Evidence map›Paper›PMID 35264437›Full record

ArticleJournal for immunotherapy of cancer2022

Necroptosis-driving genes

Lorenzo Nicolè, Tiziana Sanavia, Rocco Cappellesso, Valeria Maffeis, Jun Akiba, Akihiko Kawahara, Yoshiki Naito, Claudia Maria Radu, Paolo Simioni, Davide Serafin and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 59 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

15 authors at 5 institutions in 2 countries.

Lorenzo Nicolè *Department of Medicine (DIMED), University of Padova, Padova, Italy.ORCID 0000-0001-8126-9674
Tiziana Sanavia *Department of Medical Sciences, University of Torino, Torino, Italy.ORCID 0000-0003-3288-0631
Rocco CappellessoDepartment of Pathology, Padova University Hospital, Padova, Italy.
Valeria MaffeisDepartment of Pathology, Azienda ULSS2 Marca Trevigiana, Treviso, Italy.
Jun AkibaDepartment of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.
Akihiko KawaharaDepartment of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.
Yoshiki NaitoDepartment of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.
Claudia Maria RaduDepartment of Medicine, General Internal Medicine and Thrombotic and Hemorrhagic Diseases Unit, University of Padova, Padova, Italy.
Paolo SimioniDepartment of Medicine, General Internal Medicine and Thrombotic and Hemorrhagic Diseases Unit, University of Padova, Padova, Italy.
Davide SerafinDepartment of Statistical Sciences, University of Padova, Padova, Italy.
Giuliana CorteseDepartment of Statistical Sciences, University of Padova, Padova, Italy.
Maria GuidoDepartment of Medicine (DIMED), University of Padova, Padova, Italy.
Giacomo ZanusDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Hirohisa YanoDepartment of Pathology, Kurume University School of Medicine, Kurume, Japan.
Ambrogio FassinaDepartment of Medicine (DIMED), University of Padova, Padova, Italy ambrogio.fassina@unipd.it.
University of Padua · ITKurume University Hospital · JPAULSS 2 Marca Trevigiana · ITKurume University · JPUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a highly lethal cancer and the second leading cause of cancer-related deaths worldwide. As demonstrated in other solid neoplasms and HCC, infiltrating CD8

methodsWe investigated the association between the main necroptosis-related genes, that is,

resultsOur findings highlighted the immunogenetic role of necroptosis and its potential prognostic role in HCC: RIPK1, RIPK3 and MLKL-p were found significantly associated with intratumoral CD3

conclusionsOur results confirmed the immunogenetic properties of necroptosis (NCP) in human HCC, showing that tumor-infiltrating lymphocytes (TILs) and, specifically, CD8+ T cells accumulate in tumors with higher expression of the necroptosis-related genes. These results suggest the importance of further studies to better assess the specific composition, as well as the functional features of the immune environment associated with a necroptotic signature in order to explore new possible diagnostic and immunotherapeutic scenarios.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsCD8-Positive T-LymphocytesCell CountHumansNecroptosisPrognosisProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesMLKL protein, humanProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, humanRIPK3 protein, humanadaptive immunityliver neoplasmslymphocytestumor-infiltrating

Identifiers

PMID35264437
PMCPMC8915343
OpenAlexW4220967518

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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.