The role of miRNAs in laryngeal cancer pathogenesis and therapeutic resistance – A focus on signaling pathways interplay

Laryngeal cancer (LC)is the malignancy of the larynx (voice box). The majority of LC are squamous cell carcinomas. Many risk factors were reported to be associated with LC as tobacco use, obesity, alcohol intake, human papillomavirus (HPV) infection, and asbestos exposure. Besides, epigenetics as no...

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Veröffentlicht in:Pathology, research and practice research and practice, 2023-06, Vol.246, p.154510-154510, Article 154510
Hauptverfasser: Hegazy, Maghawry, Elkady, Mohamed A., Yehia, Amr Mohamed, Elsakka, Elsayed G.E., Abulsoud, Ahmed I., Abdelmaksoud, Nourhan M., Elshafei, Ahmed, Abdelghany, Tamer M., Elkhawaga, Samy Y., Ismail, Ahmed, Mokhtar, Mahmoud Mohamed, El-Mahdy, Hesham A., Doghish, Ahmed S.
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Sprache:eng
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Zusammenfassung:Laryngeal cancer (LC)is the malignancy of the larynx (voice box). The majority of LC are squamous cell carcinomas. Many risk factors were reported to be associated with LC as tobacco use, obesity, alcohol intake, human papillomavirus (HPV) infection, and asbestos exposure. Besides, epigenetics as non-coding nucleic acids also have a great role in LC. miRNAs are short nucleic acid molecules that can modulate multiple cellular processes by regulating the expression of their genes. Therefore, LC progression, apoptosis evasions, initiation, EMT, and angiogenesis are associated with dysregulated miRNA expressions. miRNAs also could have some vital signaling pathways such as mTOR/P-gp, Wnt/-catenin signaling, JAK/STAT, KRAS, and EGF. Besides, miRNAs also have a role in the modulation of LC response to different therapeutic modalities. In this review, we have provided a comprehensive and updated overview highlighting the microRNAs biogenesis, general biological functions, regulatory mechanisms, and signaling dysfunction in LC carcinogenesis, in addition to their clinical potential for LC diagnosis, prognosis, and chemotherapeutics response implications.
ISSN:0344-0338
1618-0631
DOI:10.1016/j.prp.2023.154510