Thyroid Cancer-Associated Mitochondrial DNA Mutation G3842A Promotes Tumorigenicity via ROS-Mediated ERK1/2 Activation

被引:12
作者
Chen, Sixi [1 ,7 ]
Bao, Xinzhu [2 ]
Chen, Hongzhi [3 ,6 ]
Jia, Manli [4 ]
Li, Wen [4 ]
Zhang, Luyi [4 ]
Fan, Runxiao [4 ]
Fang, Hezhi [4 ]
Jin, Liqin [5 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Clin Lab Ctr, Wenzhou 325027, Zhejiang, Peoples R China
[2] Peoples Hosp Deyang City, Dept Clin Lab, Deyang, Peoples R China
[3] Cent South Univ, Natl Clin Res Ctr Metab Dis, Xiangya Hosp 2, Key Lab Diabet Immunol,Minist Educ, 139 Middle Renmin Rd, Changsha 410011, Hunan, Peoples R China
[4] Wenzhou Med Univ, Coll Lab Med & Life Sci, Key Lab Lab Med, Zhejiang Prov Key Lab Med Genet,Minist Educ, Wenzhou 325035, Zhejiang, Peoples R China
[5] Hangzhou Med Coll, Zhengjiang Prov Peoples Hosp, Affiliated Peoples Hosp, Hangzhou, Zhejiang, Peoples R China
[6] Cent South Univ, Dept Metab & Endocrinol, Xiangya Hosp 2, 139 Middle Renmin Rd, Changsha 410011, Hunan, Peoples R China
[7] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
SOMATIC MUTATIONS; CELLS; INHIBITION; GENERATION; VARIANTS; DRIVERS; REPAIR; DAMAGE; RISK; RAF;
D O I
10.1155/2022/9982449
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial DNA (mtDNA) mutations have been identified in various human cancers, including thyroid cancer. However, the relationship between mtDNA and thyroid cancer remains unclear. Previous studies by others and us strongly suggested that mtDNA mutations in complex I may participate in thyroid cancer processes according to sequencing results of thyroid cancer tissue, although the associated pathogenic processes remain unknown. Here, to investigate whether mtDNA mutations contribute to thyroid cancer, we reanalyzed our sequencing results and characterized thyroid cancer-associated mutations in the mitochondrial complex. The results identified the highest mutation frequencies in nicotinamide adenine dinucleotide hydride (NADH) dehydrogenase subunit 4 gene (ND4) and cytochrome c oxidase subunit 1 gene (COI), which also harbored the highest rates of G > A substitutions, with most of the mutations resulting in changes in the polarity of amino acids. We then established cybrids containing the G3842A mutation identified in papillary thyroid carcinoma, which revealed it as a mutation in NADH dehydrogenase subunit 1 gene (ND1) and is previously reported in follicular thyroid carcinoma, thereby suggesting a possibly pathogenic role in thyroid carcinoma. Additionally, we found that the G3842A mutation accelerates tumorigenicity and decreases the abundance and activity of mitochondrial complex I, the oxygen consumption rate, and adenosine triphosphate levels. By contrast, the levels of reactive oxygen species (ROS) were increased to activate extracellular signal-regulated kinase (ERK1/2) signaling, which contributed to tumorigenicity. These findings suggest for the first time that mtDNA mutations help drive tumor development and that G3842A may represent a new risk factor for thyroid cancer. Furthermore, our findings indicate that drugs targeting ROS and ERK1/2 may serve as a viable therapeutic strategy for thyroid cancer.
引用
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页数:16
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