miR-575/RIPK4 axis modulates cell cycle progression and proliferation by inactivating the Wnt/β-catenin signaling pathway through inhibiting RUNX1 in colon cancer
- 14 March 2024
- journal article
- research article
- Published by Springer Nature in Molecular and Cellular Biochemistry
- Vol. 479 (7) , 1747-1766
Abstract
Receptor interacting protein serine/threonine kinase 4 (RIPK4) is widely involved in human cancer development. Nevertheless, its role in colon cancer (COAD) has not been elucidated till now. Our research aimed at exploring the function and underlying molecular mechanism of RIPK4 in COAD progression. Through bioinformatic analyses and RT-qPCR, RIPK4 was discovered to be increased in COAD cells and tissues, and its high level predicted poor prognosis. Loss-of-function assays revealed that RIPK4 silencing suppressed COAD cell growth, induced cell cycle arrest, and enhanced cell apoptosis. In vivo experiments also proved that tumor growth was inhibited by silencing of RIPK4. Luciferase reporter assay validated that RIPK4 was targeted and negatively regulated by miR-575. Western blotting demonstrated that Wnt3a, phosphorylated (p)-GSK-3β, and cytoplasmic and nuclear β-catenin protein levels, β-catenin nuclear translocation, and Cyclin D1, CDK4, Cyclin E, and c-Myc protein levels were reduced by RIPK4 knockdown, which however was reversed by treatment with LiCl, the Wnt/β-catenin pathway activator. LiCl also offset the influence of RIPK4 knockdown on COAD cell growth, cell cycle process, and apoptosis. Finally, RIPK4 downregulation reduced RUNX1 level, which was upregulated in COAD and its high level predicted poor prognosis. RIPK4 is positively associated with RUNX1 in COAD. Overexpressing RUNX1 antagonized the suppression of RIPK4 knockdown on RUNX1, Wnt3a, p-GSK-3β, cytoplasmic β-catenin, nuclear β-catenin, Cyclin D1, CDK4, Cyclin E, and c-Myc levels. Collectively, miR-575/RIPK4 axis repressed COAD progression via inactivating the Wnt/β-catenin pathway through downregulating RUNX1.Keywords
Funding Information
- Health Commission of Hubei Province Scientific Research Project (WJ2019H129)
- Natural Science Foundation of Hubei Province (2019CFB640)
- Research Projects of Biomedical Center of Hubei Cancer Hospital (2022SWZX)
This publication has 57 references indexed in Scilit:
- Receptor interacting protein kinase 4 promotes cell proliferation, migration, and invasion in ovarian cancer via targeting protein kinase C deltaDrug Development Research, 2021
- Altered Expression of miR-575 in Glioma is Related to Tumor Cell Proliferation, Migration, and InvasionNeuroMolecular Medicine, 2021
- MicroRNA-575 regulates development of gastric cancer by targeting PTENBiomedicine & Pharmacotherapy, 2019
- Overexpression of miRNA-143 Inhibits Colon Cancer Cell Proliferation by Inhibiting Glucose UptakeArchives of Medical Research, 2018
- RIPK4 activity in keratinocytes is controlled by the SCFβ-TrCP ubiquitin ligase to maintain cortical actin organizationCellular and Molecular Life Sciences, 2018
- Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic ModalitiesCell, 2017
- RUNX1 contributes to higher-order chromatin organization and gene regulation in breast cancer cellsBiochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2016
- Specific miRNA Disease Biomarkers in Blood, Serum and Plasma: Challenges and ProspectsMolecular Diagnosis & Therapy, 2016
- The long non-coding RNA H19-derived miR-675 modulates human gastric cancer cell proliferation by targeting tumor suppressor RUNX1Biochemical and Biophysical Research Communications, 2014
- Tumor Metastasis: Molecular Insights and Evolving ParadigmsCell, 2011