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The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma

OBJECTIVE: The most common histopathological subtype of lung cancer is adenocarcinoma. MicroRNAs are a class of non-coding RNAs that play roles in the regulation of gene expression. MicroRNAs affecting apoptosis may have different roles in lung adenocarcinoma development, progression, and differenti...

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Autores principales: Fakılı, Füsun, Feridun Işık, Ahmet, Kahraman, Demet, Kul, Seval, Eronat, Ömer, İlhan, Sedat, Bağcı, Cansu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Thoracic Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346105/
https://www.ncbi.nlm.nih.gov/pubmed/37503613
http://dx.doi.org/10.5152/ThoracResPract.2023.22063
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author Fakılı, Füsun
Feridun Işık, Ahmet
Kahraman, Demet
Kul, Seval
Eronat, Ömer
İlhan, Sedat
Bağcı, Cansu
author_facet Fakılı, Füsun
Feridun Işık, Ahmet
Kahraman, Demet
Kul, Seval
Eronat, Ömer
İlhan, Sedat
Bağcı, Cansu
author_sort Fakılı, Füsun
collection PubMed
description OBJECTIVE: The most common histopathological subtype of lung cancer is adenocarcinoma. MicroRNAs are a class of non-coding RNAs that play roles in the regulation of gene expression. MicroRNAs affecting apoptosis may have different roles in lung adenocarcinoma development, progression, and differentiation. The objective of this study is to profile all known microRNAs linked to apoptosis in normal and lung cancer tissue using real-time polymerase chain reaction. MATERIAL AND METHODS: Tissues with adenocarcinoma and healthy tissues were taken from the same lung. The degree of differentiation of all tumors was determined. Expressions of 84 apoptosis-associated microRNAs in both tissues were analyzed by real-time polymerase chain reaction array. RESULTS: Eleven patients and 22 samples were included in the study. In the comparison of expression levels of apoptosis-associated microRNAs in normal and adenocarcinoma tissue, miR-134, miR-183-5p, miR-192-5p, miR-193b-3, miR-194-5p, miR-200c-3, miR-212-3p, miR-25-3p, miR-449a, and miR-9-5p showed significant difference in downregulation. Receiver operating characteristic curve analysis of 10 identified microRNAs was performed, and cut-off values, sensitivity, and specificity were determined. No significant difference was found between microRNA expression levels in adenocarcinoma tissues classified as moderate-well to poorly differentiated. CONCLUSION: Differently, downregulated expressed apoptosis-associated microRNAs were detected in lung adenocarcinoma tissues. MicroRNAs can be used as biomarkers in the diagnosis in lung adenocarcinoma. The expression of microRNAs linked to apoptosis should be investigated in different lung cancer histological subtypes in order to identify potential biomarkers.
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spelling pubmed-103461052023-07-15 The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma Fakılı, Füsun Feridun Işık, Ahmet Kahraman, Demet Kul, Seval Eronat, Ömer İlhan, Sedat Bağcı, Cansu Thorac Res Pract Original Article OBJECTIVE: The most common histopathological subtype of lung cancer is adenocarcinoma. MicroRNAs are a class of non-coding RNAs that play roles in the regulation of gene expression. MicroRNAs affecting apoptosis may have different roles in lung adenocarcinoma development, progression, and differentiation. The objective of this study is to profile all known microRNAs linked to apoptosis in normal and lung cancer tissue using real-time polymerase chain reaction. MATERIAL AND METHODS: Tissues with adenocarcinoma and healthy tissues were taken from the same lung. The degree of differentiation of all tumors was determined. Expressions of 84 apoptosis-associated microRNAs in both tissues were analyzed by real-time polymerase chain reaction array. RESULTS: Eleven patients and 22 samples were included in the study. In the comparison of expression levels of apoptosis-associated microRNAs in normal and adenocarcinoma tissue, miR-134, miR-183-5p, miR-192-5p, miR-193b-3, miR-194-5p, miR-200c-3, miR-212-3p, miR-25-3p, miR-449a, and miR-9-5p showed significant difference in downregulation. Receiver operating characteristic curve analysis of 10 identified microRNAs was performed, and cut-off values, sensitivity, and specificity were determined. No significant difference was found between microRNA expression levels in adenocarcinoma tissues classified as moderate-well to poorly differentiated. CONCLUSION: Differently, downregulated expressed apoptosis-associated microRNAs were detected in lung adenocarcinoma tissues. MicroRNAs can be used as biomarkers in the diagnosis in lung adenocarcinoma. The expression of microRNAs linked to apoptosis should be investigated in different lung cancer histological subtypes in order to identify potential biomarkers. Turkish Thoracic Society 2023-05-01 /pmc/articles/PMC10346105/ /pubmed/37503613 http://dx.doi.org/10.5152/ThoracResPract.2023.22063 Text en © 2023 authors https://creativecommons.org/licenses/by-nc/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Original Article
Fakılı, Füsun
Feridun Işık, Ahmet
Kahraman, Demet
Kul, Seval
Eronat, Ömer
İlhan, Sedat
Bağcı, Cansu
The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title_full The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title_fullStr The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title_full_unstemmed The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title_short The Profiling of Apoptosis-Associated MicroRNA Expressions of the Lung Adenocarcinoma
title_sort profiling of apoptosis-associated microrna expressions of the lung adenocarcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346105/
https://www.ncbi.nlm.nih.gov/pubmed/37503613
http://dx.doi.org/10.5152/ThoracResPract.2023.22063
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