Evidence map›Paper›PMID 33672734›Full record

ArticleCancers2021

Morphological Heterogeneity in Pancreatic Cancer Reflects Structural and Functional Divergence.

Petra Sántha, Daniela Lenggenhager, Anette Finstadsveen, Linda Dorg, Kristin Tøndel, Manoj Amrutkar, Ivar P Gladhaug, Caroline Verbeke

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  15. MRI Radiogenomics in Precision Oncology: New Diagnosis and Treatment Method.Computational intelligence and neuroscience · 2022
    Review
  16. Article
  17. 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.

Petra SánthaDepartment of Pathology, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.
Daniela LenggenhagerDepartment of Pathology and Molecular Pathology, University Hospital Zürich, University of Zürich, 8091 Zürich, Switzerland.
Anette FinstadsveenDepartment of Pathology, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.
Linda DorgDepartment of Pathology, Institute of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.
Kristin TøndelDepartment of Data Science, Faculty of Science and Technology, Norwegian University of Life Sciences, 1430 Ås, Norway.
Manoj AmrutkarDepartment of Pathology, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.ORCID 0000-0002-1868-0249
Ivar P GladhaugDepartment of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.
Caroline VerbekeDepartment of Pathology, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.ORCID 0000-0002-1111-9715

Funding

Helse Sør-Øst RHF 2016090Kreftforeningen 212734-2019
6 · The paper itself

Abstract

Inter- and intratumor heterogeneity is an important cause of treatment failure. In human pancreatic cancer (PC), heterogeneity has been investigated almost exclusively at the genomic and transcriptional level. Morphological heterogeneity, though prominent and potentially easily assessable in clinical practice, remains unexplored. This proof-of-concept study aims at demonstrating that morphological heterogeneity reflects structural and functional divergence. From the wide morphological spectrum of conventional PC, four common and distinctive patterns were investigated in 233 foci from 39 surgical specimens. Twenty-six features involved in key biological processes in PC were analyzed (immuno-)histochemically and morphometrically: cancer cell proliferation (Ki67) and migration (collagen fiber alignment, MMP14), cancer stem cells (CD44, CD133, ALDH1), amount, composition and spatial arrangement of extracellular matrix (epithelial proximity, total collagen, collagen I and III, fibronectin, hyaluronan), cancer-associated fibroblasts (density, αSMA), and cancer-stroma interactions (integrins α2, α5, α1; caveolin-1). All features differed significantly between at least two of the patterns. Stromal and cancer-cell-related features co-varied with morphology and allowed prediction of the morphological pattern. In conclusion, morphological heterogeneity in the cancer-cell and stromal compartments of PC correlates with structural and functional diversity. As such, histopathology has the potential to inform on the operationality of key biological processes in individual tumors.

Indexed as

extracellular matrixheterogeneityhuman pancreatic ductal adenocarcinomamorphologypathologystroma

Identifiers

PMID33672734
PMCPMC7924365

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Registered trials

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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.