Evidence map›Paper›PMID 35008303›Full record

ArticleCancers2021

Novel Molecular Targets for Hepatocellular Carcinoma.

Beatrice Cavalluzzo, Angela Mauriello, Concetta Ragone, Carmen Manolio, Maria Lina Tornesello, Franco M Buonaguro, Siri Amanda Tvingsholm, Sine Reker Hadrup, Maria Tagliamonte, Luigi Buonaguro

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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

16 citing papers in PubMed.

  1. Article
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  10. Cross-reactive CD8Journal of experimental & clinical cancer research : CR · 2024
    Article
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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.

Beatrice CavalluzzoInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.ORCID 0000-0002-3254-0322
Angela MaurielloInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.
Concetta RagoneInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.
Carmen ManolioInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.
Maria Lina TorneselloMolecular Biology and Viral Oncogenesis Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.ORCID 0000-0002-3523-3264
Franco M BuonaguroMolecular Biology and Viral Oncogenesis Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.
Siri Amanda TvingsholmT-Cells and Cancer, Experimental & Translational Immunology (XTI), Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Sine Reker HadrupT-Cells and Cancer, Experimental & Translational Immunology (XTI), Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Maria TagliamonteInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.
Luigi BuonaguroInnovative Immunological Models Unit, Istituto Nazionale Tumori-IRCCS-"Fond G. Pascale", 80131 Naples, Italy.

Funding

CAMPANIA REGION 4/2019CAMPANIA REGION 423/2018European Commission 602893European Commission 643638
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the third leading cause of death from cancer globally. Indeed, only a few treatments are available, most of which are effective only for the early stages of the disease. Therefore, there is an urgent needing for potential markers for a specifically targeted therapy. Candidate proteins were selected from datasets of The Human Protein Atlas, in order to identify specific tumor-associated proteins overexpressed in HCC samples associated with poor prognosis. Potential epitopes were predicted from such proteins, and homology with peptides derived from viral proteins was assessed. A multiparametric validation was performed, including recognition by PBMCs from HCC-patients and healthy donors, showing a T-cell cross-reactivity with paired epitopes. These results provide novel HCC-specific tumor-associated antigens (TAAs) for immunotherapeutic anti-HCC strategies potentially able to expand pre-existing virus-specific CD8

Indexed as

cancer immunotherapyhepatocellular carcinomatumor-associated antigens

Identifiers

PMID35008303
PMCPMC8750630

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.