Evidence map›Paper›PMID 39375839›Full record

ReviewExpert reviews in molecular medicine2024

Repulsive guidance molecules b (RGMb): molecular mechanism, function and role in diseases.

Jie Zhang, Yijing Jiang, Zijian Zhang, Shilin Li, Haowen Fan, Jinhua Gu, Renfang Mao, Xiaohong Xu

Abstract readReview
In one paragraph

Review in Expert reviews in molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
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  4. Article
  5. Article
  6. Agouti and BMP signaling drive a naturally occurring fate conversion of melanophores to leucophores in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. 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

8 authors.

Jie ZhangDepartment of Oncology, Affiliated Tumor Hospital of Nantong University, Nantong University, Nantong, Jiangsu, People's Republic of China.
Yijing JiangDepartment of Pathophysiology, School of Medicine, Nantong University, Nantong, Jiangsu, People's Republic of China.
Zijian ZhangDepartment of Pathophysiology, School of Medicine, Nantong University, Nantong, Jiangsu, People's Republic of China.
Shilin LiDepartment of Pathophysiology, School of Medicine, Nantong University, Nantong, Jiangsu, People's Republic of China.
Haowen FanDepartment of Pathophysiology, School of Medicine, Nantong University, Nantong, Jiangsu, People's Republic of China.
Jinhua GuNantong Institute of Genetics and Reproductive Medicine, Affiliated Maternity & Child Healthcare Hospital of Nantong University, Nantong, Jiangsu, China.
Renfang MaoDepartment of Pathophysiology, School of Medicine, Nantong University, Nantong, Jiangsu, People's Republic of China.ORCID 0000-0002-8465-1614
Xiaohong XuDepartment of Oncology, Affiliated Tumor Hospital of Nantong University, Nantong University, Nantong, Jiangsu, People's Republic of China.ORCID 0009-0000-9736-0712

Funding

Distinguished Professorship Program of Jiangsu ProvinceJiangsu Postgraduate Research and Practice Innovation Project KYCX22_3357Nantong Municipal Commission of Health and Family Planning QA2021033Youth Fund of Nantong health QA2021033
6 · The paper itself

Abstract

Repulsive guidance molecule b (RGMb), a glycosylphosphatidylinositol-anchored member of the RGM family, is initially identified as a co-receptor of bone morphogenetic protein (BMP) in the nervous system. The expression of RGMb is transcriptionally regulated by dorsal root ganglion 11 (DRG11), which is a transcription factor expressed in embryonic DRG and dorsal horn neurons and plays an important role in the development of sensory circuits. RGMb is involved in important physiological processes such as embryonic development, immune response, intercellular adhesion and tumorigenesis. Furthermore, RGMb is mainly involved in the regulation of RGMb-neogenin-Rho and BMP signalling pathways. The recent discovery of programmed death-ligand 2 (PD-L2)-RGMb binding reveals that the cell signalling network and functional regulation centred on RGMb are extremely complex. The latest report suggests that down-regulation of the PD-L2-RGMb pathway in the gut microbiota promotes an anti-tumour immune response, which defines a potentially effective immune strategy. However, the biological function of RGMb in a variety of human diseases has not been fully determined, and will remain an active research field. This article reviews the properties and functions of RGMb, focusing on its role under various physiological and pathological conditions.

Indexed as

Nerve Tissue ProteinsSignal TransductionAnimalsCell Adhesion Molecules, NeuronalGPI-Linked ProteinsHumansNeoplasmsCell Adhesion Molecules, NeuronalGPI-Linked ProteinsNerve Tissue ProteinsRGMB protein, humanbone morphogenetic proteincancerdiseasesprogrammed death-ligand 2repulsive guidance molecules b

Identifiers

PMID39375839
PMCPMC11488336

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Registered trials

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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.