This article was originally published here
J Clin Lab Anal. 2021 Jul 23:e23900. doi: 10.1002/jcla.23900. Online ahead of print.
BACKGROUND: More and more evidences demonstrate that circular RNAs (circNRAs) can encode protein. As a circRNA with translation capabilities, outcomes of circβ-catenin in non-small cell lung cancer (NSCLC) still need to be explored.
METHOD: The research methods of circβ-catenin in the article include qRT-PCR, wound healing assay, CCK-8, colony formation, and Transwell assay. Western blotting and immunofluorescence were provided to detect protein expression levels and peptide encoded by circβ-catenin, respectively.
RESULTS: A prominently higher circβ-catenin expression was found in NSCLC tissues. Silencing of circβ-catenin was able to inhibit NSCLC cell migrating, invasive, and proliferative phenotypes. Overexpression of circβ-catenin could enhance the migrating, invasive, and proliferative phenotypes of NSCLC cells. Importantly, circβ-catenin was found to encode a peptide in NSCLC cells. Silencing or overexpression of circβ-catenin could reduce or increase β-catenin protein expression via suppressing the degradation of β-catenin.
CONCLUSION: Circβ-catenin could promote NSCLC cell malignant phenotypes via peptide-regulated β-catenin pathway. Our study provided a new understanding for the mechanisms of NSCLC.