Evidence map›Paper›PMID 19819146›Full record

ReviewTrends in cell biology2009

Shining new light on 3D cell motility and the metastatic process.

Paolo P Provenzano, Kevin W Eliceiri, Patricia J Keely

Abstract readReview
In one paragraph

Review in Trends in cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Dynamics of 3D carcinoma cell invasion into aligned collagen.Integrative biology : quantitative biosciences from nano to macro · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Dual roles of CCN proteins in breast cancer progression.Journal of cell communication and signaling · 2016
    Article
  14. Article
  15. Article
  16. Review
  17. Periductal stromal collagen topology of pancreatic ductal adenocarcinoma differs from that of normal and chronic pancreatitis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
    Article
  18. Signaling networks that regulate cell migration.Cold Spring Harbor perspectives in biology · 2015
    Review
  19. Article
  20. Modeling persistence in mesenchymal cell motility using explicit fibers.Langmuir : the ACS journal of surfaces and colloids · 2014
    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

3 authors.

Paolo P ProvenzanoLaboratory for Optical and Computational Instrumentation, and Department of Biomedical Engineering, University of Wisconsin, Madison, WI, USA. ppproven@fhcrc.org
Kevin W Eliceiri
Patricia J Keely

Funding

Mechanisms Of Cell Migration On 3D Aligned MatricesR01CA142833 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI FRIEDL, ANDREAS, HAHN, KLAUS M. · 2010 to 2020
$3.4M
MOLECULAR MECHS REGULATING CANCER CELL PROLIFERATIONT32CA009681 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI HOFFMANN, F. MICHAEL · 1993 to 2007
$1.9M
A Spectral/Lifetime Microscope for in vivo StudiesR01EB000184 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI WHITE, JOHN GRAHAM · 2002 to 2006
$1.9M
R-Ras and Integrin Signaling in Breast Cell PhenotypeR01CA076537 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2003 to 2007
$1.8M
Biophysical Regulation of Breast DifferentiationR01CA114462 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2010 to 2014
$1.5M
Spectral/FLIM strategies for FRET based analysis of signal transduction pathwaysR21EB008811 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2009 to 2010
$398k
Using New Optical Techniques to Study Cell Signaling in 3D MatricesR21CA126635 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2008 to 2009
$323k
CDC42 AND INTEGRIN SIGNALING IN MAMMARY CELL PHENOTYPER29CA076537 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI KEELY, PATRICIA J · 1998 to 2002
$314k
NCI NIH HHS CA076537NCI NIH HHS R01 CA076537NCI NIH HHS R01 CA114462NCI NIH HHS R01 CA142833NCI NIH HHS R21 CA126635NCI NIH HHS R29 CA076537NCI NIH HHS T32 CA009681NCI NIH HHS T32CA009681NIBIB NIH HHS EB000184NIBIB NIH HHS R01 EB000184NIBIB NIH HHS R21 EB008811
6 · The paper itself

Abstract

Understanding tissue architecture and physical and chemical reciprocity between cells and their microenvironment provides vital insights into key events in cancer metastasis, such as cell migration through three-dimensional (3D) extracellular matrices. Yet, many mechanistic details associated with metastasis remain elusive due to the difficulty of studying cancer cells in relevant 3D microenvironments. Recently, optical imaging has facilitated the direct observation of single cells as they undertake fundamental steps in the metastatic processes. Optical imaging is also providing novel 'optical biomarkers' with diagnostic potential that are linked to cell-motility pathways associated with metastasis, and these can to help guide new approaches to cancer diagnosis and therapy. Here we present recent advances in one subclass of optical imaging of particular promise for cellular imaging - multiphoton microscopy - that can be used to improve the detection of malignant cells as well as advance our understanding of the cell biology of cancer metastasis.

Indexed as

Cell MovementAnimalsBiomarkers, TumorCytological TechniquesHumansImaging, Three-DimensionalMicroscopyNeoplasm MetastasisBiomarkers, Tumor

Identifiers

PMID19819146
PMCPMC2783928

What OpenQuestion holds

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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.