scholarly journals DPPIV promotes endometrial carcinoma cell proliferation, invasion and tumorigenesis

Oncotarget ◽  
2017 ◽  
Vol 8 (5) ◽  
pp. 8679-8692 ◽  
Author(s):  
Xiaoqing Yang ◽  
Xinhua Zhang ◽  
Rongrong Wu ◽  
Qicheng Huang ◽  
Yao Jiang ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Endometrial Carcinoma ◽  
Carcinoma Cell ◽  
Endometrial Carcinoma Cell

scholarly journals lncRNA-ZFAS1 promotes the progression of endometrial carcinoma by targeting miR-34b to regulate VEGFA expression

Open Medicine ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. 1472-1481
Author(s):  
Hongli Zhu ◽  
Qihui Cheng ◽  
Hong Cai
Keyword(s):  
Cell Proliferation ◽  
Endometrial Carcinoma ◽  
Noncoding Rna ◽  
Carcinoma Cell ◽  
Underlying Mechanism ◽  
Carcinoma Cells ◽  
Factor X ◽  
Endometrial Carcinoma Cell ◽  
Proliferation And Metastasis ◽  
Cell Proliferation And Metastasis

Abstract Zinc finger nuclear transcription factor, X-box binding 1-type containing 1 antisense RNA 1 (ZFAS1) functions as an oncogenic long noncoding RNA (lncRNA) to promote proliferation and metastasis of endometrial carcinoma cell; however, the underlying mechanism has not been fully understood. First, RT-qPCR analysis of endometrial carcinoma tissues and cells showed that ZFAS1 was enriched in endometrial carcinoma tissues and cells. miR-34b was reduced in endometrial carcinoma and suggested negative correlation with ZFAS1 in endometrial carcinoma. Second, functional assays demonstrated that siRNA-mediated silence of ZFAS1 suppressed endometrial carcinoma cell proliferation and metastasis. Third, ZFAS1 bind to miR-34b and negatively regulate expression of miR-34b in endometrial carcinoma cells. miR-34b also bind to and negatively regulate expression of vascular endothelial growth factor A (VEGFA) in endometrial carcinoma cells. Lastly, knockdown of miR-34b counteracted with the suppressive effects of ZFAS1 silence on endometrial carcinoma cell proliferation and metastasis. In conclusion, lncRNA ZFAS1 functioned as an oncogene to promote endometrial carcinoma cell proliferation and metastasis through miR-34b/VEGFA axis.

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