Inhibitory role of ATF3 in gastric cancer progression through regulating cell EMT and stemness

Cancer Cell International

Yirong Tang¹  Xiukang Wang¹  Renli Chen¹  Xiaolan Lai¹  Fangjing Zheng²  Chuanqian Huang²  Zichun Chen³ 

[1] Department of Hematology and Rheumatism, Ningde Municipal Hospital Affiliated to Ningde Normal University;Department of Medical Oncology and Radiotherapy, Ningde Municipal Hospital Affiliated to Ningde Normal University;Department of Pharmacy, Ningde Municipal Hospital Affiliated to Ningde Normal University;

关键词: ATF3;    Migration;    Invasion;    Stemness;    Epithelial mesenchymal transition;    Gastric cancer cell line;   

DOI  :  10.1186/s12935-021-01828-9

来源: DOAJ

【 摘 要 】

Abstract Background Gastric cancer (GC) is one of the most common cancers and the third leading cause of cancer related mortality worldwide. The 5-year survival rate is rather low owing to advanced unresectable and distant metastasis. The EMT has been widely implicated in the stemness, metastatic dormancy, and chemoresistance of different solid tumors. Given the fact that activating transcription factor-3 (ATF3) is a member of the ATF/CREB family of transcription factors and its role in regulation of GC recurrence and metastasis remain poorly understood, the aim of the present study was to investigate its potential impact in epithelial–mesenchymal transition (EMT) and cancer stem cell (CSC) properties and GC aggression. Methods To elucidate the potential role of ATF3 in gastric cancer, we utilized SGC-7901 and MGC-803 gastric cancer cell lines as research models and constructed stable cell lines overexpressing ATF3. We conducted a series of assays including cell proliferation, colony formation, cell migration, tumorsphere formation, and invasion to investigate the functional roles of ATF3 in stemness of gastric cancer. The possible effect of ATF3 on epithelial–mesenchymal transition (EMT) was assessed through flow cytometry and qRT-PCR. In vivo functional effect of upregulation of ATF3 on tumor growth was examined in a mouse xenograft model. Results We found that overexpression of ATF3 inhibited cell proliferation, colony formation, cell migration and invasion. In addition, up-regulation of ATF3 attenuated tumorsphere formation, cell stemness, and potentially decreased expression of EMT markers. Moreover, ATF3 overexpression inhibited tumorigenesis in mouse xenograft model. Conclusion Our data suggest a suppressive role of ATF3 in gastric cancer development. Our findings will provide a potential therapeutic strategy and novel drug target for gastric cancer.

【 授权许可】

Unknown