Evidence map›Paper›PMID 33423407›Full record

ArticleJournal of biomedical optics2021

Visualization and quantification of pancreatic tumor stroma in fresh tissue via ultraviolet surface excitation.

Phuong Vincent, Petr Bruza, Scott M Palisoul, Jason R Gunn, Kimberley S Samkoe, P Jack Hoopes, Tayyaba Hasan, Brian W Pogue

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Critical PDT theory II: Current concepts and indications.Photodiagnosis and photodynamic therapy · 2022
    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

8 authors at 2 institutions in 1 country.

Phuong VincentDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Petr BruzaDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Scott M PalisoulDartmouth-Hitchock Pathology Shared Resource Lab, Lebanon, New Hampshire, United States.
Jason R GunnDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Kimberley S SamkoeDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
P Jack HoopesDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Tayyaba HasanHarvard Medical School, Wellman Center for Photomedicine, Boston, Massachusetts, United States.
Brian W PogueDartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Dartmouth College · USHarvard University · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Small Molecule Enhancers of Photodynamic Therapy for Skin CancerP01CA084203 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Brian William Pogue · 2001 to 2026
$27.9M
NCI NIH HHS P01 CA084203NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

significanceThe study has confirmed the feasibility of using ultraviolet (UV) excitation to visualize and quantify desmoplasia in fresh tumor tissue of pancreatic adenocarcinoma (PDAC) in an orthotopic xenograft mouse model, which provides a useful imaging platform to evaluate acute therapeutic responses.

aimStromal network of collagen prominent in PDAC tumors is examined by imaging fresh tissue samples stained with histological dyes. Fluorescence signals are color-transferred to mimic Masson's trichrome staining. APPROACH: Murine tumor samples were stained with Hoechst, eosin, and rhodamine B and excited at 275-nm. Fluorescence signals in the visible spectrum were captured by a CMOS color camera with high contrast and resolution at whole-tumor slice field of view.

resultsFluorescence imaging using UV excitation is capable of visualizing collagen deposition in PDAC tumors. Both fluorescence and histology data showed collagen content of up to 30%. The collagen modulation effect due to photodynamic priming treatment was observed showing 13% of collagen reduction. Necrosis area is visible and perfusion imaging using Texas Red dextran is feasible.

conclusionsThe study demonstrates collagen visualization in fresh PDAC tumor samples using UV excitation. This imaging platform also provides quantitative stromal information from fiber analysis and visibility of necrosis and perfusion, suitable for therapeutic response assessment of photodynamic therapy.

Indexed as

AdenocarcinomaPancreatic NeoplasmsPhotochemotherapyAnimalsCollagenMiceCollagencollagen imagingfluorescence imagingmicroscopy with ultraviolet surface excitationpancreatic adenocarcinomaphotodynamic therapyultraviolet light

Identifiers

PMID33423407
PMCPMC7850982
OpenAlexW3119486963

What OpenQuestion holds

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LicenceCC BY
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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.