Evidence map›Paper›PMID 39090420›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2025

Novel genetic variants in the NLRP3 inflammasome-related PANX1 and APP genes predict survival of patients with hepatitis B virus-related hepatocellular carcinoma.

Yingchun Liu, Yuman Fan, Rongbin Gong, Moqin Qiu, Xiaoxia Wei, Qiuling Lin, Zihan Zhou, Ji Cao, Yanji Jiang, Peiqin Chen and 6 more

Abstract read
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Yingchun Liu *Department of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Yuman Fan *Department of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Rongbin GongDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Moqin QiuDepartment of Respiratory Oncology, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Xiaoxia WeiDepartment of Clinical Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Qiuling LinDepartment of Clinical Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Zihan ZhouDepartment of Cancer Prevention and Control, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Ji CaoDepartment of Cancer Prevention and Control, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Yanji JiangDepartment of Scientific Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Peiqin ChenEditorial Department of Chinese Journal of Oncology Prevention and Treatment, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Bowen ChenDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Xiaobing YangDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
Yuying WeiDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China.
RuoXin ZhangDepartment of Epidemiology, School of Public Health, Key Laboratory of Public Health Safety, Ministry of Education, Fudan University, Shanghai, China.
Qiuping WenDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China. wenqiuping@stu.gxmu.edu.cn.
Hongping YuDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, Guangxi, China. yuhongping@stu.gxmu.edu.cn.ORCID http://orcid.org/0000-0002-6128-0398

Funding

Key Laboratory of Early Prevention and Treatment for Regional High Frequency Tumor, Ministry of Education GKE-KF202007Overseas Expertise Introduction Center for Discipline Innovation of Food Nutrition and Human Health (111 Center) D17011the Joint Project on Regional High-Incidence Diseases Research of Guangxi Natural Science Foundation 2023GXNSFBA026091the Key Research and Development Project of Guangxi AB18050020the Youth Science Foundation of Guangxi Medical University GXMUYSF202121Youth and Middle-aged Scientific and Technological Innovation Leading Talents Program of the Corps 2021KY0099
6 · The paper itself

Abstract

backgroundThe nod-like receptor protein 3 (NLRP3) is one of the most characterized inflammasomes involved in the pathogenesis of several cancers, including hepatocellular carcinoma (HCC). However, the effects of genetic variants in the NLRP3 inflammasome-related genes on survival of hepatitis B virus (HBV)-related HCC patients are unclear.

methodsWe performed multivariable Cox proportional hazards regression analysis to evaluate associations between 299 single-nucleotide polymorphisms (SNPs) in 16 NLRP3 inflammasome-related genes and overall survival (OS) of 866 patients with HBV-related HCC. We further performed expression quantitative trait loci (eQTL) analysis using the data from the GTEx project and 1000 Genomes projects, and performed differential expression analysis using the TCGA dataset to explore possible molecular mechanisms underlying the observed associations.

resultsWe found that two functional SNPs (PANX1 rs3020013 A > G and APP rs9976425 C > T) were significantly associated with HBV-related HCC OS with the adjusted hazard ratio (HR) of 0.83 [95% confidence interval (CI) = 0.73-0.95, P = 0.008], and 1.26 (95% CI = 1.02-1.55, P = 0.033), respectively. Moreover, the eQTL analysis revealed that the rs3020013 G allele was correlated with decreased mRNA expression levels of PANX1 in both normal liver tissues (P = 0.044) and whole blood (P < 0.001) in the GTEx dataset, and PANX1 mRNA expression levels were significantly higher in HCC samples and associated with a poorer survival of HCC patients. However, we did not observe such correlations for APP rs9976425.

conclusionsThese results indicated that SNPs in the NLRP3 inflammasome-related genes may serve as potential biomarkers for HBV-related HCC survival, once replicated by additional larger studies.

Indexed as

Carcinoma, HepatocellularHepatitis BInflammasomesLiver NeoplasmsNerve Tissue ProteinsNLR Family, Pyrin Domain-Containing 3 ProteinPolymorphism, Single NucleotideAdultAgedFemaleHepatitis B virusHumansMaleMiddle AgedPrognosisQuantitative Trait LociInflammasomesNerve Tissue ProteinsNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanGenetic variantsHBV-related hepatocellular carcinomaNLRP3 inflammasomeOverall survival

Identifiers

PMID39090420
PMCPMC11782428

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.