The association of transcription factor Prox1 with the proliferation, migration, and invasion of lung cancer

被引:3
|
作者
Hao, Xinxin [1 ,2 ,3 ]
Luo, Wenting [4 ]
Qiu, Xueshan [1 ,2 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Pathol, Shenyang 110001, Peoples R China
[2] China Med Univ, Coll Basic Med Sci, Shenyang 110001, Peoples R China
[3] China Med Univ, Dept Blood Transfus, Shengjing Hosp, Shenyang 110004, Peoples R China
[4] China Med Univ, Key Lab, Hlth Minist Congenital Malformat, Shengjing Hosp, Shenyang 110004, Peoples R China
来源
OPEN LIFE SCIENCES | 2021年 / 16卷 / 01期
关键词
lung cancer; transcription factor Prox1; Rho family; migration; invasion; EXPRESSION; CELLS; CHINA; BETA;
D O I
10.1515/biol-2021-0056
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background - The current study investigates the effect of transcription factor Prox1 on the proliferation, migration, and invasion ability of lung cancer. Methods - Lung cancer cell lines (A549 and H446 cells) were transfected with Prox1NAD and siRNA, respectively. Thus, the A549 and H446 cells overexpressed Prox1 after transfection of Prox1NAD plasmids, and A549 and H446 cells have low expression of Prox1 after transfection with siRNA. Reverse transcriptase quantitative PCR and western blot analyses were used to detect Prox1 mRNA and protein expression in cells. Plate clone formation experiments and MTT experiments were used to detect cell proliferation. Western blot was used to detect the expression of Rho family-related proteins in cells. Results - Compared to untransfected wild-type A549 and H446 that served as blank controls, the expression level of ProxlmRNA and protein in A549 and H446 cells overexpressing Prox1 after plasmid transfection was high, while the expression level of ProxlmRNA and protein in A549 and H446 cells with low expression of Prox1 after siRNA transfection was low. With the increase of Prox1 expression, the expression of RhoA and RhoC increased, while the expression of RhoB decreased. Conclusion - The finding of this study may provide a new approach for the treatment of lung cancer using targeted gene therapy.
引用
收藏
页码:602 / 610
页数:9
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