Evidence map›Paper›PMID 38137547›Full record

ReviewBiomedicines2023

CD200/CD200R: Bidirectional Role in Cancer Progression and Immunotherapy.

Christopher Nip, Leyi Wang, Chengfei Liu

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 18 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

3 authors at 2 institutions in 1 country.

Christopher NipDepartment of Urologic Surgery, University of California, Davis, CA 95817, USA.
Leyi WangDepartment of Urologic Surgery, University of California, Davis, CA 95817, USA.ORCID 0009-0008-7297-0643
Chengfei LiuDepartment of Urologic Surgery, University of California, Davis, CA 95817, USA.ORCID 0000-0002-2452-8788
Integra (United States) · USUniversity of California, Davis · US

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Gina M Dayton · 2002 to 2026
$84.9M
Dissecting the Role of Proteostasis in Anti-Androgen Resistant Prostate CancerR37CA249108 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Chengfei Liu · 2021 to 2026
$2.1M
Modulating HSP70/STUB1 machinery in therapy-resistant prostate cancerR01CA251253 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LIU, CHENGFEI · 2021 to 2025
$1.8M
Targeting intracrine steroidogenesis in anti-androgen resistant prostate cancerR21CA277171 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LIU, CHENGFEI · 2023 to 2024
$403k
NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA251253NCI NIH HHS R21 CA277171NCI NIH HHS R37 CA249108NIH HHS R01CA251253NIH HHS R37CA249108
6 · The paper itself

Abstract

As an immune checkpoint molecule, CD200 serves a foundational role in regulating immune homeostasis and promoting self-tolerance. While CD200 expression occurs in various immune cell subsets and normal tissues, its aberrant expression patterns in hematologic malignancies and solid tumors have been linked to immune evasion and cancer progression under pathological conditions, particularly through interactions with its cognate receptor, CD200R. Through this CD200/CD200R signaling pathway, CD200 exerts its immunosuppressive effects by inhibiting natural killer (NK) cell activation, cytotoxic T cell functions, and M1-polarized macrophage activity, while also facilitating expansion of myeloid-derived suppressor cells (MDSCs) and Tregs. Moreover, CD200/CD200R expression has been linked to epithelial-to-mesenchymal transition and distant metastasis, further illustrating its role in cancer progression. Conversely, CD200 has also been shown to exert anti-tumor effects in certain cancer types, such as breast carcinoma and melanoma, indicating that CD200 may exert bidirectional effects on cancer progression depending on the specific tumor microenvironment (TME). Regardless, modulating the CD200/CD200R axis has garnered clinical interest as a potential immunotherapeutic strategy for cancer therapy, as demonstrated by early-phase clinical trials. However, further research is necessary to fully understand the complex interactions of CD200 in the tumor microenvironment and to optimize its therapeutic potential in cancer immunotherapy.

Indexed as

cancerCD200CD200Rcheckpointimmunosuppressive signalingtherapytumor immune microenvironment

Identifiers

PMID38137547
PMCPMC10741515
OpenAlexW4389916017

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.