Evidence map›Paper›PMID 38424542›Full record

ArticleMolecular cancer2024

Targeted deletion of CD244 on monocytes promotes differentiation into anti-tumorigenic macrophages and potentiates PD-L1 blockade in melanoma.

Jeongsoo Kim, Tae-Jin Kim, Sehyun Chae, Hyojeong Ha, Yejin Park, Sunghee Park, Chul Joo Yoon, Seon Ah Lim, Hyemin Lee, Jiyoung Kim and 14 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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  18. SLAM family-mediated crosstalk between tumor and immune cells in the tumor microenvironment: a promising biomarker and a potential therapeutic target for immune checkpoint therapies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  19. Article
  20. Heterogeneity of monocytes in cancer.American journal of cancer research · 2025
    Review
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

24 authors at 5 institutions in 2 countries.

Jeongsoo Kim *Department of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Tae-Jin Kim *Department of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Sehyun Chae *Division of Chemical Engineering and Bioengineering, College of Art, Culture and Engineering, Kangwon National University, Chuncheon, 24341, South Korea.
Hyojeong HaDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Yejin ParkDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Sunghee ParkDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Chul Joo YoonDepartment of Chemical and Biological Engineering, College of Engineering, Korea University, Seoul, 02841, South Korea.
Seon Ah LimDepartment of Life Science, Ewha Womans University, Seoul, 03760, South Korea.
Hyemin LeeDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Jiyoung KimDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Jungwon KimDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Kyungtaek ImDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Kyunghye LeeDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Jeongmin KimDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Daham KimDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Eunju LeeDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Min Hwa ShinDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Serk In ParkDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea.
Inmoo RheeDepartment of Integrative Bioscience and Biotechnology, Sejong University, Seoul, 05006, South Korea.
Keehoon JungDepartment of Biomedical Sciences, Department of Anatomy and Cell Biology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Jeewon LeeDepartment of Chemical and Biological Engineering, College of Engineering, Korea University, Seoul, 02841, South Korea.
Keun Hwa LeeDepartment of Microbiology, College of Medicine, Hanyang University, Seoul, 04763, South Korea. yomust7@gmail.com.
Daehee HwangSchool of Biological Sciences, Seoul National University, Seoul, 08826, South Korea. daehee@snu.ac.kr.
Kyung-Mi LeeDepartment of Biochemistry and Molecular biology, College of Medicine, Korea University, Seoul, 02841, South Korea. kyunglee@korea.ac.kr.
Korea University · KRSeoul National University · KREwha Womans University · KRKangwon National University · KRSejong University · KR

Funding

Korea Health Industry Development Institute HD22C2045National Research Foundation of Korea RS-2023-00225581
6 · The paper itself

Abstract

backgroundIn the myeloid compartment of the tumor microenvironment, CD244 signaling has been implicated in immunosuppressive phenotype of monocytes. However, the precise molecular mechanism and contribution of CD244 to tumor immunity in monocytes/macrophages remains elusive due to the co-existing lymphoid cells expressing CD244.

methodsTo directly assess the role of CD244 in tumor-associated macrophages, monocyte-lineage-specific CD244-deficient mice were generated using cre-lox recombination and challenged with B16F10 melanoma. The phenotype and function of tumor-infiltrating macrophages along with antigen-specific CD8 T cells were analyzed by flow cytometry and single cell RNA sequencing data analysis, and the molecular mechanism underlying anti-tumorigenic macrophage differentiation, antigen presentation, phagocytosis was investigated ex vivo. Finally, the clinical feasibility of CD244-negative monocytes as a therapeutic modality in melanoma was confirmed by adoptive transfer experiments.

resultsCD244

conclusionOur study highlights the novel role of CD244 on monocytes/macrophages in restraining anti-tumorigenic macrophage generation and tumor antigen-specific T cell response in melanoma. Importantly, our findings suggest that CD244-deficient macrophages could potentially be used as a therapeutic agent in combination with immune checkpoint inhibitors. Furthermore, CD244 expression in monocyte-lineage cells serve as a prognostic marker in cancer patients.

Indexed as

MelanomaMonocytesAnimalsB7-H1 AntigenCarcinogenesisCD8-Positive T-LymphocytesHumansMacrophagesMiceSignaling Lymphocytic Activation Molecule FamilyTumor MicroenvironmentB7-H1 AntigenCD244 protein, humanSignaling Lymphocytic Activation Molecule FamilyCD244DifferentiationImmune checkpoint blockadeMacrophage-based cell therapyMacrophagesMelanoma

Identifiers

PMID38424542
PMCPMC10903025
OpenAlexW4392298240

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.