Abstract

Simple SummaryHead and neck squamous cell carcinoma (HNSCC), which arises from the oral epithelium, is one of the most common cancers worldwide. Despite excellent diagnosis and treatment improvements, the mortality rate associated with HNSCC is still extremely high. Current data suggest that dysregulation of exosomes and metabolic abnormalities are involved in the initiation and progression of HNSCC. Thus, approaches for targeting exosomes in the tumor microenvironment and metabolic reprogramming pathways represent potential therapeutic strategies. Moreover, some miRNAs are thought to have significant functions in regulating the progression of HNSCC. The present article aims to summarize the current knowledge concerning the important miRNAs in both exosomes and cancer metabolism, as well as discuss future perspectives regarding their future diagnostic potential and treatment recommendations.MicroRNAs (miRNAs) are endogenous small non-coding RNA molecules that negatively regulate gene expression by binding to target mRNAs. Deregulated miRNAs can act as either oncogenic miRNAs or tumor suppressor miRNAs in controlling proliferation, differentiation, apoptosis, metastasis, epithelial–mesenchymal transition, and immune responses, which are all involved in the carcinogenesis process of HNSCC. Recent findings have shown that metabolic reprogramming is an important hallmark of cancer, which is necessary for malignant transformation and tumor development. Some reprogrammed metabolisms are believed to be required for HNSCC against an unfavorable tumor microenvironment (TME). The TME is composed of various cell types embedded in the altered extracellular matrix, among which exosomes, secreted by cancer cells, are one of the most important factors. Tumor-derived exosomes reshape the tumor microenvironment and play a crucial role in cell-to-cell communication during HNSCC development. Exosomes encapsulate many biomolecules, including miRNAs, circulate in body fluids, and can transmit intercellular regulatory messages to nearby and distant sites, which indicates that exosomal miRNAs have the potential to become non-invasive biomarkers. This review aims to clarify the functions of diverse miRNAs in HNSCC metabolic reprogramming and tumor-derived exosomes. In addition, it also emphasizes the potential role of miRNA as a biomarker in the diagnosis, prognosis, and treatment of HNSCC cancer.

Highlights

  • Head and neck squamous cell carcinoma (HNSCC), which develops from the oral cavity, oropharynx, larynx, or hypopharynx, is the sixth most common malignancy in the world [1,2]

  • 1; PTEN, phosphatase and tensin homolog deleted on chromosome 10; SOCS1, suppressor of PD-L1, programmed death receptor ligand 1; PI3K, phosphoinositide 3-kinase; PIK3R1, phosphoinositide 3-kinase regulatory cytokine signaling 1; STAT6, signal transduction and transcriptional activator 6; TME, tumor microenvironment

  • Subunit 1; PTEN, phosphatase and tensin homolog deleted on chromosome 10; SOCS1, suppressor of cytokine signaling 1; STAT6, signal transduction and transcriptional activator 6; TME, tumor microenvironment

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Summary

Introduction

Head and neck squamous cell carcinoma (HNSCC), which develops from the oral cavity, oropharynx, larynx, or hypopharynx, is the sixth most common malignancy in the world [1,2]. Similar to miR-218, miR-340 has been reported to down-regulate in OSCC and work as a metabolic switch by regulating GLUT1 expression, leading to an increase in the glucose absorption rate and lactate secretion [34] Another miRNA of interest is miR-10a, which may play an oncogenic role in oral cancer by upregulating GLUT1 and increasing glucose metabolism [35]. Because there is no potential binding site of miR-10a in the 30 -UTR of GLUT1 mRNA, miR-10a may not be able to directly target GLUT1 [35] These data suggest that miR-10a may act as an upstream regulator of GLUT1 in OSCC for promoting cancer cell proliferation and glucose uptake. The reduction in glucose uptake will result in significant inhibition of proliferation, migration, and invasion Another case of a tumor-suppressive miRNA is miR-125b-5p, which has been found to be downregulated in laryngeal squamous cell carcinoma (LSCC) [37]. The expression level of PGE2 acts as a key mediator of miR-31-5p function, and it enhances cell motility by activating ERK-MMP9 signal transduction [39]

Exosomal miRNAs in HNSCC Tumor Microenvironment
Exosomal miRNAs
Exosomal miRNAs Crosstalk between HNSCC and TILs
Exosomal miRNAs Crosstalk between HNSCC and CAFs
Exosomal miRNAs Crosstalk between HNSCC and ECs
Clinical Implications of miRNA in HNSCC
Findings
Conclusions
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