Down-regulation of MTHFD2 inhibits NSCLC progression by suppressing cycle-related genes

被引:30
|
作者
Yu, Chang [1 ,2 ]
Yang, Lehe [1 ]
Cai, Mengsi [1 ]
Zhou, Feng [1 ]
Xiao, Sisi [1 ]
Li, Yaozhe [1 ]
Wan, Tingting [1 ]
Cheng, Dezhi [3 ]
Wang, Liangxing [1 ]
Zhao, Chengguang [1 ,4 ]
Huang, Xiaoying [1 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Key Lab Heart & Lung, Div Pulm Med, Wenzhou 325000, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Intervent Therapy Dept, Wenzhou, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Dept Thorac Cardiovasc, Wenzhou, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Sch Pharmaceut Sci, Chem Biol Res Ctr, Bldg 11,Chashan St, Wenzhou 325035, Zhejiang, Peoples R China
关键词
bioinformatics; cell cycle; methylenetetrahydrofolate dehydrogenase 2; non-small cell lung cancer; CELL-PROLIFERATION; CANCER; METABOLISM; RESISTANCE; TARGET;
D O I
10.1111/jcmm.14844
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) is a bifunctional enzyme located in the mitochondria. It has been reported to be overexpressed in several malignancies. However, the relationship between the expression of MTHFD2 and non-small cell lung cancer (NSCLC) remains largely unknown. In this study, we found that MTHFD2 was significantly overexpressed in NSCLC tissues and cell lines. Knockdown of MTHFD2 resulted in reduced cell growth and tumorigenicity in vitro and in vivo. Besides, the mRNA and protein expression level of cell cycle genes, such as CCNA2, MCM7 and SKP2, was decreased in MTHFD2 knockdown H1299 cells. Our results indicate that the inhibitory effect of MTHFD2 knockdown on NSCLC may be mediated via suppressing cell cycle-related genes. These findings delineate the role of MTHFD2 in the development of NSCLC and may have potential applications in the treatment of NSCLC.
引用
收藏
页码:1568 / 1577
页数:10
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