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Updated: Jul 20, 2026

On-Chip Endothelial Inflammatory Phenotyping
Published on: July 21, 2012
Endothelial monocyte-activating polypeptide-II and its functions in (patho)physiological processes
Remco van Horssen1, Alexander M M Eggermont, Timo L M ten Hagen
1Laboratory of Experimental Surgical Oncology, Department of Surgical Oncology, Erasmus University MC - Daniel den Hoed Cancer Center, Rotterdam, The Netherlands. r.vanhorssen@ncmls.ru.nl
Endothelial monocyte-activating polypeptide-II (EMAP-II) is a cytokine involved in inflammation and angiogenesis. This review covers EMAP-II
Area of Science:
- Molecular Biology
- Immunology
- Cell Biology
Background:
- Endothelial monocyte-activating polypeptide-II (EMAP-II) is a pro-inflammatory cytokine.
- Its precursor, proEMAP/p43, is linked to protein translation via the tRNA multisynthetase complex.
- Both proEMAP/p43 and EMAP-II exhibit cytokine properties and affect various cell types.
Purpose of the Study:
- To review existing data on the isolation, expression, and functions of EMAP-II.
- To explore EMAP-II's roles in physiological and pathological conditions, particularly cancer.
- To discuss proEMAP/p43 processing into EMAP-II and potential therapeutic applications.
Main Methods:
- Literature review of published data.
- Analysis of studies on EMAP-II isolation and expression.
- Examination of research on EMAP-II functions in various cell types and disease models.
Main Results:
- EMAP-II possesses pro-inflammatory and anti-angiogenic activities.
- ProEMAP/p43, the precursor, also has cytokine properties and is involved in translation.
- EMAP-II and its precursor impact endothelial cells, immune cells, and fibroblasts.
Conclusions:
- EMAP-II is a multifunctional cytokine with significant roles in both normal physiology and disease, especially cancer.
- Understanding the processing of proEMAP/p43 to EMAP-II is crucial.
- EMAP-II holds potential for novel cancer therapies.
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