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Roles of microRNAs in Regulating Cancer Stemness in Head and Neck Cancers

期刊

CANCERS
卷 13, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13071742

关键词

microRNA; cancer stem cell; stemness; head and neck squamous cell carcinoma

类别

资金

  1. Yen Tjing Ling Medical Foundation in Taiwan
  2. Cancer Progression Research Center, National Yang Ming Chiao Tung University, from the Featured Areas Research Center Program
  3. Ministry of Science and Technology [109-2320-B-010-021, MOST 109-2636-B-038-001, MOST 110-2636-B-038-005]
  4. Taipei Medical University [TMU108-AE1-B25]
  5. Yen Tjing Ling Medical Foundation [CI-109-11]
  6. Ministry of Health and Welfare, Center of Excellence for Cancer Research [MOHW107-TDU-B-211-114019, 109 CRC-T208, 110 CRC-T208]

向作者/读者索取更多资源

Head and neck squamous cell carcinomas (HNSCCs) are heterogeneous malignancies with cancer stem cells (CSCs) playing vital roles in tumor progression, metastasis, and therapeutic resistance. MicroRNAs (miRNAs) regulate CSC features in HNSCC by modulating tumor microenvironment and signaling pathways, offering potential therapeutic applications.
Simple Summary Head and neck squamous cell carcinomas (HNSCCs) are highly heterogeneous human malignancies associated with genetic and environmental factors. In HNSCCs, cancer stem cells (CSCs) provide the plasticity for cancer cell progression, metastasis, therapeutic resistance, and recurrence. During carcinogenesis, microRNAs (miRNAs) play important roles in regulating the maintenance and acquisition of cancer stem cell features. Therefore, in this review, we summarize the roles of miRNAs in regulating the cancer stemness of HNSCCs to provide potential therapeutic applications. Head and neck squamous cell carcinomas (HNSCCs) are epithelial malignancies with 5-year overall survival rates of approximately 40-50%. Emerging evidence indicates that a small population of cells in HNSCC patients, named cancer stem cells (CSCs), play vital roles in the processes of tumor initiation, progression, metastasis, immune evasion, chemo-/radioresistance, and recurrence. The acquisition of stem-like properties of cancer cells further provides cellular plasticity for stress adaptation and contributes to therapeutic resistance, resulting in a worse clinical outcome. Thus, targeting cancer stemness is fundamental for cancer treatment. MicroRNAs (miRNAs) are known to regulate stem cell features in the development and tissue regeneration through a miRNA-target interactive network. In HNSCCs, miRNAs act as tumor suppressors and/or oncogenes to modulate cancer stemness and therapeutic efficacy by regulating the CSC-specific tumor microenvironment (TME) and signaling pathways, such as epithelial-to-mesenchymal transition (EMT), Wnt/beta-catenin signaling, and epidermal growth factor receptor (EGFR) or insulin-like growth factor 1 receptor (IGF1R) signaling pathways. Owing to a deeper understanding of disease-relevant miRNAs and advances in in vivo delivery systems, the administration of miRNA-based therapeutics is feasible and safe in humans, with encouraging efficacy results in early-phase clinical trials. In this review, we summarize the present findings to better understand the mechanical actions of miRNAs in maintaining CSCs and acquiring the stem-like features of cancer cells during HNSCC pathogenesis.

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