Evidence map›Paper›PMID 33804482›Full record

ArticleCancers2021

Quantitative Assessment of CD200 and CD200R Expression in Lung Cancer.

Ioannis A Vathiotis, Tyler MacNeil, Jon Zugazagoitia, Konstantinos N Syrigos, Thazin Nwe Aung, Aaron M Gruver, Peter Vaillancourt, Ina Hughes, Steve Hinton, Kyla Driscoll and 1 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Emerging Immune Checkpoint Molecules on Cancer Cells: CD24 and CD200.International journal of molecular sciences · 2023
    Review
  6. An Immune-Related Gene Signature for Predicting Survival and Immunotherapy Efficacy in Esophageal Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2023
    Article
  7. Article
  8. Development of an immunohistochemical assay for Siglec-15.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  9. Article
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

11 authors at 3 institutions in 2 countries.

Ioannis A VathiotisDepartment of Pathology, BML 116, Yale University School of Medicine, 310 Cedar St. P.O. Box 208023, New Haven, CT 06520-8023, USA.ORCID 0000-0002-1772-5986
Tyler MacNeilDepartment of Pathology, BML 116, Yale University School of Medicine, 310 Cedar St. P.O. Box 208023, New Haven, CT 06520-8023, USA.
Jon ZugazagoitiaDepartment of Pathology, BML 116, Yale University School of Medicine, 310 Cedar St. P.O. Box 208023, New Haven, CT 06520-8023, USA.
Konstantinos N SyrigosDepartment of Medicine, National and Kapodistrian University of Athens School of Medicine, 11527 Athens, Greece.
Thazin Nwe AungDepartment of Pathology, BML 116, Yale University School of Medicine, 310 Cedar St. P.O. Box 208023, New Haven, CT 06520-8023, USA.
Aaron M GruverEli Lilly and Company, Indianapolis, IN 46285, USA.
Peter VaillancourtEli Lilly and Company, Indianapolis, IN 46285, USA.
Ina HughesEli Lilly and Company, Indianapolis, IN 46285, USA.
Steve HintonEli Lilly and Company, Indianapolis, IN 46285, USA.
Kyla DriscollEli Lilly and Company, Indianapolis, IN 46285, USA.
David L RimmDepartment of Pathology, BML 116, Yale University School of Medicine, 310 Cedar St. P.O. Box 208023, New Haven, CT 06520-8023, USA.ORCID 0000-0001-5820-4397
Eli Lilly (United States) · USYale University · USNational and Kapodistrian University of Athens · GR

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Kurt A Schalper · 2015 to 2026
$31.1M
Eli Lilly and Company CO01.GR102387.CC1037.PG00032.PJ000001.DLR2.FD28NCATS NIH HHS UL1 TR001863NCI NIH HHS P50 CA196530Yale SPORE in Lung Cancer CO01.GR107062.CC1037.PG00032.PJ000001.DLR2.FD02
6 · The paper itself

Abstract

CD200/CD200R is an immune checkpoint with broad expression patterns and a potential target for immune therapy. In this study, we assess both CD200 and CD200R expression in solid tumors, with a focus on lung cancer, and evaluate their association with clinicopathologic characteristics, mutation status, outcome, and programmed death-ligand 1 (PD-L1) expression. We used multiplexed quantitative immunofluorescence (QIF) to measure the expression of CD200 and CD200R in a total of 455 patients from three lung cancer cohorts. Using carefully validated antibodies, we performed target measurement with tyramide-based QIF panels and analyzed the data using the PM2000 microscope and AQUA software. CD200 tumor positivity was found in 29.7% of non-small cell lung cancer (NSCLC) patients and 33.3% of lung large cell neuroendocrine carcinoma (LCNEC) patients. CD200 demonstrated notable intratumoral heterogeneity. CD200R was expressed in immune cells in 25% of NSCLC and 41.3% of LCNEC patients. While CD200R is predominantly expressed in immune cells, rare tumor cell staining was seen in a highly heterogeneous pattern. CD200R expression in the stromal compartment was significantly higher in patients with squamous differentiation (

Indexed as

CD200CD200Rimmunotherapylung cancerNSCLC

Identifiers

PMID33804482
PMCPMC7957629
OpenAlexW3134842203

What OpenQuestion holds

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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.