasis model of liver cancer in nude mice were established to further verify the functional role of RLD in liver cancer growth and metastasis via miR-9-5p/PDK4 axis. Bioinformatics analysis found that PDK4 and miR-9-5p were related to liver cancer, and PDK4 may be a downstream regulator of RLD. miR-9-5p could target and inhibit PDK4. In vitro cell experiments demonstrated that RLD suppressed liver cancer cell proliferation, invasion and migration, and promoted apoptosis by inhibiting miR-9-5p expression and promoting PDK4 expression. In vivo animal experiments further confirmed that RLD inhibited liver cancer growth and metastasis via upregulation of miR-9-5p-dependent PDK4. RLD downregulated miR-9-5p and upregulated PDK4 to inhibit the proliferation, migration, invasion, and induce apoptosis, thereby suppressing the growth and metastasis of liver cancer, highlighting a potential novel target for treatment of liver cancer.

Citing Articles

Invasion and metastasis in cancer: molecular insights and therapeutic targets.

Li Y, Liu F, Cai Q, Deng L, OuYang Q, Zhang X Signal Transduct Target Ther. 2025; 10(1):57.

PMID: 39979279 PMC: 11842613. DOI: 10.1038/s41392-025-02148-4.


Identification and analysis of key genes related to efferocytosis in colorectal cancer.

Zhang S, Jiang Y, Shi L, Wei T, Lai Z, Feng X BMC Med Genomics. 2024; 17(1):198.

PMID: 39107816 PMC: 11304617. DOI: 10.1186/s12920-024-01967-8.


Abrogating PDK4 activates autophagy-dependent ferroptosis in breast cancer via ASK1/JNK pathway.

Shi W, Wang J, Chen J, Jin X, Wang Y, Yang L J Cancer Res Clin Oncol. 2024; 150(4):218.

PMID: 38678126 PMC: 11055733. DOI: 10.1007/s00432-024-05748-9.

References
1.
Si T, Ning X, Zhao H, Zhang M, Huang P, Hu Z . microRNA-9-5p regulates the mitochondrial function of hepatocellular carcinoma cells through suppressing PDK4. Cancer Gene Ther. 2020; 28(6):706-718. DOI: 10.1038/s41417-020-00253-w. View

2.
Pei T, Yan M, Huang Y, Wei Y, Martin C, Zhao Q . Specific Flavonoids and Their Biosynthetic Pathway in . Front Plant Sci. 2022; 13:866282. PMC: 8928390. DOI: 10.3389/fpls.2022.866282. View

3.
Linck-Paulus L, Hellerbrand C, Bosserhoff A, Dietrich P . Dissimilar Appearances Are Deceptive-Common microRNAs and Therapeutic Strategies in Liver Cancer and Melanoma. Cells. 2020; 9(1). PMC: 7017070. DOI: 10.3390/cells9010114. View

4.
Yang C, Wang S, Ruan H, Li B, Cheng Z, He J . Downregulation of PDK4 Increases Lipogenesis and Associates with Poor Prognosis in Hepatocellular Carcinoma. J Cancer. 2019; 10(4):918-926. PMC: 6400816. DOI: 10.7150/jca.27226. View

5.
Dai M, Yang Y, Guo W, Wang F, Xiao G, Li Y . Addition and Subtraction Theory of TCM Using Xiao-Chaihu-Decoction and Naturopathy in Predicting Survival Outcomes of Primary Liver Cancer Patients: A Prospective Cohort Study. Evid Based Complement Alternat Med. 2016; 2016:4723530. PMC: 5098078. DOI: 10.1155/2016/4723530. View