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pmid:40044876

The LncRNA lnc-POTEM-4:14 promotes HCC progression by interacting with FOXK1.

Bo Peng · Zhipeng Quan · Lixing Liang · Mingjiang Liu · Kai Hu · Shilian Chen · Qiuli Xie · Jing Qin · Jingzhao Chen · Lijuan Liao · Songqing He · Zeyuan Li

Scientific reports · 2025 doi:10.1038/s41598-025-92614-4

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
The LncRNA lnc-POTEM-4:14 promotes HCC progression by interacting with FOXK1.
doi
10.1038/s41598-025-92614-4
pmid
40044876
authors array · 12 items
[0]
Bo Peng
[1]
Zhipeng Quan
[2]
Lixing Liang
[3]
Mingjiang Liu
[4]
Kai Hu
[5]
Shilian Chen
[6]
Qiuli Xie
[7]
Jing Qin
[8]
Jingzhao Chen
[9]
Lijuan Liao
[10]
Songqing He
[11]
Zeyuan Li
journal
Scientific reports
year
2025
abstract
Hepatocellular carcinoma (HCC) is one of the most common malignant tumours of the digestive tract and poses a serious threat to human life. This study first analysed two GEO datasets (GSE166705 and GSE115018) to screen for differentially expressed lncRNAs between HCC and adjacent tissues. The lncRNA lnc-POTEM-4:14 was determined via a series of methods to be closely related to liver cancer. Further research was subsequently performed to investigate the role of the lncRNA lnc-POTEM-4:14 in the progression of HCC. The lncRNA lnc-POTEM-4:14 is localized primarily within the nucleus and is highly expressed in liver cancer tissues. We established lnc-POTEM-4:14 knockdown and overexpression cell lines to analyse the role of lnc-POTEM-4:14 in liver cancer through functional experiments such as qPCR and WB. We identified FOXK1 as an RNA-binding protein (RBP) of lnc-POTEM-4:14 that participates in MAPK signal activation and cell cycle progression by regulating the activation or expression levels of the downstream target protein TAB1 as a transcription factor. The restoration of FOXK1 can rescue the limited proliferation and increased apoptosis caused by lnc-POTEM-4:14 knockdown. Finally, we validated our hypothesis in a nude mouse tumour-bearing model. In conclusion, lnc-POTEM-4:14 affects the progression of HCC through the FOXK1/TAB1/NLK axis, suggesting that lnc-POTEM-4:14 has potential as a therapeutic target for treating this aggressive malignancy.
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lnc-POTEM-4:14 affects the progression of HCC through the FOXK1/TAB1/NLK axis, suggesting that lnc-POTEM-4:14 has potential as a therapeutic target for treating this aggressive malignancy.
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In conclusion, lnc-POTEM-4:14 affects the progression of HCC through the FOXK1/TAB1/NLK axis, suggesting that lnc-POTEM-4:14 has potential as a therapeutic target for treating this aggressive malignancy.
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lnc-POTEM-4:14 affects the progression of HCC through the FOXK1/TAB1/NLK axis, suggesting that lnc-POTEM-4:14 has potential as a therapeutic target for treating this aggressive malignancy.
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Simultaneous control of non-coding RNA on the G2/M phase of the cell cycle in hepatocellular carcinoma [lncRNA and mRNA]
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