Evidence map›Paper›PMID 26235173›Full record

ArticleInternational journal of cancer2016

Mesenchymal stem cells regulate melanoma cancer cells extravasation to bone and liver at their perivascular niche.

Diego Correa, Rodrigo A Somoza, Paul Lin, William P Schiemann, Arnold I Caplan

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.6field-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

43 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  4. Molecular Underpinnings of Brain Metastases.International journal of molecular sciences · 2025
    Review
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  20. The Habitat Assay, a Platform to StudyTissue engineering. Part A · 2020
    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

5 authors at 1 institution in 1 country.

Diego CorreaDepartment of Biology, Skeletal Research Center, Case Western Reserve University, Cleveland, OH.
Rodrigo A SomozaDepartment of Biology, Skeletal Research Center, Case Western Reserve University, Cleveland, OH.
Paul LinDepartment of Biology, Skeletal Research Center, Case Western Reserve University, Cleveland, OH.
William P SchiemannCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH.
Arnold I CaplanDepartment of Biology, Skeletal Research Center, Case Western Reserve University, Cleveland, OH.
Case Western Reserve University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Bone Marrow MSCs/Pericytes: Gatekeepers Controlling Skeletal Metastasis.R01CA163562 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI CAPLAN, ARNOLD IRWIN · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA163562NIGMS NIH HHS NIH T32 GM007250NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

Skeleton and liver are preferred organs for cancer dissemination in metastatic melanoma negatively impacting quality of life, therapeutic success and overall survival rates. At the target organ, the local microenvironment and cell-to-cell interactions between invading and resident stromal cells constitute critical components during the establishment and progression of metastasis. Mesenchymal stem cells (MSCs) possess, in addition to their cell progenitor function, a secretory capacity based on cooperativity with other cell types in injury sites including primary tumors (PT). However, their role at the target organ microenvironment during cancer dissemination is not known. We report that local MSCs, acting as pericytes, regulate the extravasation of melanoma cancer cells (MCC) specifically to murine bone marrow (BM) and liver. Intra-arterially injected wild-type MCC fail to invade those selective organs in a genetic model of perturbed pericyte coverage of the vasculature (PDGF-B(ret/ret)), similar to CD146-deficient MCC injected into wild type mice. Invading MCC interact with resident MSCs/pericytes at the perivascular space through co-expressed CD146 and Sdf-1/CXCL12-CXCR4 signaling. Implanted engineered bone structures with MSCs/pericytes deficient of either Sdf-1/CXCL12 or CD146 become resistant to invasion by circulating MCC. Collectively, the presence of MSCs/pericytes surrounding the target organ vasculature is required for efficient melanoma metastasis to BM and liver.

Indexed as

AnimalsBone NeoplasmsDisease Models, AnimalGene Knockdown TechniquesHumansLiver NeoplasmsMelanomaMesenchymal Stem CellsMiceMice, TransgenicNeoplasm InvasivenessPericytesTumor MicroenvironmentCD146mesenchymal stem cells (MSCs)metastatic melanomapericytesSdf-1

Identifiers

PMID26235173
PMCPMC4882929
OpenAlexW1501668303

What OpenQuestion holds

Textmetadata
LicenceTDM
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.