Evidence map›Paper›PMID 30808673›Full record

ArticleCancer research2019

Biomaterial Scaffolds Recruit an Aggressive Population of Metastatic Tumor Cells

Grace G Bushnell, Tejaswini P Hardas, Rachel M Hartfield, Yining Zhang, Robert S Oakes, Scott Ronquist, Haiming Chen, Indika Rajapakse, Max S Wicha, Jacqueline S Jeruss and 1 more

Abstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. An engineered niche delineates metastatic potential of breast cancer.Bioengineering & translational medicine · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

11 authors.

Grace G BushnellDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan.
Tejaswini P HardasDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan.
Rachel M HartfieldDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-7112-6565
Yining ZhangDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan.
Robert S OakesDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-3783-6488
Scott RonquistDepartment of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan.
Haiming ChenDepartment of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan.
Indika RajapakseDepartment of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan.
Max S WichaDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Jacqueline S JerussDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan. ldshea@umich.edu jjeruss@med.umich.edu.
Lonnie D SheaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan. ldshea@umich.edu jjeruss@med.umich.edu.

Funding

Targeting breast cancer stem cellsR35CA197585 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WICHA, MAX S. · 2016 to 2022
$6.4M
An in vivo metastasis sensorR01CA173745 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BACKMAN, VADIM, SHEA, LONNIE D · 2012 to 2016
$4.2M
Measuring Signaling Pathway Dynamics During Tissue Growth in HydrogelsR01CA214384 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2017 to 2021
$1.8M
Heterogeneity of early metastatic tumor cellsF31CA224982 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BUSHNELL, GRACE GILMORE · 2018 to 2019
$56k
NCI NIH HHS F31 CA224982NCI NIH HHS R01 CA173745NCI NIH HHS R01 CA214384NCI NIH HHS R35 CA197585
6 · The paper itself

Abstract

For most cancers, metastasis is the point at which clinical treatment shifts from curative intent to extending survival. Biomaterial implants acting as a synthetic premetastatic niche recruit metastatic cancer cells and provide a survival advantage, and their use as a diagnostic platform requires assessing their relevance to disease progression. Here, we showed that scaffold-captured tumor cells (SCAF) were 30 times more metastatic to the lung than primary tumor (PT) cells, similar to cells derived from lung micrometastases (LUNG). SCAF cells were more aggressive

Indexed as

AnimalsApoptosisBiocompatible MaterialsBreast NeoplasmsCell MovementCell ProliferationFemaleHumansLung NeoplasmsMiceMice, Inbred NODMice, SCIDNeoplastic Stem CellsTissue ScaffoldsTranscriptomeTumor Cells, CulturedBiocompatible Materials

Identifiers

PMID30808673
PMCPMC6467791

What OpenQuestion holds

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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.