Evidence map›Paper›PMID 35053610›Full record

ArticleCancers2022

Novel Risk Classification Based on Pyroptosis-Related Genes Defines Immune Microenvironment and Pharmaceutical Landscape for Hepatocellular Carcinoma.

Jianye Wang, Ying Wang, Marcella Steffani, Christian Stöß, Donna Ankerst, Helmut Friess, Norbert Hüser, Daniel Hartmann

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 10 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

8 authors at 2 institutions in 1 country.

Jianye WangDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0001-6291-376X
Ying WangChair of Livestock Biotechnology, School of Life Sciences Weihenstephan, Technical University of Munich, Liesel Beckman Str. 1, 85354 Freising, Germany.ORCID 0000-0003-2736-6419
Marcella SteffaniDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0002-7439-7851
Christian StößDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0002-0682-8808
Donna AnkerstDepartments of Mathematics and Life Science Systems, Technical University of Munich, Boltzmannstr. 3, 85748 Garching, Germany.
Helmut FriessDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.
Norbert HüserDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.
Daniel HartmannDepartment of Surgery, TUM School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0003-4366-8986
TUM Klinikum · DETechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence has indicated that pyroptosis functions in the development of cancer. Nonetheless, specific roles of pyroptosis-related genes in tumor progression, immune response, prognosis, and immunotherapy have not been thoroughly elucidated. After a comprehensive evaluation of pyroptosis genes, unsupervised clustering was performed to generate three distinct clusters from hepatocellular carcinoma (HCC) samples. Three distinct pyroptosis-related molecular subtypes comprising three gene clusters that had differential prognostic effects on patient survival were then identified. Immune characteristics analyses revealed diversified immune cell infiltration among the subtypes. Two clusters served as immune-hot phenotypes associated with significantly poorer survival compared to a remaining third immune-cold cluster. Among these, the immune-hot clusters were characterized by abundant adaptive immune cell infiltration, active CD4+ and CD8+ T cells, high total leukocyte counts and tumor growth status, and lower Th17 cell and M2 macrophage densities. Then, risk scores indicated that low-risk patients were more sensitive to anti-tumor therapy. Subsequently, we found a significant correlation between pyroptosis and prognosis in HCC and that pyroptosis genes drive the heterogeneity of the tumor microenvironment. The risk scoring system, based on pyroptosis-related differentially expressed genes, was established to evaluate the individual outcomes and contribute to new insights into the molecular characterization of pyroptosis-related subtypes.

Indexed as

HCCimmunotherapyprognosispyroptosistumor microenvironment

Identifiers

PMID35053610
PMCPMC8773536
OpenAlexW4206734647

What OpenQuestion holds

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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.