Published March 17, 2020 | Version v1
Dataset Open

Dataset related to article "Computer-aided assessment of the extra-cellular matrix during pancreatic carcinogenesis: a pilot study."

  • 1. Humanitas Clinical and Research Center – IRCCS -, via Manzoni 56, 20089 Rozzano (Mi) - Italy AND Humanitas University, Department of Biomedical Sciences, Via Rita Levi Montalcini 4, 20090 Pieve Emanuele – Milan, Italy
  • 2. Internal Medicine Unit, Maggiore Hospital, Bologna, Italy.
  • 3. Humanitas Clinical and Research Center – IRCCS -, via Manzoni 56, 20089 Rozzano (Mi) - Italy
  • 4. Anatomic Pathology Service, Maggiore Hospital, Bologna, Italy.
  • 5. "Michele Rodriguez" Foundation-Institute for Quantitative Measures in Medicine, Milan, Italy.
  • 6. Department of Pharmacy and Biotechnology (FaBiT), University of Bologna, Bologna, Italy.
  • 7. Surgery Unit, Maggiore Hospital, Bologna, Italy.
  • 8. Ultrasound Center Internal Medicine A, Maggiore Hospital, Bologna, Italy.
  • 9. CNR Institute of Neuroscience, Padua, Italy.
  • 10. Kiromic Biopharma, Inc., Houston, TX, USA.
  • 11. Department of Gastroenterology, Hepatology & Nutrition, Division of Internal Medicine, The University of Texas MD Anderson Cancer, Houston, TX, USA.

Description

BACKGROUND:

A hallmark of pancreatic ductal adenocarcinoma is the desmoplastic reaction, but its impact on the tumor behavior remains controversial. Our aim was to introduce a computer -aided method to precisely quantify the amount of pancreatic collagenic extra-cellular matrix, its spatial distribution pattern, and the degradation process.

METHODS:

A series of normal, inflammatory and neoplastic pancreatic ductal adenocarcinoma formalin-fixed and paraffin-embedded Sirius red stained sections were automatically digitized and analyzed using a computer-aided method.

RESULTS:

We found a progressive increase of pancreatic collagenic extra-cellular matrix from normal to the inflammatory and pancreatic ductal adenocarcinoma. The two-dimensional fractal dimension showed a significant difference in the collagenic extra-cellular matrix spatial complexity between normal versus inflammatory and pancreatic ductal adenocarcinoma. A significant difference when comparing the number of cycles necessary to degrade the pancreatic collagenic extra-cellular matrix in normal versus inflammatory and pancreatic ductal adenocarcinoma was also found. The difference between inflammatory and pancreatic ductal adenocarcinoma was also significant. Furthermore, the mean velocity of collagenic extra-cellular matrix degradation was found to be faster in inflammatory and pancreatic ductal adenocarcinoma than in normal.

CONCLUSION:

These findings demonstrate that inflammatory and pancreatic ductal adenocarcinomas are characterized by an increased amount of pancreatic collagenic extra-cellular matrix and by changes in their spatial complexity and degradation. Our study defines new features about the pancreatic collagenic extra-cellular matrix, and represents a basis for further investigations into the clinical behavior of pancreatic ductal adenocarcinoma and the development of therapeutic strategies.

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Additional details

Related works

Is supplement to
3081-9202 (ISSN)
10.1186/s12967-019-1817-3 (DOI)