Evidence map›Paper›PMID 28679835›Full record

ReviewMolecular cancer therapeutics2017

New B7 Family Checkpoints in Human Cancers.

Ling Ni, Chen Dong

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cancer therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed, 2 pooled it
7.8field-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

146 citing papers in PubMed, 2 syntheses or guidelines pooled it, 252 citations in OpenAlex.

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86 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

2 authors at 1 institution in 1 country.

Ling NiInstitute for Immunology and School of Medicine, Tsinghua University, Beijing, China. lingni@tsinghua.edu.cn.
Chen DongInstitute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
Tsinghua University · CN

Funding

Immune Tolerance Mediated by Negative Costimulatory MoleculesR01AI054912 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DONG, CHEN · 2007 to 2011
$1.9M
NIAID NIH HHS R01 AI054912
6 · The paper itself

Abstract

T cells are the main effector cells in immune response against tumors. The activation of T cells is regulated by the innate immune system through positive and negative costimulatory molecules. Targeting immune checkpoint regulators such as programmed cell death 1 (PD-1)/PD-1 ligand 1 (PD-L1) and CTL antigen 4 (CTLA-4) has achieved notable benefit in a variety of cancers, which leads to multiple clinical trials with antibodies targeting the other related B7/CD28 family members. Recently, five new B7 family ligands, B7-H3, B7-H4, B7-H5, B7-H6, and B7-H7, were identified. Here we review recent understanding of new B7 family checkpoint molecules as they have come to the front of cancer research with the concept that tumor cells exploit them to escape immune surveillance. The aim of this article is to address the structure and expression of the new B7 family molecules as well as their roles in controlling and suppressing immune responses of T cells as well as NK cells. We also discuss clinical significance and contribution of these checkpoint expressions in human cancers.

Indexed as

B7 AntigensB7-H1 AntigenCell Line, TumorCTLA-4 AntigenGene Expression Regulation, NeoplasticHumansKiller Cells, NaturalProgrammed Cell Death 1 ReceptorT-LymphocytesB7 AntigensB7-H1 AntigenCD274 protein, humanCTLA-4 AntigenPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID28679835
PMCPMC5568666
OpenAlexW2728083530

What OpenQuestion holds

Textmetadata
LicenceTDM
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.