Inhibitory effects of circR-127aa on gastric cancer progression and tumor growth.
This study investigates the function of a newly identified 127-amino acid peptide, circR-127aa, encoded by hsa_circ_0075402 (circRACK1), in gastric cancer (GC), a condition with significant prevalence
APA
Qiao L, Pan W, et al. (2025). Inhibitory effects of circR-127aa on gastric cancer progression and tumor growth.. Cellular signalling, 125, 111520. https://doi.org/10.1016/j.cellsig.2024.111520
MLA
Qiao L, et al.. "Inhibitory effects of circR-127aa on gastric cancer progression and tumor growth.." Cellular signalling, vol. 125, 2025, pp. 111520.
PMID
39581359
Abstract
This study investigates the function of a newly identified 127-amino acid peptide, circR-127aa, encoded by hsa_circ_0075402 (circRACK1), in gastric cancer (GC), a condition with significant prevalence in China. Utilizing a comprehensive analysis of circular RNA (circRNA) ribosome profiling data alongside experimental validations through mass spectrometry, Western blot, and immunofluorescence, we demonstrate that circR-127aa Inhibits Malignant Phenotypes and suppresses tumor growth in nude mice models. Significantly, the interaction of circR-127aa with Vimentin, a crucial element in actin-actin-cytoskeletal remodeling, indicates that circR-127aa functions as a tumor suppressor by facilitating the ubiquitination of Vimentin. These findings advance our comprehension of gastric cancer (GC) progression and propose circR-127aa as a promising therapeutic target and biomarker in the management of GC.
MeSH Terms
Stomach Neoplasms; Gene Expression Regulation, Neoplastic; Cell Line, Tumor; Humans; RNA, Circular; Vimentin; Peptides; Tumor Suppressor Proteins; Ubiquitination; Biomarkers, Tumor; Animals; Mice; Actin Cytoskeleton; Gene Knockdown Techniques; Mice, Nude; Xenograft Model Antitumor Assays; Tumor Burden; Molecular Targeted Therapy; Cell Proliferation
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