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miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review

Oral squamous cell carcinoma (OSCC) is a malignancy of the oral cavity with poor prognosis. Dysregulation in glycolytic pathways involving glucose transporters (GLUT) has been implicated in poor prognosis. Furthermore, GLUT expression in cancer cells is regulated by several miRNAs. However, there is...

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Autores principales: R, Priyadharshini, Yuwanati, Monal, Sekaran, Saravanan, M, Senthilmurugan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605560/
https://www.ncbi.nlm.nih.gov/pubmed/37900425
http://dx.doi.org/10.7759/cureus.46057
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author R, Priyadharshini
Yuwanati, Monal
Sekaran, Saravanan
M, Senthilmurugan
author_facet R, Priyadharshini
Yuwanati, Monal
Sekaran, Saravanan
M, Senthilmurugan
author_sort R, Priyadharshini
collection PubMed
description Oral squamous cell carcinoma (OSCC) is a malignancy of the oral cavity with poor prognosis. Dysregulation in glycolytic pathways involving glucose transporters (GLUT) has been implicated in poor prognosis. Furthermore, GLUT expression in cancer cells is regulated by several miRNAs. However, there is a lack of data about miRNA involved in the regulation of GLUT in OSCC. The objective is to evaluate the role of miRNA in the regulation of GLUT in OSCC. Data sources include PubMed (MEDLINE), Scopus, and Web of Science. Studies evaluating the miRNA involved or associated with the regulation of GLUT in OSCC were included in the systematic review. Data pertaining to GLUT and associated miRNA expression were extracted from studies. Qualitative assessment was carried out for GLUT and miRNA. The Newcastle-Ottawa Scale was used for quality assessment. Ten study articles were included after analyzing 4675 papers. These studies evaluated the GLUT and miRNA expression between healthy and OSCC samples. There are variable expression patterns of GLUT in OSCC. Furthermore, it was dependent on miRNA. The GLUT1 and GLUT-3 were detected more frequently in OSCC, while no study reveals the expression of GLUT2, GLUT4, GLUT7, GLUT8, GLUT13, SGLT1, and SGLT2 with miRNA regulation. However, there was insufficient evidence on specific miRNA linked to GLUT1 or GLUT3 expression. There is evidence of the role of miRNA in the regulation of GLUT especially GLUT1 and GLUT3 in OSCC; however, a specific relation to miRNA was understudied. In the future, studies exploring a clearer understanding of the association between miRNA and the GLUT metabolic pathway in relation to OSCC are warranted. Furthermore, association of miRNA and GLUT with progression of disease, disease resistance, and prognosis is assessed for better treatment outcomes.
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spelling pubmed-106055602023-10-28 miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review R, Priyadharshini Yuwanati, Monal Sekaran, Saravanan M, Senthilmurugan Cureus Genetics Oral squamous cell carcinoma (OSCC) is a malignancy of the oral cavity with poor prognosis. Dysregulation in glycolytic pathways involving glucose transporters (GLUT) has been implicated in poor prognosis. Furthermore, GLUT expression in cancer cells is regulated by several miRNAs. However, there is a lack of data about miRNA involved in the regulation of GLUT in OSCC. The objective is to evaluate the role of miRNA in the regulation of GLUT in OSCC. Data sources include PubMed (MEDLINE), Scopus, and Web of Science. Studies evaluating the miRNA involved or associated with the regulation of GLUT in OSCC were included in the systematic review. Data pertaining to GLUT and associated miRNA expression were extracted from studies. Qualitative assessment was carried out for GLUT and miRNA. The Newcastle-Ottawa Scale was used for quality assessment. Ten study articles were included after analyzing 4675 papers. These studies evaluated the GLUT and miRNA expression between healthy and OSCC samples. There are variable expression patterns of GLUT in OSCC. Furthermore, it was dependent on miRNA. The GLUT1 and GLUT-3 were detected more frequently in OSCC, while no study reveals the expression of GLUT2, GLUT4, GLUT7, GLUT8, GLUT13, SGLT1, and SGLT2 with miRNA regulation. However, there was insufficient evidence on specific miRNA linked to GLUT1 or GLUT3 expression. There is evidence of the role of miRNA in the regulation of GLUT especially GLUT1 and GLUT3 in OSCC; however, a specific relation to miRNA was understudied. In the future, studies exploring a clearer understanding of the association between miRNA and the GLUT metabolic pathway in relation to OSCC are warranted. Furthermore, association of miRNA and GLUT with progression of disease, disease resistance, and prognosis is assessed for better treatment outcomes. Cureus 2023-09-27 /pmc/articles/PMC10605560/ /pubmed/37900425 http://dx.doi.org/10.7759/cureus.46057 Text en Copyright © 2023, R et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Genetics
R, Priyadharshini
Yuwanati, Monal
Sekaran, Saravanan
M, Senthilmurugan
miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title_full miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title_fullStr miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title_full_unstemmed miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title_short miRNA Associated With Glucose Transporters in Oral Squamous Cell Carcinoma: A Systematic Review
title_sort mirna associated with glucose transporters in oral squamous cell carcinoma: a systematic review
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605560/
https://www.ncbi.nlm.nih.gov/pubmed/37900425
http://dx.doi.org/10.7759/cureus.46057
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