Evidence map›Paper›PMID 28649015›Full record

ArticleBiomaterials2017

On-command on/off switching of progenitor cell and cancer cell polarized motility and aligned morphology via a cytocompatible shape memory polymer scaffold.

Jing Wang, Andy Quach, Megan E Brasch, Christopher E Turner, James H Henderson

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Cell-Responsive Shape Memory Polymers.ACS biomaterials science & engineering · 2022
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Modeling neoplastic disease with spheroids and organoids.Journal of hematology & oncology · 2020
    Review
  13. Article
  14. Cellular and Subcellular Contact Guidance on Microfabricated Substrates.Frontiers in bioengineering and biotechnology · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. 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 2 institutions in 1 country.

Jing WangDepartment of Biomedical and Chemical Engineering, Syracuse University, NY, 13244, USA; Syracuse Biomaterials Institute, Syracuse University, NY, 13244, USA.
Andy QuachDepartment of Biomedical and Chemical Engineering, Syracuse University, NY, 13244, USA; Syracuse Biomaterials Institute, Syracuse University, NY, 13244, USA.
Megan E BraschDepartment of Biomedical and Chemical Engineering, Syracuse University, NY, 13244, USA; Syracuse Biomaterials Institute, Syracuse University, NY, 13244, USA.
Christopher E TurnerDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, NY 13210, USA.
James H HendersonDepartment of Biomedical and Chemical Engineering, Syracuse University, NY, 13244, USA; Syracuse Biomaterials Institute, Syracuse University, NY, 13244, USA. Electronic address: jhhender@syr.edu.
Syracuse University · USSUNY Upstate Medical University · US

Funding

STRUCTURE AND FUNCTION OF PAXILLINR01GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1996 to 2017
$5.5M
Paxillin and Hic-5 in Coordination of Cancer Cell Invasion MechanismsR01CA163296 · NCI · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA163296NIGMS NIH HHS R01 GM047607
6 · The paper itself

Abstract

In vitro biomaterial models have enabled advances in understanding the role of extracellular matrix (ECM) architecture in the control of cell motility and polarity. Most models are, however, static and cannot mimic dynamic aspects of in vivo ECM remodeling and function. To address this limitation, we present an electrospun shape memory polymer scaffold that can change fiber alignment on command under cytocompatible conditions. Cellular response was studied using the human fibrosarcoma cell line HT-1080 and the murine mesenchymal stem cell line C3H/10T1/2. The results demonstrate successful on-command on/off switching of cell polarized motility and alignment. Decrease in fiber alignment causes a change from polarized motility along the direction of fiber alignment to non-polarized motility and from aligned to unaligned morphology, while increase in fiber alignment causes a change from non-polarized to polarized motility along the direction of fiber alignment and from unaligned to aligned morphology. In addition, the findings are consistent with the hypothesis that increased fiber alignment causes increased cell velocity, while decreased fiber alignment causes decreased cell velocity. On-command on/off switching of cell polarized motility and alignment is anticipated to enable new study of directed cell motility in tumor metastasis, in cell homing, and in tissue engineering.

Indexed as

Cell MovementAnimalsBiocompatible MaterialsCell LineCell Line, TumorCell NucleusCell PolarityCell ShapeExtracellular MatrixHumansMicePolymersStem CellsTissue ScaffoldsBiocompatible MaterialsPolymersCell alignmentDynamic architectural changeElectrospun scaffoldPolarized morphologyPolarized motilityShape memory polymer

Identifiers

PMID28649015
PMCPMC5577642
OpenAlexW2625303133

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.