Literature DB >> 8919352

Computer simulation modelling and visualization of 3D architecture of biological tissues. Simulation of the evolution of normal, metaplastic and dysplastic states of the nasal epithelium.

C J Clem1, J P Rigaut.   

Abstract

Recent technical improvements, such as 3D microscopy imaging, have shown the necessity of studying 3D biological tissue architecture during carcinogenesis. In the present paper a computer simulation model is developed allowing the visualization of the microscopic biological tissue architecture during the development of metaplastic and dysplastic lesions. The static part of the model allows the simulation of the normal, metaplastic and dysplastic architecture of an external epithelium. This model is associated to a knowledge base which contains only data on the nasal epithelium. The latter has been well studied by numerous authors and its lesional states are well known. An inference engine allows the initialization of the static model parameters. A statistical comparison between simulated epithelia and real epithelia is achieved by adjusting the parameter values during the simulation. The dynamic part of the model allows the simulation of a growth process on a 3D representation based on the static model. The main hypothesis is that nasal epithelium is submitted to a continuous transformation from normal to cancer through metaplasia and dysplasia. The evolution of each cell (represented by its nucleus) depends on its local environment and also on its heritage from its mother-cell. Simulation of tissue renewal of the nasal pseudostratified epithelium has been achieved. The evolution from normal to hyperplasia has been simulated. After modification of the cell cycle modelling, the simulation of the development of metaplastic foci has been obtained.

Entities:  

Mesh:

Year:  1995        PMID: 8919352     DOI: 10.1007/bf00713563

Source DB:  PubMed          Journal:  Acta Biotheor        ISSN: 0001-5342            Impact factor:   1.774


  68 in total

Review 1.  On the generation of form by the continuous interactions between cells and their extracellular matrix.

Authors:  L Ettinger; F Doljanski
Journal:  Biol Rev Camb Philos Soc       Date:  1992-11

2.  A minimal cascade model for the mitotic oscillator involving cyclin and cdc2 kinase.

Authors:  A Goldbeter
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-15       Impact factor: 11.205

3.  Cell migration velocities in the crypts of the small intestine after cytotoxic insult are not dependent on mitotic activity.

Authors:  P Kaur; C S Potten
Journal:  Cell Tissue Kinet       Date:  1986-11

4.  A morphometric model for light microscopic analysis of metaplastic, dysplastic, and carcinomatous alterations of the nasal mucosa in nickel workers.

Authors:  M Boysen; A Reith
Journal:  Pathol Res Pract       Date:  1980       Impact factor: 3.250

5.  Autoradiographic cytokinetics of colonic mucosal hyperplasia in mice.

Authors:  S W Barthold
Journal:  Cancer Res       Date:  1979-01       Impact factor: 12.701

6.  Discrimination of various epithelia by simple morphometric evaluation of the basal cell layer. A light microscopic analysis of pseudostratified, metaplastic and dysplastic nasal epithelium in nickel workers.

Authors:  M Boysen; A Reith
Journal:  Virchows Arch B Cell Pathol Incl Mol Pathol       Date:  1983

Review 7.  Tumors as caricatures of the process of tissue renewal: prospects for therapy by directing differentiation.

Authors:  G B Pierce; W C Speers
Journal:  Cancer Res       Date:  1988-04-15       Impact factor: 12.701

8.  Histopathologic changes of nasal mucosa in nickel workers: a pilot study.

Authors:  W Torjussen; L A Solberg; A C Høgetveit
Journal:  Cancer       Date:  1979-09       Impact factor: 6.860

9.  Regional increases in rat nasal epithelial cell proliferation following acute and subchronic inhalation of formaldehyde.

Authors:  T M Monticello; F J Miller; K T Morgan
Journal:  Toxicol Appl Pharmacol       Date:  1991-12       Impact factor: 4.219

10.  Contact stimulation of cell migration.

Authors:  L A Thomas; K M Yamada
Journal:  J Cell Sci       Date:  1992-12       Impact factor: 5.285

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