Literature DB >> 3800336

Ultrastructural analysis of experimentally induced invasion in the rat lung by tumor cells metastasizing lymphatically.

S Paku, N Paweletz, E Spiess, P Aulenbacher, H O Werling, M Knierim.   

Abstract

The colonization of the lung by the rat tumor cells BSp73 ASML which have the ability to metastasize via the lymphatic system was studied at the ultrastructural level. Tumor cells arriving in the lung after i.v. injection become transiently embolized; within hours, however, they begin to extravasate from the blood capillaries. Swelling cellular protrusions open a limited area between endothelium and basal lamina through which tumor cells erupt. Tumor cells then form metastases in the interstitial tissue and, in an apparently lymphotropic action, intravasate the lymphatic vessels in a similar manner to a reverse diapedesis-like process. Within the lympatic system they settle, spread, and build up extensive tumor foci particularly in the subpleural region.

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Year:  1986        PMID: 3800336

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  4 in total

1.  Organ-specificity of the extravasation process: an ultrastructural study.

Authors:  S Paku; B Döme; R Tóth; J Timár
Journal:  Clin Exp Metastasis       Date:  2000       Impact factor: 5.150

2.  Ultrastructure of invasion in different tissue types by Lewis lung tumour variants.

Authors:  S Paku; J Timár; K Lapis
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

3.  Endothelialization of embolized tumor cells during metastasis formation.

Authors:  K Lapis; S Paku; L A Liotta
Journal:  Clin Exp Metastasis       Date:  1988 Jan-Feb       Impact factor: 5.150

4.  Tumor cell motility and metastasis : Autocrine motility factor as an example of ecto/exoenzyme cytokines.

Authors:  S Silletti; S Paku; A Raz
Journal:  Pathol Oncol Res       Date:  1997-09       Impact factor: 3.201

  4 in total

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