Circ_0000705 facilitates proline metabolism of esophageal squamous cell carcinoma cells by targeting miR-621/PYCR1 axis

• Published in: Discover. Oncology Vol. 13; no. 1; p. 50
• Main Authors: Qian, Cui-juan, Tong, Yi-yang, Wu, Lin-ken, Wang, Yi-chao, Teng, Xiao-sheng, Yao, Jun
• Format: Journal Article
• Language: English
• Published: New York Springer US 22.06.2022; Springer
• Subjects: Cancer Research; Circ_0000705; ESCC; Internal Medicine; Medicine; Medicine & Public Health; miR-621; Molecular Medicine; Oncology; Proline metabolism; PYCR1; Radiotherapy; Surgical Oncology; Proline metabolism; Circ_0000705; PYCR1; miR-621; ESCC
• ISSN: 2730-6011; 2730-6011
• DOI: 10.1007/s12672-022-00513-1

CircRNAs have been found to play crucial roles in the metabolism and progression of cancers, but their roles and mechanisms in esophageal squamous cell carcinoma (ESCC) have not been fully elucidated. This work is aimed to explore the role and mechanism of hsa_circ_0000705 (circ_0000705) in ESCC. Circ_0000705 expression was up-regulated in ESCC tissues and cell lines, and high circ_0000705 expression was correlated with poor survival. Circ_0000705 facilitated cell proliferation, invasion, migration and proline metabolism of ESCC cells. The inhibitory effects of circ_0000705 knockdown on cell invasion, migration and proline metabolism were partly rescued by miR-621 inhibition or PYCR1 over-expression. Furthermore, circ_0000705 expression is negatively correlated with miR-621 expression, and positively correlated with PYCR1 in ESCC tissues. Mechanistically, circ_0000705 acted as a ceRNA by sponging miR-621, thereby facilitating PYCR1 expression in ESCC cells. In conclusion, circ_0000705 promoted proline metabolism and malignant progression of ESCC by regulating the miR‑621/PYCR1 axis.