Evidence map›Paper›PMID 37248957›Full record

ArticleJournal of cellular and molecular medicine2023

An inflammation-associated ferroptosis signature optimizes the diagnosis, prognosis evaluation and immunotherapy options in hepatocellular carcinoma.

Wan-Yuan Ruan, Lu Zhang, Shan Lei, Zhi-Rui Zeng, Yu-Shi Yang, Wen-Peng Cao, Qiu-Yao Hao, Min Lu, Xiao-Bin Tian, Pai-Lan Peng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Wan-Yuan RuanDepartment of Gastroenterology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Lu ZhangSchool of Clinical Medicine, Guizhou Medical University, Guiyang, China.
Shan LeiSchool of Basic Medicine, Guizhou Medical University, Guiyang, China.
Zhi-Rui ZengSchool of Basic Medicine, Guizhou Medical University, Guiyang, China.ORCID 0000-0001-9547-9074
Yu-Shi YangDepartment of Pathology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Wen-Peng CaoSchool of Basic Medicine, Guizhou Medical University, Guiyang, China.
Qiu-Yao HaoSchool of Clinical Medicine, Guizhou Medical University, Guiyang, China.
Min LuDepartment of Gastroenterology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Xiao-Bin TianSchool of Clinical Medicine, Guizhou Medical University, Guiyang, China.
Pai-Lan PengDepartment of Gastroenterology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Guiyang Medical University · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation and ferroptosis crosstalk complexly with immune microenvironment of hepatocellular carcinoma (HCC), thus affecting the efficacy of immunotherapy. Herein, our aim was to identify the inflammation-associated ferroptosis (IAF) biomarkers for contributing HCC. A total of 224 intersecting DEGs identified from different inflammation- and ferroptosis-subtypes were set as IAF genes. Seven of them including ADH4, APOA5, CFHR3, CXCL8, FTCD, G6PD and PON1 were used for construction of a risk model which classified HCC patients into two groups (high and low risk). HCC patients in the high-risk group exhibited shorter survival rate and higher immune score, and were predicted to have higher respond rate in immune checkpoint inhibition (ICI) therapy. Levels of the seven genes were significantly changed in HCC tissues in comparison to adjacent tissues. After inserting the gene expression into the risk model, we found that the risk model exhibited the higher diagnostic value for distinguish HCC tissues compared each single gene. Furthermore, HCC tissues from our research group with high-risk score exhibited more cases of microsatellite instability (MSI), heavier tumour mutational burden (TMB), higher expression level of PDL1 and cells with CD8. Knockdown of APOA5 reduced HCC cell proliferation combining with elevating inflammation and ferroptosis levels. In conclusion, we considered APOA5 maybe a novel target for suppressing HCC via simultaneously elevating inflammation and ferroptosis levels, and signature constructed by seven IAF genes including ADH4, APOA5, CFHR3, CXCL8, FTCD, G6PD and PON1 can act as a biomarker for optimising the diagnosis, prognosis evaluation and immunotherapy options in HCC patients.

Indexed as

Carcinoma, HepatocellularFerroptosisLiver NeoplasmsAryldialkylphosphataseHumansImmunotherapyInflammationTumor MicroenvironmentAryldialkylphosphatasePON1 protein, humandiagnosishepatocellular carcinomaimmunotherapy optimisationinflammation-associated ferroptosis geneprognosis evaluation

Identifiers

PMID37248957
PMCPMC10315780
OpenAlexW4378745786

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LicenceCC BY
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Registered trials

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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.