Key Laboratory of Laboratory Medicine, Ministry of Education, Zhejiang Provincial Key Laboratory of Medical Genetics, College of Laboratory Medicine and Life Sciences, Wenzhou Medical University, China; Department of Clinical Laboratory, Nanjing Jiangbei People's Hospital Affiliated of Nantong University, China.
University of Texas Health San Antonio, United States.
Mitochondrion. 2020 Nov;55:145-153. doi: 10.1016/j.mito.2020.09.007. Epub 2020 Oct 7.
Thyroid cancer is the most common endocrine malignancy, and its incidence continues to rise. For clinicians with cancer patients, choosing and interpreting diagnostic laboratory studies has become increasingly important. Previously, changes in plasma free mitochondrial DNA levels have been found in colorectal, breast, lung, and urinary cancers, and have demonstrated diagnostic value. In this study, we investigated whether the occurrence and development of thyroid cancer might be predicted using mtDNA copy number (ND1), mtDNA integrity (ND4/ND1) and levels of cell-free nDNA (GAPDH). We analyzed ND1, ND4, and GAPDH levels in plasma and blood cells from 75 patients with thyroid cancer, 40 patients with nodular goiter, and 107 normal controls using real-time PCR. Although both the thyroid nodule and thyroid cancer patients had significantly increased ND1 levels, the ND4/ND1 ratio in the thyroid cancer group was higher than the thyroid nodule group (P < 0.05), and significantly higher than the normal control group (P < 0.01). Plasma levels of nuclear DNA (GAPDH) in the thyroid cancer group were also higher compared to normal (P < 0.05). These results indicate that increased intactness of plasma free mtDNA is associated with increased levels of plasma cell-free nDNA, and that the ND4/ND1 ratio has the potential to be a new detection indicator in thyroid cancer. Furthermore, we classified thyroid cancer patients according to clinical data including age, tumor size, and metastasis. We found significantly higher levels of GAPDH in malignant tissues. Because ND4/ND1 correlated with plasma GAPDH in the plasma studies, this also suggests a potential relationship between ND4 intactness and thyroid tumor tissue size. Taken together, our findings suggest a tumor-specific process involving increased release of intact mtDNA, detectable in the plasma, which differentiates normal patients from patients with thyroid cancer.
甲状腺癌是最常见的内分泌恶性肿瘤,其发病率持续上升。对于有癌症患者的临床医生来说,选择和解释诊断性实验室研究变得越来越重要。先前已经发现,在结直肠癌、乳腺癌、肺癌和膀胱癌中,血浆游离线粒体 DNA 水平的变化与癌症的发生和发展有关,并具有诊断价值。在这项研究中,我们研究了使用 mtDNA 拷贝数(ND1)、mtDNA 完整性(ND4/ND1)和细胞游离 nDNA(GAPDH)水平是否可以预测甲状腺癌的发生和发展。我们使用实时 PCR 分析了 75 例甲状腺癌患者、40 例甲状腺结节患者和 107 例正常对照者的血浆和血细胞中的 ND1、ND4 和 GAPDH 水平。虽然甲状腺结节和甲状腺癌患者的 ND1 水平均显著升高,但甲状腺癌组的 ND4/ND1 比值高于甲状腺结节组(P<0.05),且显著高于正常对照组(P<0.01)。甲状腺癌组的血浆核 DNA(GAPDH)水平也高于正常对照组(P<0.05)。这些结果表明,血浆游离 mtDNA 完整性的增加与血浆细胞游离 nDNA 水平的增加有关,ND4/ND1 比值有可能成为甲状腺癌的新检测指标。此外,我们根据年龄、肿瘤大小和转移等临床数据对甲状腺癌患者进行分类。我们发现恶性组织中的 GAPDH 水平显著升高。由于 ND4/ND1 在血浆研究中与血浆 GAPDH 相关,这也表明 ND4 完整性与甲状腺肿瘤组织大小之间可能存在潜在关系。总之,我们的研究结果表明,肿瘤特异性过程涉及完整 mtDNA 的释放增加,可在血浆中检测到,可将正常患者与甲状腺癌患者区分开来。