4.3 Article

Circular RNA hsa-circ-000881 suppresses the progression of lung adenocarcinoma in vitro via a miR-665/PRICKLE2 axis

期刊

ANNALS OF TRANSLATIONAL MEDICINE
卷 9, 期 6, 页码 -

出版社

AME PUBLISHING COMPANY
DOI: 10.21037/atm-21-844

关键词

Circ-000881; miR-665; lung adenocarcinoma (LUAD); PRICKLE2; tianhuiql@126; com

资金

  1. National Natural Science Foundation of China [81672292]
  2. TaiShan Scholar Program of Shandong Province [ts201712087]

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Circ-000881 is downregulated in LUAD, and its overexpression attenuates malignant behaviors of LUAD cells, while knockdown exacerbates their malignancy. Experimental results confirm that Circ-000881 has inhibitory effects on LUAD via a miR-665/PRICKLE2 axis.
Background: Circular RNA (circRNA) has become a new focus in the field of tumor biology research in recent years. Many circRNAs have been showed to play an important role in the progression of lung adenocarcinoma (LUAD). In this work, we studied the oncological role of hsa-circ-000881 in LUAD and attempted to explore the related mechanism. Methods: The relative expressions of hsa-circ-000881, miR-665, and PRICKLE2 were detected by RTqPCR or western blot. Functional assays were conducted to analyze the role of hsa-circ-000881 in the proliferation, migration, and invasion of LUAD cells. A luciferase reporter assay was performed to verify whether hsa-circ-000881, miR-665, and PRICKLE2 interact with each other. Results: Circ-000881 was remarkably downregulated in LUAD. Overexpression of circ-000881 attenuated cell growth, migration, and invasion, whereas its knockdown enhanced the malignancy of LUAD cells. The results of luciferase reporter assay and bioinformatics analysis confirmed that circ-000881 served as a sponge for miR-665, and PRICKLE2 was a direct target of miR-665.Overexpression of miR-665 or silencing of PRICKLE2 abolished circ-000881-mediated inhibition of malignant tumor behavior in LUAD cells. Conclusions: Circ-000881 has inhibitory effects on LUAD via a miR-665/PRICKLE2 axis, suggesting that circ-000881 may be an underlying therapeutic target for LUAD.

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