miR-34a-5p functions as a tumor suppressor in head and neck squamous cell cancer progression by targeting Flotillin-2.

Int J Biol Sci

Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, 136 Hanzhong Road, Nanjing 210029, Jiangsu Province, China.

Published: December 2021

AI Article Synopsis

  • Advances in treatment for head and neck squamous cell cancer (HNSCC) have not significantly improved patient survival rates, making research into new therapeutic avenues critical.
  • The study focuses on the role of microRNA miR-34a-5p, which is downregulated in various tumors, including HNSCC, and investigates its impact on tumor progression.
  • Findings indicate that miR-34a-5p acts as a tumor suppressor by limiting cell proliferation and invasion, and it does so by targeting flotillin-2 (FLOT-2) and activating the MEK/ERK1/2 signaling pathway, suggesting potential for new treatment strategies.

Article Abstract

While a number of therapeutic advances have been made in recent years, the overall survival of patients with head and neck squamous cell cancer (HNSCC) remains poor. MicroRNAs (miRNAs) are key drivers of oncogenic progression, with miR-34a-5p downregulation having been observed in many different tumor types. Here, we assessed the link between miR-34a-5p and HNSCC progression and the mechanistic basis for this relationship. Levels of miR-34a-5p in HNSCC tumors and cell lines were assessed via qPCR, after which we explored the functional importance of this miRNA in this oncogenic setting. Through luciferase reporter assays, the ability of miR-34a-5p to regulate flotillin-2 (FLOT-2) was further clarified. Overall, these analyses revealed that HNSCC tumors and cells exhibited marked miR-34a-5p downregulation that was linked to the progression of this tumor type. At a functional level, miR-34a-5p constrained the proliferation, migratory/invasive activity, and epithelial-mesenchymal transition induction in HNSCC cells. At the mechanistic level, miR-34a-5p was found to suppress FLOT-2 expression and to activate the MEK/ERK1/2 pathway. Overall, these results suggest that miR-34a-5p can function as a tumor suppressor miRNA in HNSCC owing to its ability to target FLOT-2, highlighting the promise of targeting this regulatory axis to treat HNSCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579463PMC
http://dx.doi.org/10.7150/ijbs.64851DOI Listing

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