Autophagy-associated circRNA circATG7 facilitates autophagy and promotes pancreatic cancer progression

• Published in: Cell death & disease Vol. 13; no. 3; p. 233
• Main Authors: He, Zhiwei, Cai, Kun, Zeng, Zhirui, Lei, Shan, Cao, Wenpeng, Li, Xiaowu
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 14.03.2022; Springer Nature B.V; Nature Publishing Group
• Subjects: 13/1; 13/105; 13/109; 13/44; 13/51; 14/105; 14/19; 14/28; 14/32; 38/77; 631/67/1504/1713; 692/699/67/1504/1713; 82/16; 82/29; 82/51; 82/79; 82/80; 82/81; Antibodies; Autophagy; Autophagy - genetics; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Culture; Cell growth; Cell proliferation; Cell Proliferation - genetics; Chromosome 5; Cytoplasm; Gene Expression Regulation, Neoplastic - genetics; Humans; HuR protein; Hypoxia; Immunology; Kinases; Life Sciences; Lymph nodes; Metastases; MicroRNAs - genetics; MicroRNAs - metabolism; mRNA stability; Pancreatic cancer; Pancreatic Neoplasms; Pancreatic Neoplasms - genetics; Pheochromocytoma cells; RNA, Circular - genetics; Therapeutic targets; Tumors
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-022-04677-0

Dysregulation of autophagy and circular RNAs (circRNAs) are involved in the pancreatic cancer (PC) progression. However, the regulatory network between circRNAs, autophagy, and PC progression remains unknown. Herein, we demonstrated that autophagy-associated circRNA circ-autophagy related 7 (circATG7) was elevated in PC tissues compared to adjacent tissues, and in PC cells treated with EBSS and hypoxia. circATG7 expression was positively associated with tumor diameter and lymph node invasion in patients with PC. circATG7 overexpression promoted PC cell proliferation, mobility, and autophagy in vitro, while circATG7 knockdown induced the opposite effects. ATG7 inhibition attenuated the effects of circATG7 on the biological functions of PC cells. CircATG7 is located in the cell cytoplasm and nucleus. Cytoplasmic circATG7 sponged miR-766-5p and decreased its expression, and increased the expression of ATG7, a target gene of miR-766-5p. Nuclear circATG7 acted as a scaffold to increase the interaction between the human antigen R protein and ATG7 mRNA and enhanced ATG mRNA stability. Furthermore, we demonstrated that circATG7 regulates PC cell proliferation and metastasis in vivo via ATG7-dependent autophagy. In conclusion, our results demonstrated that circATG7 accelerates PC progression via miR-766-5p/ATG7 and that HUR/ATG7 depends on autophagic flux. Thus, circATG7 may be a potential therapeutic target for PC.