Engineering fibrotic tissue in pancreatic cancer

A novel three-dimensional model to investigate nanoparticle delivery

Hitomi Hosoya, Koji Kadowaki, Michiya Matsusaki, Horacio Cabral, Hiroshi Nishihara, Hideaki Ijichi, Kazuhiko Koike, Kazunori Kataoka, Kohei Miyazono, Mitsuru Akashi, Mitsunobu R. Kano

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Pancreatic cancer contains both fibrotic tissue and tumor cells with embedded vasculature. Therefore anti-cancer nanoparticles need to extravasate from tumor vasculature and permeate thick fibrotic tissue to target tumor cells. To date, permeation of drugs has been investigated in vitro using monolayer models. Since three-dimensional migration of nanoparticles cannot be analyzed in a monolayer model, we established a novel, three-dimensional, multilayered, in vitro model of tumor fibrotic tissue, using our hierarchical cell manipulation technique with K643f fibroblasts derived from a murine pancreatic tumor model. NIH3T3 normal fibroblasts were used in comparison. We analyzed the size-dependent effect of nanoparticles on permeation in this experimental model using fluorescent dextran molecules of different molecular weights. The system revealed permeation decreased as number of layers of cultured cells increased, or as molecule size increased. Furthermore, we showed changes in permeation depended on the source of the fibroblasts. Observations of this sort cannot be made in conventional monolayer culture systems. Thus our novel technique provides a promising in vitro means to investigate permeation of nanoparticles in fibrotic tissue, when both type and number of fibroblasts can be regulated.

Original languageEnglish
Pages (from-to)32-37
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume419
Issue number1
DOIs
Publication statusPublished - 2012 Mar 2
Externally publishedYes

Fingerprint

Tissue Engineering
Pancreatic Neoplasms
Tissue engineering
Permeation
Nanoparticles
Tumors
Fibroblasts
Tissue
Monolayers
Cells
Neoplasms
Molecules
Dextrans
Molecular weight
Cultured Cells
Theoretical Models
Molecular Weight
Pharmaceutical Preparations
In Vitro Techniques

Keywords

  • Fibroblasts
  • Fibrosis
  • NanoDDS
  • Pancreatic cancer
  • Permeability

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Engineering fibrotic tissue in pancreatic cancer : A novel three-dimensional model to investigate nanoparticle delivery. / Hosoya, Hitomi; Kadowaki, Koji; Matsusaki, Michiya; Cabral, Horacio; Nishihara, Hiroshi; Ijichi, Hideaki; Koike, Kazuhiko; Kataoka, Kazunori; Miyazono, Kohei; Akashi, Mitsuru; Kano, Mitsunobu R.

In: Biochemical and Biophysical Research Communications, Vol. 419, No. 1, 02.03.2012, p. 32-37.

Research output: Contribution to journalArticle

Hosoya, H, Kadowaki, K, Matsusaki, M, Cabral, H, Nishihara, H, Ijichi, H, Koike, K, Kataoka, K, Miyazono, K, Akashi, M & Kano, MR 2012, 'Engineering fibrotic tissue in pancreatic cancer: A novel three-dimensional model to investigate nanoparticle delivery', Biochemical and Biophysical Research Communications, vol. 419, no. 1, pp. 32-37. https://doi.org/10.1016/j.bbrc.2012.01.117
Hosoya, Hitomi ; Kadowaki, Koji ; Matsusaki, Michiya ; Cabral, Horacio ; Nishihara, Hiroshi ; Ijichi, Hideaki ; Koike, Kazuhiko ; Kataoka, Kazunori ; Miyazono, Kohei ; Akashi, Mitsuru ; Kano, Mitsunobu R. / Engineering fibrotic tissue in pancreatic cancer : A novel three-dimensional model to investigate nanoparticle delivery. In: Biochemical and Biophysical Research Communications. 2012 ; Vol. 419, No. 1. pp. 32-37.
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