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pmid:41578763

Immune Escape-Related Gene NXT1 as a Potential Prognostic and Therapeutic Target in Hepatocellular Carcinoma.

Jia Guo · Xin Tong · Songtao Liu · Feng Liu · Yachao Qu · Ren Li · Xuli Bao

The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025 doi:10.5152/tjg.2025.24193

Paper

complete

Experiment

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Data

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Analysis

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title
Immune Escape-Related Gene NXT1 as a Potential Prognostic and Therapeutic Target in Hepatocellular Carcinoma.
doi
10.5152/tjg.2025.24193
pmid
41578763
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[0]
Jia Guo
[1]
Xin Tong
[2]
Songtao Liu
[3]
Feng Liu
[4]
Yachao Qu
[5]
Ren Li
[6]
Xuli Bao
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The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
year
2025
abstract
BACKGROUND/AIMS: Hepatocellular carcinoma (HCC) constitutes approximately 85% of liver cancers. This study aimed to investigate the role of immune escape-related genes (IEGs) in HCC patients and analyze their relationship with prognosis and immunotherapy, thereby providing a reference for further clinical treatment. MATERIALS AND METHODS: Datasets were collected from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus databases. Differential expression analysis was conducted to identify differentially expressed IEGs between normal and HCC tissues. Expression, survival, mutational, and immune profiles of a hub gene nuclear transport factor 2 like export factor 1 (NXT1) were evaluated. Validation of NXT1 expression in adjacent normal and HCC tissues was carried out using RT-qPCR and western blot assays. Next, CCK-8, wound healing, and transwell assays were conducted to evaluate the biological function of NXT1 in HCC cell lines. RESULTS: Analysis of the TCGA-LIHC and GSE164359 datasets revealed that NXT1 was notably elevated in HCC tissues compared to adjacent normal tissues, a finding validated through RT-qPCR and western blot assays. Meanwhile, high levels of NXT1 were associ ated with an unfavorable prognosis of HCC patients. Mutational analysis indicated a higher incidence of TP53 mutations in the NXT1 high-expression group relative to the NXT1 low-expression group. HCC patients with high NXT1 expression demonstrated an increased proportion of M0 macrophages and regulatory T cells (Tregs) and a decreased proportion of M1 macrophages. Furthermore, deficiency of NXT1 significantly suppressed HCC cell viability, migration, and invasion. CONCLUSION: Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC. Cite this article as: Guo J, Tong X, Liu S, et al. Immune escape-related gene NXT1 as a potential prognostic and therapeutic target in hepatocellular carcinoma. Turk J Gastroenterol. 2026;37(1):98-112.
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The approach for estimating the overall survival rates over a 10-year period among various groups was facilitated by utilizing the “survival” and “survminer” packages, which are based on the Kaplan–Meier algorithm. Furthermore, the log-rank test was employed to assess the statistical significance of disparities in survival rates among the distinct groups.
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The approach for estimating the overall survival rates over a 10-year period among various groups was facilitated by utilizing the “survival” and “survminer” packages, which are based on the Kaplan–Meier algorithm. Furthermore, the log-rank test was employed to assess the statistical significance of disparities in survival rates among the distinct groups.
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The data that support the findings of this study are available in The Cancer Genome Atlas (TCGA, https://tcga-data.nci.nih.gov/tcga/) database, the International Cancer Genome Consortium (ICGC, https://dcc.icgc.org/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) database.
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The data that support the findings of this study are available in The Cancer Genome Atlas (TCGA, https://tcga-data.nci.nih.gov/tcga/) database, the International Cancer Genome Consortium (ICGC, https://dcc.icgc.org/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) database.
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Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC.
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Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC.
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normal and HCC tissues was carried out using RT-qPCR and western blot assays. Next, CCK-8, wound
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all participating patients. Cell Culture and Transfection Transformed human liver epithelial-2 (THLE-2
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41578763", "kind": "science-record", "revision": 3, "content_hash": "sha256:fa75e785a27928cec4f9e913cc93360145199b5e95c923cbcb78d9031bd404a4", "created_at": "2026-11-01T20:31:32Z", "updated_at": "2026-11-01T22:15:21Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Immune Escape-Related Gene NXT1 as a Potential Prognostic and Therapeutic Target in Hepatocellular Carcinoma.", "doi": "10.5152/tjg.2025.24193", "pmid": "41578763", "authors": ["Jia Guo", "Xin Tong", "Songtao Liu", "Feng Liu", "Yachao Qu", "Ren Li", "Xuli Bao"], "journal": "The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology", "year": 2025, "abstract": "BACKGROUND/AIMS: Hepatocellular carcinoma (HCC) constitutes approximately 85% of liver cancers. This study aimed to investigate the role of immune escape-related genes (IEGs) in HCC patients and analyze their relationship with prognosis and immunotherapy, thereby providing a reference for further clinical treatment.\nMATERIALS AND METHODS: Datasets were collected from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus databases. Differential expression analysis was conducted to identify differentially expressed IEGs between normal and HCC tissues. Expression, survival, mutational, and immune profiles of a hub gene nuclear transport factor 2 like export factor 1 (NXT1) were evaluated. Validation of NXT1 expression in adjacent normal and HCC tissues was carried out using RT-qPCR and western blot assays. Next, CCK-8, wound healing, and transwell assays were conducted to evaluate the biological function of NXT1 in HCC cell lines.\nRESULTS: Analysis of the TCGA-LIHC and GSE164359 datasets revealed that NXT1 was notably elevated in HCC tissues compared to adjacent normal tissues, a finding validated through RT-qPCR and western blot assays. Meanwhile, high levels of NXT1 were associ ated with an unfavorable prognosis of HCC patients. Mutational analysis indicated a higher incidence of TP53 mutations in the NXT1 high-expression group relative to the NXT1 low-expression group. HCC patients with high NXT1 expression demonstrated an increased proportion of M0 macrophages and regulatory T cells (Tregs) and a decreased proportion of M1 macrophages. Furthermore, deficiency of NXT1 significantly suppressed HCC cell viability, migration, and invasion.\nCONCLUSION: Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC. Cite this article as: Guo J, Tong X, Liu S, et al. Immune escape-related gene NXT1 as a potential prognostic and therapeutic target in hepatocellular carcinoma. Turk J Gastroenterol. 2026;37(1):98-112.", "claims": [{"id": "claim-method", "statement": "The approach for estimating the overall survival rates over a 10-year period among various groups was facilitated by utilizing the “survival” and “survminer” packages, which are based on the Kaplan–Meier algorithm. Furthermore, the log-rank test was employed to assess the statistical significance of disparities in survival rates among the distinct groups.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41578763", "locator": "sections[6] \"Survival Analysis\" paragraph 2", "quote": "The approach for estimating the overall survival rates over a 10-year period among various groups was facilitated by utilizing the “survival” and “survminer” packages, which are based on the Kaplan–Meier algorithm. Furthermore, the log-rank test was employed to assess the statistical significance of disparities in survival rates among the distinct groups."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data that support the findings of this study are available in The Cancer Genome Atlas (TCGA, https://tcga-data.nci.nih.gov/tcga/) database, the International Cancer Genome Consortium (ICGC, https://dcc.icgc.org/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) database.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41578763", "locator": "sections[31] \"Data Availability Statement:\" paragraph 2", "quote": "The data that support the findings of this study are available in The Cancer Genome Atlas (TCGA, https://tcga-data.nci.nih.gov/tcga/) database, the International Cancer Genome Consortium (ICGC, https://dcc.icgc.org/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) database."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:41578763", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Collectively, NXT1 may serve as a valuable prognostic marker and a potential therapeutic target for HCC.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:41578763"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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HCCLM3 cells were transfected with siRNA negative control (siRNA NC), NXT1", "RNA1, NXT1 siRNA2, and NXT1 siRNA3 using the Transfection Kit. The siRNA sequences are summarized in S", "g 5% CO2. HCCLM3 cells were transfected with siRNA negative control (siRNA NC), NXT1 siRNA1, NX"], "order_basis": "paper_text_order:3040", "id": "assay:4"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["M) medium containing 10% FBS and 1% P/S. All cell lines were maintained at 37°C in a humidified atmosphere containin", "epithelial-2 (THLE-2) cells (IMMOCELL) were cultured in a complete Bronchial epithelial growth mediu", "LM3 (Procell) and Huh-7 (Procell) cells were cultured in a Dulbecco's Modified Eagle Medium (DMEM) me", "taining 10% FBS and 1% P/S. 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