Abstract
Background/Aims
Aberrant Peroxisomal Biogenesis Factor 26 (PEX26) occurs in multiple cell process. However, the role of PEX26 in colorectal cancer (CRC) development remains unknown. We aimed to study PEX26 expression, regulation, and function in CRC cells.
Methods
Using the bioinformatic analysis, real-time quantitative PCR, and immunohistochemistry staining, we detected the expression of PEX26 in CRC and normal tissues. We performed functional experiments in vitro to elucidate the effect of PEX26 on CRC cells. We analyzed the RNA-seq data to reveal the downstream regulating network of PEX26.
Results
PEX26 is significantly down-regulated in CRC and its low expression correlates with the poor overall survival of CRC patients. We further demonstrated that PEX26 over-expression inhibits the ability of CRC cell migration, invasion, and epithelial–mesenchymal transition (EMT), while PEX26 knockdown promotes the malignant phenotypes of migration, invasion, and EMT via activating the Wnt pathway.
Conclusion
Overall, our results showed that the loss of PEX26 contributes to the malignant phenotype of CRC. PEX26 may serve as a novel metastasis repressor for CRC.
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Funding
This study was supported by grants from the National Natural Scientific Foundation of China (No. 81974378 and No. 82003115) and Shaanxi Fundamental Science Research Project for Chemistry & Biology (22JHQ084).
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EC and JY designed and drafted the manuscript. BY, LG, SW, MW, YT, and DY performed the experiments. LC helped analyzed the statistics. All authors read and approved the final manuscript.
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The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of Northwest University.
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Yan, B., Cao, L., Gao, L. et al. PEX26 Functions as a Metastasis Suppressor in Colorectal Cancer. Dig Dis Sci 69, 112–122 (2024). https://doi.org/10.1007/s10620-023-08168-w
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DOI: https://doi.org/10.1007/s10620-023-08168-w