Evidence map›Paper›PMID 41388158›Full record

ReviewJournal of molecular medicine (Berlin, Germany)2025

The multifaceted roles of MCAM in development, homeostasis, pathological conditions, and cancer.

Bartosz Mierzejewski, Dominika Kulma, Edyta Brzoska

Abstract readReview
In one paragraph

Review in Journal of molecular medicine (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

3 authors.

Bartosz MierzejewskiFaculty of Biology, Department of Cytology, University of Warsaw, Miecznikowa 1 St, 02-096, Warsaw, Poland. b.mierzejewski@uw.edu.pl.ORCID http://orcid.org/0000-0001-7517-349X
Dominika KulmaFaculty of Biology, Department of Cytology, University of Warsaw, Miecznikowa 1 St, 02-096, Warsaw, Poland.
Edyta BrzoskaFaculty of Biology, Department of Cytology, University of Warsaw, Miecznikowa 1 St, 02-096, Warsaw, Poland.

Funding

Narodowe Centrum Nauki 2021/41/N/NZ5/00504
6 · The paper itself

Abstract

MCAM (melanoma cell adhesion molecule), identified in human melanoma in 1987, has garnered attention due to its diverse roles in development, homeostasis, and various diseases, including cancer. Initially recognized for its differential expression in tumors, MCAM plays a crucial role in cell adhesion, migration, and signaling. It acts as a receptor for multiple ligands, impacting angiogenesis, inflammation, and immune responses. MCAM is expressed in developing embryos and is implicated in trophoblast invasion during implantation, serving as a marker for placental health. In adults, MCAM is predominantly found in the vascular system and modulates endothelium homeostasis and inflammatory processes. Moreover, its involvement in cancer is marked by associations with tumor progression, particularly through epithelial-mesenchymal transition (EMT) pathways, highlighting its potential as a prognostic biomarker. Elevated levels of soluble MCAM have been linked to poor outcomes in various malignancies and can influence tumor microenvironments. This review synthesizes current understanding of MCAM's multifunctional roles, its bidirectional influence in health and disease, and its potential as a therapeutic target in cancer.

Indexed as

CD146 AntigenHomeostasisNeoplasmsAnimalsEpithelial-Mesenchymal TransitionHumansSignal TransductionTumor MicroenvironmentCD146 AntigenAdhesion moleculesAngiogenesisCancerEmbryonic developmentInflammationMCAM

Identifiers

PMID41388158
PMCPMC12701039

What Socratic 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 Socratic graph.