Evidence map›Paper›PMID 36171610›Full record

ReviewWorld journal of surgical oncology2022

Neoantigens and their clinical applications in human gastrointestinal cancers.

Zahra Shokati Eshkiki, Shahram Agah, Seidamir Pasha Tabaeian, Meghdad Sedaghat, Fatemeh Dana, Atefeh Talebi, Abolfazl Akbari

Open access · goldAbstract readReview
In one paragraph

Review in World journal of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  3. Article
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  7. Human leukocyte antigen and tumor immunotherapy (Review).International journal of oncology · 2023
    Review
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

7 authors at 4 institutions in 1 country.

Zahra Shokati EshkikiAlimentary Tract Research Center, Clinical Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.ORCID http://orcid.org/0000-0002-9478-4840
Shahram AgahColorectal Research Center, Iran University of Medical Sciences, Tehran, Iran. agah.sh@iums.ac.ir.ORCID http://orcid.org/0000-0002-5269-4644
Seidamir Pasha TabaeianColorectal Research Center, Iran University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0001-5260-5667
Meghdad SedaghatDepartment of Internal Medicine, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0002-3966-0597
Fatemeh DanaDepartment of Clinical Biochemistry, School of Medicine, Babol University of Medical Sciences, Babol, Iran.ORCID http://orcid.org/0000-0002-9780-9935
Atefeh TalebiColorectal Research Center, Iran University of Medical Sciences, Tehran, Iran.ORCID http://orcid.org/0000-0002-8144-9074
Abolfazl AkbariColorectal Research Center, Iran University of Medical Sciences, Tehran, Iran. akbari.ab@iums.ac.ir.ORCID http://orcid.org/0000-0001-5902-593X
Iran University of Medical Sciences · IRAhvaz Jundishapur University of Medical Sciences · IRBabol University of Medical Sciences · IRShahid Beheshti University of Medical Sciences · IR

Funding

Iran University of Medical Sciences. 99-3-49-19830
6 · The paper itself

Abstract

backgroundTumor-specific neoantigens are ideal targets for cancer immunotherapy. As research findings have proved, neoantigen-specific T cell activity is immunotherapy's most important determinant. MAIN TEXT: There is sufficient evidence showing the role of neoantigens in clinically successful immunotherapy, providing a justification for targeting. Because of the significance of the pre-existing anti-tumor immune response for the immune checkpoint inhibitor, it is believed that personalized neoantigen-based therapy may be an imperative approach for cancer therapy. Thus, intensive attention is given to strategies targeting neoantigens for the significant impact with other immunotherapies, such as the immune checkpoint inhibitor. Today, several algorithms are designed and optimized based on Next-Generation Sequencing and public databases, including dbPepNeo, TANTIGEN 2.0, Cancer Antigenic Peptide Database, NEPdb, and CEDAR databases for predicting neoantigens in silico that stimulates the development of T cell therapies, cancer vaccine, and other ongoing immunotherapy approaches.

conclusionsIn this review, we deliberated the current developments in understanding and recognition of the immunogenicity of newly found gastrointestinal neoantigens as well as their functions in immunotherapies and cancer detection. We also described how neoantigens are being developed and how they might be used in the treatment of GI malignancies.

Indexed as

Cancer VaccinesGastrointestinal NeoplasmsNeoplasmsAntigens, NeoplasmHumansImmune Checkpoint InhibitorsImmunotherapyPeptidesAntigens, NeoplasmCancer VaccinesImmune Checkpoint InhibitorsPeptidesCAR-T cellGastrointestinal cancersImmunotherapyNeoantigenTumor

Identifiers

PMID36171610
PMCPMC9520945
OpenAlexW4297516003

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.