Literature DB >> 3678576

Isolation and morphologic characterization of human ovarian carcinoma cell clusters present in effusions.

H J Allen1, C Porter, M Gamarra, M S Piver, E A Johnson.   

Abstract

Serous, mucinous, endometrioid and clear cell human ovarian carcinoma cells were isolated as multicellular aggregates from patient effusions by filtration on nylon mesh of defined porosity and examined by light microscopy. The cell clusters ranged from compact to loosely adherent groups of cells to spheroids with a central lumen surrounded by a cell monolayer. There was considerable variation in cluster morphology between effusions from different patients as well as within effusion from the same patient. Apparent budding of clusters was observed as well as different stages of cluster growth and development. This was observed for all histologic types studied. Electron microscopy of serous, mucinous and clear cell types showed that cells forming clusters were attached to each other by desmosomes, demonstrating that cluster formation did not result from a nonspecific stickiness of cells. Irregular microvilli were present on the external periphery of the various carcinoma cells and a prominent glycocalyx was present on the surface of mucinous carcinoma cells. Extensive interdigitation of cytoplasmic extensions and extended villi was present in mucinous and serous clusters which appeared to strengthen cluster cohesiveness. Nuclei were irregular with prominent nucleoli frequently present. The cell clusters usually remained intact and viable in culture but generally did not attach to glass or plastic substrata, whereas mesothelial cells and nonactivated histiocytes rapidly attached. When carcinoma cell clusters did attach, they were resistant to detachment by trypsin-EDTA treatment, in contrast to the nonmalignant cells.

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Year:  1987        PMID: 3678576     DOI: 10.1159/000163419

Source DB:  PubMed          Journal:  Exp Cell Biol        ISSN: 0304-3568


  23 in total

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2.  Initial formation of IGROV1 ovarian cancer multicellular aggregates involves vitronectin.

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3.  Combination of AKT inhibition with autophagy blockade effectively reduces ascites-derived ovarian cancer cell viability.

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4.  Mesothelial cells interact with tumor cells for the formation of ovarian cancer multicellular spheroids in peritoneal effusions.

Authors:  Isabelle Matte; Clara Major Legault; Perrine Garde-Granger; Claude Laplante; Paul Bessette; Claudine Rancourt; Alain Piché
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5.  Beta 1-integrins regulate the formation and adhesion of ovarian carcinoma multicellular spheroids.

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6.  Formation of stable small cell number three-dimensional ovarian cancer spheroids using hanging drop arrays for preclinical drug sensitivity assays.

Authors:  Shreya Raghavan; Maria R Ward; Katelyn R Rowley; Rachel M Wold; Shuichi Takayama; Ronald J Buckanovich; Geeta Mehta
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Review 7.  Three-dimensional modeling of ovarian cancer.

Authors:  Erin A White; Hilary A Kenny; Ernst Lengyel
Journal:  Adv Drug Deliv Rev       Date:  2014-07-14       Impact factor: 15.470

8.  Telomerase activity in human ovarian carcinoma.

Authors:  C M Counter; H W Hirte; S Bacchetti; C B Harley
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-12       Impact factor: 11.205

9.  Models of ovarian cancer metastasis: Murine models.

Authors:  Sanja Sale; Sandra Orsulic
Journal:  Drug Discov Today Dis Models       Date:  2006-06-01

Review 10.  Models for measuring metabolic chemical changes in the metastasis of high grade serous ovarian cancer: fallopian tube, ovary, and omentum.

Authors:  Hannah Lusk; Joanna E Burdette; Laura M Sanchez
Journal:  Mol Omics       Date:  2021-12-06
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