Evidence map›Paper›PMID 34572789›Full record

ArticleCancers2021

PD-L1 Dependent Immunogenic Landscape in Hot Lung Adenocarcinomas Identified by Transcriptome Analysis.

Jutta Kirfel, Christiane Charlotte Kümpers, Anke Fähnrich, Carsten Heidel, Mladen Jokic, Ignacija Vlasic, Sebastian Marwitz, Torsten Goldmann, Helen Pasternack, Sabine Bohnet and 5 more

Open access · goldAbstract 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Jutta KirfelInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Christiane Charlotte KümpersInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Anke FähnrichMedical Systems Biology Group, Luebeck Institute of Experimental Dermatology, University of Luebeck, 23538 Luebeck, Germany.
Carsten HeidelInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Mladen JokicInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Ignacija VlasicInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.ORCID 0000-0003-3506-5181
Sebastian MarwitzPathology, Research Center Borstel, Leibniz Lung Center, 23845 Borstel, Germany.ORCID 0000-0003-4920-5552
Torsten GoldmannPathology, Research Center Borstel, Leibniz Lung Center, 23845 Borstel, Germany.
Helen PasternackInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.ORCID 0000-0003-2386-2300
Sabine BohnetDepartment of Pulmonology, University Hospital Schleswig-Holstein, Campus Luebeck, Ratzeburger Allee 160, 23538 Luebeck, Germany.
Danny JonigkInstitute for Pathology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-5251-2281
Mark P KühnelInstitute for Pathology, Hannover Medical School, 30625 Hannover, Germany.
Anne OffermannInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Hauke BuschMedical Systems Biology Group, Luebeck Institute of Experimental Dermatology, University of Luebeck, 23538 Luebeck, Germany.
Sven PernerInstitute of Pathology, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
University Hospital Schleswig-Holstein · DEInstitute for Integrative and Experimental Genomics · DEMedizinische Hochschule Hannover · DEResearch Center Borstel - Leibniz Lung Center · DE

Funding

Bristol-Myers Squibb Foundation CA209-8C7
6 · The paper itself

Abstract

backgroundLung cancer is the most frequent cause of cancer-related deaths worldwide. The clinical development of immune checkpoint blockade has dramatically changed the treatment paradigm for patients with lung cancer. Yet, an improved understanding of PD-1/PD-L1 checkpoint blockade-responsive biology is warranted.

methodsWe aimed to identify the landscape of immune cell infiltration in primary lung adenocarcinoma (LUAD) in the context of tumoral PD-L1 expression and the extent of immune infiltration ("hot" vs. "cold" phenotype). The study comprises LUAD cases (

resultsGene set enrichment analysis defined complement, IL-JAK-STAT signaling, KRAS signaling, inflammatory response, TNF-alpha signaling, interferon-gamma response, interferon-alpha response, and allograft rejection as significantly upregulated pathways in the PD-L1-positive hot subgroup. Additionally, we demonstrated that STAT1 is upregulated in the PD-L1-positive hot subgroup and KIT in the PD-L1-negative hot subgroup.

conclusionThe presented study illustrates novel aspects of PD-L1 regulation, with potential biological relevance, as well as relevance for immunotherapy response stratification.

Indexed as

coldhotimmune phenotypelung adenocarcinoma (LUAD)programmed cell death-ligand 1 (PD-L1)proteintranscriptome

Identifiers

PMID34572789
PMCPMC8469831
OpenAlexW3201106729

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.