Evidence map›Paper›PMID 35031777›Full record

ReviewNature reviews. Cancer2022

Programmed death ligand 1 signals in cancer cells.

Anand V R Kornepati, Ratna K Vadlamudi, Tyler J Curiel

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 212 papers.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed
40.7field-weighted citation impact, top 1% 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

212 citing papers in PubMed, 392 citations in OpenAlex.

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  18. Immunobiological mechanisms of action of oncolytic peptides.Journal for immunotherapy of cancer · 2026
    Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Anand V R KornepatiGraduate School of Biomedical Sciences, University of Texas Health San Antonio, San Antonio, TX, USA.
Ratna K VadlamudiGraduate School of Biomedical Sciences, University of Texas Health San Antonio, San Antonio, TX, USA.
Tyler J CurielGraduate School of Biomedical Sciences, University of Texas Health San Antonio, San Antonio, TX, USA. curielt@uthscsa.edu.ORCID 0000-0001-6962-9411
The University of Texas MD Anderson Cancer Center · USThe University of Texas Health Science Center at San Antonio · US

Funding

Role of cell-intrinsic effects of PD-L1 in carcinogenesisF30CA239390 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KORNEPATI, ANAND · 2020 to 2023
$130k
NCI NIH HHS F30 CA239390
6 · The paper itself

Abstract

The paradigm of surface-expressed programmed death ligand 1 (PDL1) signalling to immune cell programmed death 1 (PD1) to inhibit antitumour immunity has helped to develop effective and revolutionary immunotherapies using antibodies blocking these cell-extrinsic interactions. The recent discovery of cancer cell-intrinsic PDL1 signals has broadened understanding of pathologic tumour PDL1 signal consequences that now includes control of tumour growth and survival pathways, stemness, immune effects, DNA damage responses and gene expression regulation. Many such effects are PD1-independent. These insights demonstrate that the prevailing cell-extrinsic PDL1 signalling paradigm is useful, but incomplete in important respects. This Perspective discusses historical and recent advances in understanding cancer cell-intrinsic PDL1 signals, mechanisms for signal controls and important immunopathologic consequences including resistance to cytotoxic agents, targeted small molecules and immunotherapies. Cancer cell-intrinsic PDL1 signals present novel drug discovery targets and also have potential as reliable treatment response biomarkers. Cancer cell-intrinsic PD1 signals and cell-intrinsic PDL1 signals in non-cancer cells are discussed briefly, as are PDL1 signals from soluble and vesicle-bound PDL1 and PDL1 isoforms. We conclude with suggestions for addressing the most pressing challenges and opportunities in this rapidly developing field.

Indexed as

B7-H1 AntigenNeoplasmsDrug DiscoveryHumansImmunotherapyB7-H1 Antigen

Identifiers

PMID35031777
PMCPMC9989967
OpenAlexW4206324389

What Socratic 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 Socratic graph.