Evidence map›Paper›PMID 30906645›Full record

ArticleNature biomedical engineering2018

Implantable pre-metastatic niches for the study of the microenvironmental regulation of disseminated human tumour cells.

Ryan A Carpenter, Jun-Goo Kwak, Shelly R Peyton, Jungwoo Lee

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  6. Mechanoimmunological Control of Metastatic Site Selection.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Engineered immunological niche directs therapeutic development in models of progressive multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
  11. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Ryan A CarpenterDepartment of Chemical Engineering, Institute for Applied Life Sciences, University of Massachusetts, Amherst, MA, USA.
Jun-Goo KwakDepartment of Chemical Engineering, Institute for Applied Life Sciences, University of Massachusetts, Amherst, MA, USA.ORCID http://orcid.org/0000-0001-9527-0940
Shelly R PeytonDepartment of Chemical Engineering, Institute for Applied Life Sciences, University of Massachusetts, Amherst, MA, USA.
Jungwoo LeeDepartment of Chemical Engineering, Institute for Applied Life Sciences, University of Massachusetts, Amherst, MA, USA. jungwoo@umass.edu.ORCID http://orcid.org/0000-0003-2048-2142
University of Massachusetts Amherst · US

Funding

Elucidating Essential Components of Bone Marrow MetastasisR00CA163671 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI LEE, JUNGWOO · 2014 to 2016
$740k
NCI NIH HHS R00 CA163671
6 · The paper itself

Abstract

Cancer survivors often carry disseminated tumour cells (DTCs), yet owing to DTC dormancy they do not relapse from treatment. Understanding how the local microenvironment regulates the transition of DTCs from a quiescent state to active proliferation could suggest new therapeutic strategies to prevent or delay the formation of metastases. Here, we show that implantable biomaterial microenvironments incorporating human stromal cells, immune cells and cancer cells can be used to examine the post-dissemination phase of the evolution of the tumour microenvironment. After subdermal implantation in mice, porous hydrogel scaffolds seeded with human bone marrow stromal cells form a vascularized niche and recruit human circulating tumour cells released from an orthotopic prostate tumour xenograft. Systemic injection of human peripheral blood mononuclear cells slowed the evolution of the active metastatic niches but did not change the rate of overt metastases, as the ensuing inflammation promoted the formation of DTC colonies. Implantable pre-metastatic niches might enable the study of DTC colonization and proliferation, and facilitate the development of effective anti-metastatic therapies.

Identifiers

PMID30906645
PMCPMC6424369
OpenAlexW2896811518

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.