MicroRNA-532-3p Modulates Colorectal Cancer Cell Proliferation and Invasion via Suppression of FOXM1

• Published in: Cancers Vol. 16; no. 17; p. 3061
• Main Authors: Mahajan, Ketakee, Das, Ani V, Alahari, Suresh K, Pothuraju, Ramesh, Nair, S Asha
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 02.09.2024
• Subjects: 3' Untranslated regions; Apoptosis; Breast cancer; Cancer; Cell cycle; Cell growth; Cell proliferation; Colorectal cancer; Colorectal carcinoma; Cyclin B1; Disease; Disease resistance; Drug resistance; E-cadherin; Forkhead protein; Gene regulation; Genes; Genomes; Kinases; Lymphoma; Medical prognosis; Metastases; Metastasis; MicroRNAs; miRNA; Older people; Phenotypes; Post-transcription; Promoters; Prostate; Proteins; Tumor cell lines; Tumor suppressor genes; Tumors; Vimentin; microRNA; colorectal cancer; FOXM1; metastasis
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers16173061

Colorectal cancer (CRC) is a heterogeneous disease and classified into various subtypes, among which transcriptional alterations result in CRC progression, metastasis, and drug resistance. Forkhead-box M1 (FOXM1) is a proliferation-associated transcription factor which is overexpressed in CRC and the mechanisms of regulation have been under investigation. Previously, we showed that FOXM1 binds to promoters of certain microRNAs. Database mining led to several microRNAs that might interact with 3'UTR. The interactions between shortlisted microRNAs and 3'UTR were quantitated by a dual-luciferase reporter assay. MicroRNA-532-3p interacted with the 3'UTR of the mRNA transcript most efficiently. MicroRNA-532-3p was ectopically overexpressed in colorectal cancer (CRC) cell lines, leading to reduced transcript and protein levels of and , a direct transcriptional target of FOXM1. Further, a clonogenic assay was conducted in overexpressed miR-532-3p CRC cells that revealed a decline in the ability of cells to form colonies and a reduction in migratory and invading potential. These alterations were reinforced at molecular levels by the altered transcript and protein levels of the conventional EMT markers E-cadherin and vimentin. Overall, this study identifies the regulation of by microRNA-532-3p via its interaction with 3'UTR, resulting in the suppression of proliferation, migration, and invasion, suggesting its role as a tumor suppressor in CRC.