Clinical significance of serum mitochondrial DNA in lung cancer
The aim of the study was to investigate the clinical significance of serum mitochondrial DNA (mtDNA) in lung cancer. Serum mtDNA from 65 lung cancer patients, 20 patients with benign lung diseases and 55 healthy individuals was quantified using real-time fluorescent quantitative polymerase chain rea...
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Published in | Clinical biochemistry Vol. 46; no. 15; pp. 1474 - 1477 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.10.2013
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Subjects | |
Online Access | Get full text |
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Summary: | The aim of the study was to investigate the clinical significance of serum mitochondrial DNA (mtDNA) in lung cancer.
Serum mtDNA from 65 lung cancer patients, 20 patients with benign lung diseases and 55 healthy individuals was quantified using real-time fluorescent quantitative polymerase chain reaction (FQ-PCR). Data were analyzed using statistical software SPSS 13.0.
Serum mtDNA levels in lung cancer patients were significantly higher, compared to those in patients with benign lung diseases and healthy individuals (u=108, p=0.000; u=293, p=0.000), and closely associated with TNM stage (p=0.01). The use of serum mtDNA facilitated detection of lung cancer at a cutoff value of 0.74×104copies/μL with a sensitivity of 86.2% and specificity of 80.7%. However, serum mtDNA levels were not associated with patient age, gender, histological type, and lymph node metastasis (p>0.05).
Quantification of serum mtDNA using FQ-PCR potentially serves as a novel complementary tool to improve the clinical screening and detection of lung cancer.
•Serum mtDNA were higher in lung cancer group than in benign and healthy groups.•Serum mtDNA was associated with the progress of lung cancer.•Serum mtDNA could be a novel biomarker for the clinical screening of lung cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0009-9120 1873-2933 1873-2933 |
DOI: | 10.1016/j.clinbiochem.2013.04.009 |