Evidence map›Paper›PMID 19964821›Full record

ArticleAnnual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference2009

Nonlinear optical microscopy and computational analysis of intrinsic signatures in breast cancer.

Curtis T Rueden, Matthew W Conklin, Paolo P Provenzano, Patricia J Keely, Kevin W Eliceiri

Open access · greenAbstract read
In one paragraph

Article in Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.4field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  8. Cellular imaging in rheumatic diseases.Nature reviews. Rheumatology · 2015
    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

5 authors at 2 institutions in 1 country.

Curtis T RuedenLaboratory for Optical and Computational Instrumentation, University of Wisconsin, Madison, WI 53706 USA. ctrueden@wisc.edu
Matthew W Conklin
Paolo P Provenzano
Patricia J Keely
Kevin W Eliceiri
University of Wisconsin–Madison · USOptica · 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
Spectral/FLIM strategies for FRET based analysis of signal transduction pathwaysR21EB008811 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2009 to 2010
$398k
NCI NIH HHS R01 CA076537NCI NIH HHS R01-CA076537NIBIB NIH HHS R01 EB000184NIBIB NIH HHS R01-EB000184NIBIB NIH HHS R21 EB008811
6 · The paper itself

Abstract

Recently, new non-invasive imaging methods have been developed and applied to cellular and animal mammary models that have enabled breast cancer researchers to track key players and events in mammary metastasis. Noninvasive nonlinear optical methods such as multiphoton laser scanning microscopy (MPLSM), Fluorescence Lifetime Microscopy (FLIM) and second harmonic generation (SHG) imaging provide an unrivaled ability for obtaining high-resolution images from deep within tissue that can be exploited in the quest to understand breast cancer progression. These optical methods can add greatly to our knowledge of cancer progression by allowing key processes to be non-invasively imaged such as metabolism (on the basis of free and bound NADH detection via FLIM) and interactions with the extracellular matrix (SHG imaging of collagen). In this short application note we present a survey of our latest optical and computational efforts to study intrinsic fluorescence in breast cancer models. In particular we present the latest development in our SLIM Plotter application, an open source visualization program for interactive visualization and inspection of combined spectral lifetime (SLIM) data.

Indexed as

AlgorithmsBreast NeoplasmsCollagenDisease ProgressionEquipment DesignHumansImage Processing, Computer-AssistedMicroscopyMicroscopy, FluorescenceNADNeoplasm MetastasisOptics and PhotonicsProgramming LanguagesSoftwareCollagenNAD

Identifiers

PMID19964821
PMCPMC6016541
OpenAlexW2109167698

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.