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DOI 10.1038/s41598-025-92614-4

Медицинская библиотека · Scientific reports · 2025

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

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

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Аннотация

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.

Для цитирования: Peng Bo, Quan Zhipeng, Liang Lixing, Liu Mingjiang, Hu Kai, Chen Shilian, Xie Qiuli, Qin Jing, Chen Jingzhao, Liao Lijuan, He Songqing, Li Zeyuan. The LncRNA lnc-POTEM-4:14 promotes HCC progression by interacting with FOXK1.. Scientific reports. 2025. DOI: 10.1038/s41598-025-92614-4.

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