Tuberc Respir Dis > Volume 71(1); 2011 > Article
Tuberculosis and Respiratory Diseases 2011;71(1):8-14.
DOI: https://doi.org/10.4046/trd.2011.71.1.8    Published online July 1, 2011.
MicroRNA-23a: A Novel Serum Based Diagnostic Biomarker for Lung Adenocarcinoma.
Yu Mi Lee, Hyun Jung Cho, Soo Young Lee, Seong Cheol Yun, Ji Hye Kim, Shin Yup Lee, Sun Jung Kwon, Eugene Choi, Moon Jun Na, Jae Ku Kang, Ji Woong Son
1Department of Internal Medicine, Konyang University Hospital, Konyang University College of Medicine, Daejeon, Korea. sk1609@hanmail.net
2Department of Laboratory Medicine, Konyang University Hospital, Konyang University College of Medicine, Daejeon, Korea.
3Myunggok Research Institute for Medical Science, Konyang University Hospital, Konyang University College of Medicine, Daejeon, Korea.
4Department of Internal Medicine, Kyungpook National University Hospital, Kyungpook National University College of Medicine, Daegu, Korea.
5Department of Pharmacology, Konyang University College of Medicine, Daejeon, Korea.
Abstract
BACKGROUND
MicroRNAs (miRNAs) have demonstrated their potential as biomarkers for lung cancer diagnosis. In recent years, miRNAs have been found in body fluids such as serum, plasma, urine and saliva. Circulating miRNAs are highly stable and resistant to RNase activity along with, extreme pH and temperatures in serum and plasma. In this study, we investigated serum miRNA profiles that can be used as a diagnostic biomarker of non-small cell lung cancer (NSCLC). METHODS: We compared the expression profile of miRNAs in the plasma of patients diagnosed with lung cancer using an miRNA microarray. The data from this assay were validated by quantitative real-time PCR (qRT-PCR). RESULTS: Six miRNAs were overexpressed and three miRNAs were underexpressed in both tissue and serum from squamous cell carcinoma (SCC) patients. Sixteen miRNAs were overexpressed and twenty two miRNAs were underexpressed in both tissue and serum from adenocarcinoma (AC) patients. Of the four miRNAs chosen for qRT-PCR analysis, the expression of miR-23a was consistent with microarray results from AC patients. Receiver operating characteristic (ROC) curve analyses were done and revealed that the level of serum miR-23a was a potential marker for discriminating AC patients from chronic obstructive pulmonary disease (COPD) patients. CONCLUSION: Although a small number of patients were examined, the results from our study suggest that serum miR-23a can be used in the diagnosis of AC.
Key Words: MicroRNAs, Gene Expression Profiling, Biological Markers, Lung Neoplasms


ABOUT
ARTICLE & TOPICS
Article category

Browse all articles >

Topics

Browse all articles >

BROWSE ARTICLES
FOR CONTRIBUTORS
Editorial Office
101-605, 58, Banpo-daero, Seocho-gu (Seocho-dong, Seocho Art-Xi), Seoul 06652, Korea
Tel: +82-2-575-3825, +82-2-576-5347    Fax: +82-2-572-6683    E-mail: katrdsubmit@lungkorea.org                

Copyright © 2024 by The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved.

Developed in M2PI

Close layer
prev next