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Immunohistochemical analysis of differentiation in static and mixed prostate cancer spheroids
Author(s) -
Song Hong,
O'Connor Kim C.,
David Odile,
Giordano Carrie L.,
PappasLeBeau Helena,
Clejan Sanda
Publication year - 2003
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/j.1582-4934.2003.tb00217.x
Subject(s) - spheroid , cytokeratin , lncap , immunohistochemistry , cellular pathology , prostate cancer , pathology , extracellular matrix , biology , multicellular organism , cancer research , prostate , cellular differentiation , phenotype , microbiology and biotechnology , in vitro , cancer , cell , immunology , medicine , biochemistry , genetics , gene
Neoplastic multicellular spheroids are in vitro models of solid tumors employed in drug testing and basic research. This study compares differentiation in static and mixed prostate cancer spheroids. Staining intensity of prostate specific antigen (PSA) was down‐regulated upon mixing from 0.21 ± 0.03 to 0.13 ± 0.03 in LNCaP multicellular spheroids, and from 0.13 ± 0.04 to 0.03 ± 0.02 in DU 145 multicellular spheroids. This was accompanied by 65% increase in the expression of cytokeratins 8 and 18 in DU 145 spheroids. PSA expression extended 60 μm within static spheroids and was disrupted in mixed culture. Diminished PSA expression and spatial organization suggests a more aggressive cancer. Higher cytokeratin expression could result from either differentiation towards a luminal phenotype or activation of the Ras pathway during dedifferentiation. THus, the existing paradigm of differentiation established for normal tissue does not apply for our neoplastic spheroids. Cell dedifferentiation is attributed to improved interstitial transport and synthesis of extracellular matrix.

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