Runt-related transcription factor 1 promotes apoptosis and inhibits neuroblastoma progression in vitro and in vivo

Journal of Experimental & Clinical Cancer Research

Duo Li¹  Yuanyuan Chu¹  Harish C. Joshi²  Shiwang Li³  Jiarui Pu³  Qiangsong Tong³  Mei Hong³  Shaotao Tang³  Jing He⁴ 

[1] Central Laboratory, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology;Department of Cell Biology, Emory University;Department of Pediatric Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology;Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology;

关键词: Transcription factor;    Transcription regulation;    Neuroblastoma-prognosis;    Tumor progression;   

DOI  :  10.1186/s13046-020-01558-2

来源: DOAJ

【 摘 要 】

Abstract Background Runt-related transcription factor 1 (RUNX1) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters and can accelerate apoptosis in various tumors. However, the regulatory mechanisms underlying RUNX1 expression in neuroblastoma (NB), a highly malignant tumor in childhood, remain largely unclear. In this study, we aimed to assess the role of RUNX1 in NB and to reveal the underlying mechanisms that may contribute to finding a potential therapeutics strategy against NB. Methods Growth, invasion, metastasis and angiogenesis were assessed using Cell Counting Kit-8 (CCK-8) immunocytochemistry, and studies involving soft agar, cell invasion, tube formation and whole animals. The levels of expression were measured using real-time quantitative PCR for RNA, Western blot and immunostaining analyses for proteins. Luciferase reporter and chromatin immunoprecipitation assays indicated that RUNX1 directly binds within the BIRC5, CSF2RB and NFKBIA promoter regions to facilitate transcription. The level of apoptosis was assessed by determining mitochondrial membrane potential and flow cytometry. Results RUNX1 was highly expressed in ganglioneuroma (GN) and well-differentiated (WD) tissues relative to the poorly differentiated (PD) and undifferentiated (UD) ones. Moreover, RUNX1 effectively reduced cell viability, invasion, metastasis, angiogenesis, and promoted apoptosis in vitro and in vivo. RUNX1 reduced BIRC5 transcription and increased CSF2RB and NFKBIA transcription by directly binding BIRC5, CSF2RB and NFKBIA promoters. In addition, cytotoxic drugs, especially cisplatin, significantly increased RUNX1 expression in NB cells and promoted apoptosis. Conclusions These data show that RUNX1 is an independent surrogate marker for the progression of NB and it can be used for monitoring NB prognosis during therapy.

【 授权许可】

Unknown