Evidence map›Paper›PMID 39090641›Full record

ArticleBMC cancer2024

ADH4-a potential prognostic marker for hepatocellular carcinoma with possible immune-related implications.

Ling Li, Yong-Ta Huang, Li-Ting Wang, Xiao-Ling Wang, Zhen-Yu Chen, Shao-Lan Jiang, Qiu-Ling Zeng, Hui-Pin Huang, Xiao-Long Li

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ling Li *Department of Pathology, The People's Hospital of Guangxi Zhuang Autonomous Region, Guangxi Academy of Medical Sciences, Nanning, China.
Yong-Ta Huang *Department of Pathology, The People's Hospital of Guangxi Zhuang Autonomous Region, Guangxi Academy of Medical Sciences, Nanning, China.
Li-Ting WangGuangxi Medical University, Nanning, China.
Xiao-Ling WangGuangxi Medical University, Nanning, China.
Zhen-Yu ChenGuangxi Medical University, Nanning, China.
Shao-Lan JiangGuangxi Medical University, Nanning, China.
Qiu-Ling ZengGuangxi Medical University, Nanning, China.
Hui-Pin HuangDepartment of Clinical Laboratory, The People's Hospital of Guangxi Zhuang Autonomous Region, Guangxi Academy of Medical Sciences, Nanning, China.
Xiao-Long LiDepartment of Cell Biology and Genetics, School of Pre-Clinical Medicine, Key Laboratory of Longevity and Agingrelated Diseases of Chinese Ministry of Education, Guangxi Medical University, Nanning, 530021, China. xlongli@outlook.com.

Funding

Natural Science Foundation of Guangxi Province 2017GXNSFAA198063Natural Science Foundation of Guangxi Province 2023GXNSFBA026107Science Foundation for Young Scholars, the People's Hospital of GuangXi Autonomous Region of China QN2021-43
6 · The paper itself

Abstract

objectiveThis study aims to explore ADH4 expression in hepatocellular carcinoma (HCC), its prognostic impact, and its immune correlation to provide novel insights into HCC prognostication and treatment.

methodsHCC prognostic marker genes were rigorously selected using GEO database, Lasso regression, GEPIA, Kaplan-Meier and pROC analyses. The expression of interested markers (ADH4, DNASE1L3, RDH16, LCAT, HGFAC) in HCC and adjacent tissues was assessed by Immunohistochemistry (IHC). We observed that ADH4 exhibited low expression levels in liver cancer tissues and high expression levels in normal liver tissues. However, the remaining four genes did not manifest any statistically significant differences between hepatocellular carcinoma (HCC) tissue and adjacent non-cancerous tissue. Consequently, ADH4 became the primary focus of our research. ADH4 expression was validated by signed-rank tests and unpaired Wilcoxon rank sum tests across pan-cancer and HCC datasets. Clinical significance and associations with clinicopathological variables were determined using Kaplan-Meier, logistic regression and Cox analyses on TCGA data. The ADH4-related immune responses were explored by Spearman correlation analysis using TIMER2 data. CD68, CD4, and CD19 protein levels were confirmed by IHC in HCC and non-cancerous tissues.

resultsADH4 showed significant downregulation in various cancers, particularly in HCC. Moreover, low ADH4 expression was associated with clinicopathological variables and served as an independent prognostic marker for HCC patients. Additionally, ADH4 affects a variety of biochemical functions and may influence cancer development, prognosis, and treatment by binding to immune cells. Furthermore, at the immune level, the low expression pattern of ADH4 is TME-specific, indicating that ADH4 has the potential to be used as a target for cancer immunotherapy.

conclusionThis study highlights the diagnostic, prognostic and immunomodulatory roles of ADH4 in HCC. ADH4 could serve as a valuable biomarker for HCC diagnosis and prognosis, as well as a potential target for immunotherapeutic interventions.

Indexed as

Alcohol DehydrogenaseBiomarkers, TumorCarcinoma, HepatocellularLiver NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMalePrognosisAlcohol Dehydrogenasealcohol dehydrogenase IVBiomarkers, TumorAlcohol dehydrogenase 4 (ADH4)Hepatocellular carcinomaImmune-related

Identifiers

PMID39090641
PMCPMC11293145

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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.