Evidence map›Paper›PMID 18986607›Full record

ArticleMicroscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada2008

Nonlinear optical imaging of cellular processes in breast cancer.

Paolo P Provenzano, Kevin W Eliceiri, Long Yan, Aude Ada-Nguema, Matthew W Conklin, David R Inman, Patricia J Keely

Abstract read
In one paragraph

Article in Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada, 2008. 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
3.3field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  7. Review
  8. Transfer of assembled collagen fibrils to flexible substrates for mechanically tunable contact guidance cues.Integrative biology : quantitative biosciences from nano to macro · 2018
    Article
  9. Article
  10. Article
  11. Methods for Quantifying Fibrillar Collagen Alignment.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  12. Oriented collagen fibers direct tumor cell intravasation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
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  17. Review
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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

7 authors at 3 institutions in 1 country.

Paolo P ProvenzanoDepartment of Pharmacology, University of Wisconsin, Madison, WI 53706, USA.
Kevin W Eliceiri
Long Yan
Aude Ada-Nguema
Matthew W Conklin
David R Inman
Patricia J Keely
University of Wisconsin–Madison · USUniversity of Wisconsin System · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

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
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 R29 CA076537NIBIB NIH HHS R01 EB000184
6 · The paper itself

Abstract

Nonlinear optical imaging techniques such as multiphoton and second harmonic generation (SHG) microscopy used in conjunction with novel signal analysis techniques such as spectroscopic and fluorescence excited state lifetime detection have begun to be used widely for biological studies. This is largely due to their promise to noninvasively monitor the intracellular processes of a cell together with the cell's interaction with its microenvironment. Compared to other optical methods these modalities provide superior depth penetration and viability and have the additional advantage in that they are compatible technologies that can be applied simultaneously. Therefore, application of these nonlinear optical approaches to the study of breast cancer holds particular promise as these techniques can be used to image exogeneous fluorophores such as green fluorescent protein as well as intrinsic signals such as SHG from collagen and endogenous fluorescence from nicotinamide adenine dinucleotide or flavin adenine dinucleotide. In this article the application of multiphoton excitation, SHG, and fluorescence lifetime imaging microscopy to relevant issues regarding the tumor-stromal interaction, cellular metabolism, and cell signaling in breast cancer is described. Furthermore, the ability to record and monitor the intrinsic fluorescence and SHG signals provides a unique tool for researchers to understand key events in cancer progression in its natural context.

Indexed as

Microscopy, Fluorescence, MultiphotonAnimalsBreast NeoplasmsCell Line, TumorCell Physiological PhenomenaChlorocebus aethiopsCOS CellsFemaleHumansMiceSignal Transduction

Identifiers

PMID18986607
PMCPMC5575804
OpenAlexW2145675587

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.