Evidence map›Paper›PMID 34639059›Full record

ReviewInternational journal of molecular sciences2021

The Positive and Negative Immunoregulatory Role of B7 Family: Promising Novel Targets in Gastric Cancer Treatment.

Nadia Bolandi, Afshin Derakhshani, Nima Hemmat, Amir Baghbanzadeh, Zahra Asadzadeh, Mina Afrashteh Nour, Oronzo Brunetti, Renato Bernardini, Nicola Silvestris, Behzad Baradaran

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.7field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 90 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Nadia BolandiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.
Afshin DerakhshaniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.ORCID 0000-0002-3243-233X
Nima HemmatImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.ORCID 0000-0001-6432-9647
Amir BaghbanzadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.
Zahra AsadzadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.
Mina Afrashteh NourImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.
Oronzo BrunettiMedical Oncology Unit-IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, 70124 Bari, Italy.ORCID 0000-0002-7014-6828
Renato BernardiniDepartment of Biomedical and Biotechnological Sciences, University of Catania, Via S. Sofia 97, 95100 Catania, Italy.
Nicola SilvestrisMedical Oncology Unit-IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, 70124 Bari, Italy.ORCID 0000-0001-7814-7318
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 516615731, Iran.ORCID 0000-0002-8642-6795
Tabriz University of Medical Sciences · IRIstituto Tumori Bari · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC), with a heterogeneous nature, is the third leading cause of death worldwide. Over the past few decades, stable reductions in the incidence of GC have been observed. However, due to the poor response to common treatments and late diagnosis, this cancer is still considered one of the lethal cancers. Emerging methods such as immunotherapy with immune checkpoint inhibitors (ICIs) have transformed the landscape of treatment for GC patients. There are presently eleven known members of the B7 family as immune checkpoint molecules: B7-1 (CD80), B7-2 (CD86), B7-H1 (PD-L1, CD274), B7-DC (PDCD1LG2, PD-L2, CD273), B7-H2 (B7RP1, ICOS-L, CD275), B7-H3 (CD276), B7-H4 (B7x, B7S1, Vtcn1), B7-H5 (VISTA, Gi24, DD1α, Dies1 SISP1), B7-H6 (NCR3LG1), B7-H7 (HHLA2), and Ig-like domain-containing receptor 2 (ILDR2). Interaction of the B7 family of immune-regulatory ligands with the corresponding receptors resulted in the induction and inhibition of T cell responses by sending co-stimulatory and co-inhibitory signals, respectively. Manipulation of the signals provided by the B7 family has significant potential in the management of GC.

Indexed as

ImmunomodulationAnimalsAntineoplastic Agents, ImmunologicalB7 AntigensBiomarkers, TumorCarrier ProteinsClinical Trials as TopicGene Expression RegulationHumansMolecular Targeted TherapyMultigene FamilyProtein BindingProtein Interaction Domains and MotifsProtein IsoformsStomach NeoplasmsTreatment OutcomeAntineoplastic Agents, ImmunologicalB7 AntigensBiomarkers, TumorCarrier ProteinsProtein IsoformsB7 familygastric cancerimmune checkpointsimmunotherapy

Identifiers

PMID34639059
PMCPMC8509619
OpenAlexW3204011947

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.