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Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker
INTRODUCTION: MicroRNAs (miRs) are a group of endogenous, non-coding, 18–24 nucleotide length single-strand RNAs. These molecules mediate the gene expression and are involved in regulating diverse cellular biological processes, i.e. cell cycle, differentiation, and apoptosis. Aberrant miR expression...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607090/ https://www.ncbi.nlm.nih.gov/pubmed/34319042 http://dx.doi.org/10.31557/APJCP.2021.22.7.2185 |
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author | Bolandparva, Farzaneh Hashemi Nasab, Mahboobeh Sadat Mohamadnia, Abdolreza Garajei, Ata Farhadi Nasab, Abdollah Bahrami, Naghmeh |
author_facet | Bolandparva, Farzaneh Hashemi Nasab, Mahboobeh Sadat Mohamadnia, Abdolreza Garajei, Ata Farhadi Nasab, Abdollah Bahrami, Naghmeh |
author_sort | Bolandparva, Farzaneh |
collection | PubMed |
description | INTRODUCTION: MicroRNAs (miRs) are a group of endogenous, non-coding, 18–24 nucleotide length single-strand RNAs. These molecules mediate the gene expression and are involved in regulating diverse cellular biological processes, i.e. cell cycle, differentiation, and apoptosis. Aberrant miR expression has been shown to be an important event in the pathologies of various types of cancer, including oral squamous cell carcinoma (OSCC). METHODS: Blood samples were obtained from 30 patients (15 cases and 15 controls), to determine miR-138 and miR-424-5p expression by using real-time PCR and ΔΔCT. RESULTS: The median CT values of miR-138 were 27.60 and 28.70, while those of miR 424-5p were 29.40 and 30.0 in the case and control groups, respectively. Mann-Whitney test indicated no significant difference in miR-138 and miR-424-5p between the two groups (P > 0.05). However, results obtained by ΔΔCT method showed that miR-424-5p expression was 1.96 times higher in the case group, but miR-138 expression was 3.05 times lower in the plasma of OSCC patients. CONCLUSION: Our findings suggest that the evaluation of miR-138 and miR-424-5p expression in serum can be used as potent markers for carcinoma detection and also may be a potentially therapeutic approach in the future. Further longitudinal studies with larger samples are required to verify these findings. |
format | Online Article Text |
id | pubmed-8607090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-86070902021-11-26 Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker Bolandparva, Farzaneh Hashemi Nasab, Mahboobeh Sadat Mohamadnia, Abdolreza Garajei, Ata Farhadi Nasab, Abdollah Bahrami, Naghmeh Asian Pac J Cancer Prev Research Article INTRODUCTION: MicroRNAs (miRs) are a group of endogenous, non-coding, 18–24 nucleotide length single-strand RNAs. These molecules mediate the gene expression and are involved in regulating diverse cellular biological processes, i.e. cell cycle, differentiation, and apoptosis. Aberrant miR expression has been shown to be an important event in the pathologies of various types of cancer, including oral squamous cell carcinoma (OSCC). METHODS: Blood samples were obtained from 30 patients (15 cases and 15 controls), to determine miR-138 and miR-424-5p expression by using real-time PCR and ΔΔCT. RESULTS: The median CT values of miR-138 were 27.60 and 28.70, while those of miR 424-5p were 29.40 and 30.0 in the case and control groups, respectively. Mann-Whitney test indicated no significant difference in miR-138 and miR-424-5p between the two groups (P > 0.05). However, results obtained by ΔΔCT method showed that miR-424-5p expression was 1.96 times higher in the case group, but miR-138 expression was 3.05 times lower in the plasma of OSCC patients. CONCLUSION: Our findings suggest that the evaluation of miR-138 and miR-424-5p expression in serum can be used as potent markers for carcinoma detection and also may be a potentially therapeutic approach in the future. Further longitudinal studies with larger samples are required to verify these findings. West Asia Organization for Cancer Prevention 2021-07 /pmc/articles/PMC8607090/ /pubmed/34319042 http://dx.doi.org/10.31557/APJCP.2021.22.7.2185 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bolandparva, Farzaneh Hashemi Nasab, Mahboobeh Sadat Mohamadnia, Abdolreza Garajei, Ata Farhadi Nasab, Abdollah Bahrami, Naghmeh Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title | Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title_full | Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title_fullStr | Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title_full_unstemmed | Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title_short | Early Diagnosis of Oral Squamous Cell Carcinoma (OSCC) by miR-138 and miR-424-5p Expression as a Cancer Marker |
title_sort | early diagnosis of oral squamous cell carcinoma (oscc) by mir-138 and mir-424-5p expression as a cancer marker |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607090/ https://www.ncbi.nlm.nih.gov/pubmed/34319042 http://dx.doi.org/10.31557/APJCP.2021.22.7.2185 |
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