Evidence map›Paper›PMID 22961775›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2012

Multiphoton tomographic imaging: a potential optical biopsy tool for detecting gastrointestinal inflammation and neoplasia.

Tomoki Makino, Manu Jain, David C Montrose, Amit Aggarwal, Joshua Sterling, Brian P Bosworth, Jeffrey W Milsom, Brian D Robinson, Maria M Shevchuk, Kathy Kawaguchi and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  10. Stereotaxic device for optical imaging of mice hind feet.Journal of biomolecular techniques : JBT · 2013
    Article
  11. 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

17 authors at 1 institution in 1 country.

Tomoki MakinoDepartment of Medicine, Medical College of Cornell University, New York, NY 10065, USA.
Manu Jain
David C Montrose
Amit Aggarwal
Joshua Sterling
Brian P Bosworth
Jeffrey W Milsom
Brian D Robinson
Maria M Shevchuk
Kathy Kawaguchi
Ning Zhang
Christopher M Brown
David R Rivera
Wendy O Williams
Chris Xu
Andrew J Dannenberg
Sushmita Mukherjee
Cornell University · US

Funding

CANCER PHARMACOLOGYT32CA062948 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LORRAINE J GUDAS · 1994 to 2026
$12.1M
Development of Medical Multiphoton Microscopic EndoscopyR01EB006736 · NIBIB · CORNELL UNIVERSITY · PI WEBB, WATT W · 2007 to 2011
$5.3M
Academic-industrial partnership for development of in vivo imaging systems and meR01CA133148 · NCI · CORNELL UNIVERSITY · PI GRUNER-NIELSEN, LARS, XU, CHRIS · 2008 to 2011
$1.8M
NCI NIH HHS R01 CA133148NCI NIH HHS R01-CA133148NCI NIH HHS T32 CA062948NIBIB NIH HHS R01 EB006736NIBIB NIH HHS R01-EB006736
6 · The paper itself

Abstract

Endoscopy is widely used to detect and remove premalignant lesions with the goal of preventing gastrointestinal (GI) cancers. Because current endoscopes do not provide cellular resolution, all suspicious lesions are biopsied and subjected to histologic evaluation. Technologies that facilitate directed biopsies should decrease both procedure-related morbidity and cost. Here we explore the use of multiphoton microscopy (MPM), an optical biopsy tool that relies on intrinsic tissue emissions, to evaluate pathology in both experimental and human GI specimens, using hematoxylin and eosin (H&E)-stained sections from these tissues for comparison. After evaluating the entire normal mouse GI tract, MPM was used to investigate disease progression in mouse models of colitis and colorectal carcinogenesis. MPM provided sufficient histologic detail to identify all relevant substructures in ex vivo normal GI tissue, visualize both acute and resolving stages of colitis, and show the progression of colorectal carcinogenesis. Next, ex vivo specimens from human subjects with celiac sprue, inflammatory bowel disease, and colorectal neoplasia were imaged by MPM. Finally, colonic mucosa in live anesthetized rats was imaged in vivo using a flexible endoscope prototype. In both animal models and human specimens, MPM images showed a striking similarity to the results of H&E staining, as shown by the 100% concordance achieved by the study pathologists' diagnoses. In summary, MPM is a promising technique that accurately visualizes histology in fresh, unstained tissues. Our findings support the continued development of MPM as a technology to enhance the early detection of GI pathologies including premalignant lesions.

Indexed as

AnimalsBiopsyCarcinomaDisease ProgressionGastrointestinal NeoplasmsHumansInflammationInflammatory Bowel DiseasesMaleMiceMice, Inbred C57BLMicroscopy, Fluorescence, MultiphotonRatsRats, Sprague-DawleySurgery, Computer-AssistedTomography

Identifiers

PMID22961775
PMCPMC3491145
OpenAlexW2103906715

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.