Evidence map›Paper›PMID 40210130›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2025

Polychromatic Polarization Microscopy Differentiates Collagen Fiber Signatures in Benign Pancreatic Tissue and Pancreatic Ductal Adenocarcinoma.

Mahsa Chitsaz, Linlin Yang, Rania Rayes-Danan, Omid Savari, Bin Li, Michael Shribak, Kevin Eliceiri, Agnes Loeffler

Abstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Mahsa ChitsazDepartment of Pathology, Cleveland Clinic Foundation, Cleveland, Ohio.
Linlin YangDepartment of Pathology, Cleveland Clinic Foundation, Cleveland, Ohio.
Rania Rayes-DananDepartment of Pathology, MetroHealth Medical Center, Cleveland, Ohio.
Omid SavariDepartment of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
Bin LiDepartment of Engineering Science, University of Oxford, Oxford, United Kingdom.
Michael ShribakMarine Biological Laboratory, Woods Hole, Massachusetts.
Kevin EliceiriCenter for Quantitative Cell Imaging, University of Wisconsin, Madison, Wisconsin; Morgridge Institute for Research, Madison, Wisconsin.
Agnes LoefflerDepartment of Pathology, MetroHealth Medical Center, Cleveland, Ohio. Electronic address: aloeffler@metrohealth.org.

Funding

TECH CoreU54CA268069 · NCI · UNIVERSITY OF MINNESOTA · PI David J. Odde · 2022 to 2026
$8.2M
The Center for Label-free Imagingand Multiscale Biophotonics (CLIMB)P41EB031772 · NIBIB · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Stephen A Boppart · 2022 to 2026
$7.6M
Orientation Independent DIC and Polarization MicroscopyR01GM101701 · NIGMS · MARINE BIOLOGICAL LABORATORY · PI SHRIBAK, MICHAEL · 2012 to 2020
$3.8M
NCI NIH HHS U54 CA268069NIBIB NIH HHS P41 EB031772NIGMS NIH HHS R01 GM101701
6 · The paper itself

Abstract

The orientation of collagen fibers in relation to malignant epithelium is known to carry prognostic information in a variety of tissues. The data are the strongest for breast and pancreatic ductal adenocarcinoma. However, information inherent in collagen fiber topology in malignant tissues remains untapped in daily surgical pathology practice, largely because collagen fibers within areas of desmoplasia cannot be resolved with standard diagnostic microscopy. The methodologies used to visualize collagen fiber orientation are either of insufficient resolution to consistently capture collagen fiber topology or require resources in time and money that do not fit into the daily surgical pathology workflow. Polychromatic polarization microscopy has the potential to bring collagen topology to the attention of pathologists during their routine work. It has been demonstrated to be equivalent to the gold standard methodology used to research collagen, second harmonic generation. We use polychromatic polarization microscopy to visualize and describe the differences in collagen topology in normal pancreas, chronic pancreatitis, and pancreatic ductal adenocarcinoma with a standard microscope, using hematoxylin and eosin-stained sections. In the process, we propose a lexicon with which to describe the morphologic characteristics of collagen in benign and malignant pancreatic tissues.

Indexed as

Carcinoma, Pancreatic DuctalCollagenPancreasPancreatic NeoplasmsPancreatitis, ChronicHumansMicroscopy, PolarizationCollagencollagendesmoplasiapancreatic ductal adenocarcinomapolychromatic polarization microscopy

Identifiers

PMID40210130
PMCPMC12767205

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.