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Clinical application of plasma mitochondrial DNA content in patients with lung cancer

机译:血浆线粒体DNA含量在肺癌患者中的临床应用

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摘要

Alterations of mitochondrial DNA (mtDNA) have been identified in several types of solid tumor. However, to the best of our knowledge, the clinical significance of plasma mtDNA content in lung cancer remains unknown. Thus, the current study explored the diagnostic and prognostic value of plasma mtDNA quantification in patients with lung cancer. Plasma mtDNA copy numbers of patients with lung cancer (n=128) and healthy individuals (n=107) were quantified by quantitative polymerase chain reaction. Plasma mtDNA copy numbers in patients and healthy controls were 0.89×104 and 1.37×104 copies/µl, respectively (P<0.0001). Furthermore, lower plasma mtDNA content was associated with tumor size, lymph node metastases, distant metastases and serum carcinoembryonic antigen levels (P<0.05), but was not associated with pathological type, age, sex or main driver gene mutation status (P>0.05). Plasma mtDNA facilitated the detection of lung cancer at a threshold of 1.19×104 copies/µl with a sensitivity of 71.1% and specificity of 70.1%, as determined by receiver operating characteristic curve analysis. Advanced stage (III and IV) patients with a lower mtDNA copy number (cutoff: 1.02×104 copies/µl) tended to exhibit poorer prognosis (P<0.05). These results indicated that plasma mtDNA content is a promising and complementary candidate with tissue mtDNA for diagnosis and prognostic prediction for lung cancer.
机译:线粒体DNA(mtDNA)的改变已在几种类型的实体瘤中得到鉴定。然而,据我们所知,肺癌中血浆mtDNA含量的临床意义仍然未知。因此,本研究探讨了血浆mtDNA定量对肺癌患者的诊断和预后价值。通过定量聚合酶链反应对肺癌患者(n = 128)和健康个体(n = 107)的血浆mtDNA拷贝数进行定量。患者和健康对照组的血浆mtDNA拷贝数分别为0.89×10 4 和1.37×10 4 拷贝/μl(P <0.0001)。此外,血浆mtDNA含量降低与肿瘤大小,淋巴结转移,远处转移和血清癌胚抗原水平相关(P <0.05),但与病理类型,年龄,性别或主要驱动基因突变状态无关(P> 0.05)。 )。血浆mtDNA通过接受者操作特征曲线分析确定,以1.19×10 4 拷贝/微升的阈值促进了肺癌的检测,灵敏度为71.1%,特异性为70.1%。 mtDNA拷贝数较低(临界值:1.02×10 4 拷贝/μl)的晚期(III和IV)患者预后较差(P <0.05)。这些结果表明血浆mtDNA含量是与组织mtDNA一起用于肺癌诊断和预后预测的有前途的补充候选物。

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