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KCNJ14 Knockdown Significantly Inhibited the Proliferation and Migration of Colorectal Cells

Overview
Publisher Biomed Central
Specialty Genetics
Date 2022 Sep 13
PMID 36100894
Authors
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Abstract

Background: This study attempted to verify the potential of KCNJ14 as a biomarker in colorectal cancer (CRC).

Methods: Data on transcriptomics and DNA methylation and the clinical information of CRC patients were downloaded from The Cancer Genome Atlas and Gene Expression Omnibus databases. Biological information analysis methods were conducted to determine the role of KCNJ14 in the prognosis, diagnosis, immune cell infiltration, and regulation mechanism of CRC patients. The effect of KCNJ14 on the proliferation and migration of HCT116 and SW480 CRC cell lines was verified by in vitro experiments (MTT, colony-forming, wound healing, and transwell assays). Western blotting was performed to detect the effect of KCNJ14 on the levels of mTOR signalling pathway-related proteins.

Results: KCNJ14 expression was remarkably increased in CRC tissues and cell lines, which reduced the overall survival time of patients. KCNJ14 mRNA was negatively regulated by its methylation site cg17660703, which can also endanger the prognosis of patients with CRC. Functional enrichment analysis suggested that KCNJ14 is involved in the mTOR, NOD-like receptor, and VEGF signalling pathways. KCNJ14 expression was positively correlated with the number of CD4 + T cells and negatively correlated with that of CD8 + T cells in the immune microenvironment. KCNJ14 knockdown significantly reduced not only the proliferation and migration of CRC cell lines but also the levels of mTOR signalling pathway-related proteins.

Conclusions: This study not only increases the molecular understanding of KCNJ14 but also provides a potentially valuable biological target for the treatment of colorectal cancer.

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Comprehensive Analysis of KCNJ14 Potassium Channel as a Biomarker for Cancer Progression and Development.

Alasiri G Int J Mol Sci. 2023; 24(3).

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References
1.
Thuringer D, Chanteloup G, Boucher J, Pernet N, Boudesco C, Jego G . Modulation of the inwardly rectifying potassium channel Kir4.1 by the pro-invasive miR-5096 in glioblastoma cells. Oncotarget. 2017; 8(23):37681-37693. PMC: 5514940. DOI: 10.18632/oncotarget.16949. View

2.
Liu Z, Shen F, Wang H, Li A, Wang J, Du L . Abnormally high expression of HOXA2 as an independent factor for poor prognosis in glioma patients. Cell Cycle. 2020; 19(13):1632-1640. PMC: 7469623. DOI: 10.1080/15384101.2020.1762038. View

3.
Pinho R, Maga E . DNA methylation as a regulator of intestinal gene expression. Br J Nutr. 2021; 126(11):1611-1625. DOI: 10.1017/S0007114521000556. View

4.
Lee I, Lee S, Kang T, Kang W, Park C . Unconventional role of the inwardly rectifying potassium channel Kir2.2 as a constitutive activator of RelA in cancer. Cancer Res. 2012; 73(3):1056-62. DOI: 10.1158/0008-5472.CAN-12-2498. View

5.
Liu S, Fan W, Gao X, Huang K, Ding C, Ma G . Estrogen receptor alpha regulates the Wnt/β-catenin signaling pathway in colon cancer by targeting the NOD-like receptors. Cell Signal. 2019; 61:86-92. DOI: 10.1016/j.cellsig.2019.05.009. View