Literature DB >> 11572092

Characterization of cultured human prostatic epithelial cells by cluster designation antigen expression.

A Y Liu1, D M Peehl.   

Abstract

Cultured prostatic epithelial cells have been extensively studied as a model of prostate biology. What is the lineage relationship of the cultured cells to the epithelial cell types in tissue? How different are cultured cells derived from tumor tissue to those derived from benign tissue? Expression of cluster designation (CD) cell surface molecules has been shown to be useful in characterizing cells according to lineage. A CD profile was therefore generated for cultured human prostatic epithelial cells and compared with those previously established for basal and luminal epithelial cells in the prostate. Presence of CD44, CD49b, CD49f, and CD104 and absence of CD57 suggests that cultured cells were derived from basal cells of prostatic tissues. However, expression of certain CD antigens characteristic of luminal epithelial cells was also observed in subpopulations of cultured cells. The pattern of CD antigens in cultured cells reflects a phenotype similar to that of transit-amplifying cells that have been described in the prostate. Several CD antigens were found expressed by both cultured prostatic epithelial and stromal cells, and are probably associated with cell proliferation. The CD profiles of cultured epithelial cell strains derived from normal compared with malignant tissues were notably similar to each other and to that of the prostate cancer cell line PC-3. We conclude that cells in culture retain expression of certain lineage-characteristic CD antigens. Furthermore, CD antigens can define subpopulations of cells with differential gene expression.

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Year:  2001        PMID: 11572092     DOI: 10.1007/s004410100419

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  9 in total

1.  Characterization of prostate cell types by CD cell surface molecules.

Authors:  Alvin Y Liu; Lawrence D True
Journal:  Am J Pathol       Date:  2002-01       Impact factor: 4.307

2.  Expression of the IGF axis is decreased in local prostate cancer but enhanced after benign prostate epithelial differentiation and TGF-β treatment.

Authors:  Petra Massoner; Michael Ladurner Rennau; Isabel Heidegger; Anita Kloss-Brandstätter; Monika Summerer; Eva Reichhart; Georg Schäfer; Helmut Klocker
Journal:  Am J Pathol       Date:  2011-10-06       Impact factor: 4.307

Review 3.  Reprogramming of prostate cancer cells--technical challenges.

Authors:  Gisely T Borges; Eneida F Vêncio; Ricardo Z N Vêncio; Robert L Vessella; Carol B Ware; Alvin Y Liu
Journal:  Curr Urol Rep       Date:  2015-01       Impact factor: 3.092

4.  Heterogeneity in primary and metastatic prostate cancer as defined by cell surface CD profile.

Authors:  Alvin Y Liu; Martine P Roudier; Lawrence D True
Journal:  Am J Pathol       Date:  2004-11       Impact factor: 4.307

Review 5.  Exploring the origins of the normal prostate and prostate cancer stem cell.

Authors:  Susan Kasper
Journal:  Stem Cell Rev       Date:  2008-09       Impact factor: 5.739

6.  Inhibition of monoamine oxidase A promotes secretory differentiation in basal prostatic epithelial cells.

Authors:  Hongjuan Zhao; Rosalie Nolley; Zuxiong Chen; Stephen W Reese; Donna M Peehl
Journal:  Differentiation       Date:  2008-01-31       Impact factor: 3.880

7.  Correlation of mRNA and protein levels: cell type-specific gene expression of cluster designation antigens in the prostate.

Authors:  Laura E Pascal; Lawrence D True; David S Campbell; Eric W Deutsch; Michael Risk; Ilsa M Coleman; Lillian J Eichner; Peter S Nelson; Alvin Y Liu
Journal:  BMC Genomics       Date:  2008-05-23       Impact factor: 3.969

8.  Molecular signaling pathways mediating osteoclastogenesis induced by prostate cancer cells.

Authors:  Shahrzad Rafiei; Svetlana V Komarova
Journal:  BMC Cancer       Date:  2013-12-26       Impact factor: 4.430

Review 9.  Prostate Cancer Stem Cells: Research Advances.

Authors:  Dagmara Jaworska; Wojciech Król; Ewelina Szliszka
Journal:  Int J Mol Sci       Date:  2015-11-17       Impact factor: 5.923

  9 in total

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