Evidence map›Paper›PMID 35141051›Full record

ArticleOncoimmunology2022

T cell-mediated elimination of cancer cells by blocking CEACAM6-CEACAM1 interaction.

Jessica Pinkert, Hans-Henning Boehm, Mark Trautwein, Wolf-Dietrich Doecke, Florian Wessel, Yingzi Ge, Eva Maria Gutierrez, Rafael Carretero, Christoph Freiberg, Uwe Gritzan and 21 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Article
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  5. Article
  6. A unified framework for identification of cell-type-specific spatially variable genes in spatial transcriptomic studies.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. A Novel Theranostic Strategy for Malignant Pulmonary Nodules by Targeted CECAM6 withAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Identification of CD66c as a potential target in gastroesophageal junction cancer for antibody-drug conjugate development.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
    Article
  9. Article
  10. Evolution of CEACAM pathogen decoy receptors in primates.European journal of clinical investigation · 2024
    Article
  11. Structural aspects of CEACAM1 interactions.European journal of clinical investigation · 2024
    Review
  12. Article
  13. The role of CEACAMs in neutrophil function.European journal of clinical investigation · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Phenotypic screen of sixty-eight colorectal cancer cell lines identifies CEACAM6 and CEACAM5 as markers of acid resistance.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. The emerging roles of CEACAM6 in human cancer (Review).International journal of oncology · 2024
    Review
  19. Article
  20. 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

31 authors at 4 institutions in 1 country.

Jessica PinkertJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Hans-Henning BoehmJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Mark TrautweinPharmaceutical Division, Bayer AG, Wuppertal, Germany.
Wolf-Dietrich DoeckePharmaceutical Division, Bayer AG, Berlin, Germany.
Florian WesselJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Yingzi GeJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Eva Maria GutierrezJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Rafael CarreteroJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Christoph FreibergPharmaceutical Division, Bayer AG, Wuppertal, Germany.
Uwe GritzanPharmaceutical Division, Bayer AG, Cologne, Germany.
Merlin Luetke-EverslohPharmaceutical Division, Bayer AG, Berlin, Germany.
Sven GolfierPharmaceutical Division, Bayer AG, Berlin, Germany.
Oliver Von AhsenPharmaceutical Division, Bayer AG, Berlin, Germany.
Valentina VolpinDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Antonio SorrentinoDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Anchana RathinasamyDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Maria XydiaDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Robert LohmayerDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Julian SaxDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Ayse Nur-MenevseDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Abir HusseinDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Slava StamovaDivision of Interventional Immunology, RCI Regensburg Center for Interventional Immunology, Regensburg, Germany.
Georg BeckmannPharmaceutical Division, Bayer AG, Berlin, Germany.
Julian Marius GlueckPharmaceutical Division, Bayer AG, Wuppertal, Germany.
Dorian SchoenfeldPharmaceutical Division, Bayer AG, Wuppertal, Germany.
Joerg WeiskePharmaceutical Division, Bayer AG, Berlin, Germany.
Dieter ZopfPharmaceutical Division, Bayer AG, Berlin, Germany.
Rienk OffringaJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Bertolt KreftPharmaceutical Division, Bayer AG, Berlin, Germany.
Philipp BeckhoveJoint Immunotherapeutics Laboratory of the DKFZ-Bayer Innovation Alliance, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Joerg WilludaPharmaceutical Division, Bayer AG, Berlin, Germany.
Bayer (Germany) · DEUniversity Hospital Regensburg · DEGerman Cancer Research Center · DEUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), a cell surface receptor, is expressed on normal epithelial tissue and highly expressed in cancers of high unmet medical need, such as non-small cell lung, pancreatic, and colorectal cancer. CEACAM receptors undergo homo- and heterophilic interactions thereby regulating normal tissue homeostasis and angiogenesis, and in cancer, tumor invasion and metastasis. CEACAM6 expression on malignant plasma cells inhibits antitumor activity of T cells, and we hypothesize a similar function on epithelial cancer cells. The interactions between CEACAM6 and its suggested partner CEACAM1 on T cells were studied. A humanized CEACAM6-blocking antibody, BAY 1834942, was developed and characterized for its immunomodulating effects in co-culture experiments with T cells and solid cancer cells and in comparison to antibodies targeting the immune checkpoints programmed cell death protein 1 (PD-1), programmed death-ligand 1 (PD-L1), and T cell immunoglobulin mucin-3 (TIM-3). The immunosuppressive activity of CEACAM6 was mediated by binding to CEACAM1 expressed by activated tumor-specific T cells. BAY 1834942 increased cytokine secretion by T cells and T cell-mediated killing of cancer cells. The

Indexed as

Antigens, CDNeoplasmsProgrammed Cell Death 1 ReceptorB7-H1 AntigenCell Adhesion MoleculesGPI-Linked ProteinsHumansT-LymphocytesAntigens, CDB7-H1 AntigenCD66 antigensCEACAM6 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsProgrammed Cell Death 1 ReceptorCEACAM6elimination of cancer cellshumanized antibodyimmune checkpoint inhibitorimmune responseT cell

Identifiers

PMID35141051
PMCPMC8820806
OpenAlexW4200140011

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.