Hypoxia-induced circADAMTS6 in a TDP43-dependent manner accelerates glioblastoma progression via ANXA2/ NF-κB pathway.
Shulin ZhaoBoyan LiRongrong ZhaoZiwen PanShouji ZhangWei QiuQindong GuoYanhua QiZijie GaoYang FanHao XuMing LiJian ZhangHuizhi WangJianye XuShaobo WangQingtong WangJiawei QiuLin DengXing GuoPing ZhangHao XueGang LiPublished in: Oncogene (2022)
Circular RNAs (circRNAs) play important roles in the malignant progression of tumours. Herein, we identified an unreported circRNA (hsa-circ-0072688, also named circADAMTS6) that is specifically upregulated in the hypoxic microenvironment of glioblastoma and closely correlated with poor prognosis of gliblastoma patients. We found that circADAMTS6 promotes the malignant progression of glioblastoma by promoting cell proliferation and inhibiting apoptosis. Mechanistically, the hypoxic tumour microenvironment upregulates circADAMTS6 expression through transcription factor activator protein 1 (AP-1) and RNA-binding protein TAR DNA-binding protein 43 (TDP43). Moreover, circADAMTS6 accelerates glioblastoma progression by recruiting and stabilising annexin A2 (ANXA2) in a proteasomes-dependent manner. Furthermore, we found T-5224 (AP-1 inhibitor) treatment induces downregulation of circADAMTS6 and then inhibits tumour growth. In conclusion, our findings highlight the important role of the circADAMTS6/ANXA2 axis based on hypoxic microenvironment in glioblastoma progression, as well as its regulation in NF-κB pathway. Targeting circADAMTS6 is thus expected to become a novel therapeutic strategy for glioblastoma.
Keyphrases
- poor prognosis
- binding protein
- transcription factor
- signaling pathway
- cell proliferation
- long non coding rna
- end stage renal disease
- oxidative stress
- pi k akt
- nuclear factor
- newly diagnosed
- chronic kidney disease
- lps induced
- cell death
- endoplasmic reticulum stress
- cell cycle
- peritoneal dialysis
- small molecule
- inflammatory response
- toll like receptor
- combination therapy
- amino acid
- circulating tumor cells
- dna binding