Literature DB >> 10359532

C-CAM1 expression: differential effects on morphology, differentiation state and suppression of human PC-3 prostate carcinoma cells.

M M Comegys1, M P Carreiro, J F Brown, A Mazzacua, D L Flanagan, A Makarovskiy, S H Lin, D C Hixson.   

Abstract

Studies in rat prostate and liver have suggested that C-CAM1 is involved in the formation and maintenance of histotypic associations in tissues and possibly tumors. Most recently, C-CAM1 has been shown to suppress tumorigenicity of prostate and colon carcinoma cells. However, the mechanisms whereby C-CAM1 suppresses growth and the relationship of this activity to its proposed role in histotypic interactions remain largely unknown. In the present study, we have analysed the growth, phenotypic, morphological and ultrastructural characteristics of four human PC-3 prostate carcinoma cell lines transduced with C-CAM1 retrovirus. We report that three of four lines regained their tumorigenic phenotype in vivo while maintaining high levels of C-CAM1 expression and a growth retarded phenotype in vitro. These findings suggested that high levels of C-CAM1 expression were negatively influencing recovery during reconstitution after freezing or during the latency period after subcutaneous injection and that loss of suppression resulted from changes in expression of other molecules required for full disclosure of C-CAM1 mediated growth inhibition. Results from Northern blot and immunofluorescence analyses of tumor nodules demonstrated that C-CAM1 decreased rather than enhanced phenotypic differentiation and induced ultrastructural and morphological changes that occurred independently of tumor suppression.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10359532     DOI: 10.1038/sj.onc.1202666

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  5 in total

1.  Endogenous and transplanted small hepatocytes in retrorsine-treated/partially hepatectomized rat liver show differences in growth, phenotype, and proximity to clusters of gamma-glutamyl transpeptidase-positive host hepatocytes.

Authors:  Chise Tateno; Marie P Carreiro; Douglas C Hixson
Journal:  J Histochem Cytochem       Date:  2009-09-28       Impact factor: 2.479

2.  Engraftment of syngeneic and allogeneic endothelial cells, hepatocytes and cholangiocytes into partially hepatectomized rats previously treated with mitomycin C.

Authors:  Kate E Brilliant; David R Mills; Helen M Callanan; Douglas C Hixson
Journal:  Transplantation       Date:  2009-08-27       Impact factor: 4.939

3.  Direct interaction of tumor suppressor CEACAM1 with beta catenin: identification of key residues in the long cytoplasmic domain.

Authors:  Lan Jin; Yun Li; Charng-Jui Chen; Mark A Sherman; Keith Le; John E Shively
Journal:  Exp Biol Med (Maywood)       Date:  2008-04-29

4.  The transmembrane domain of CEACAM1-4S is a determinant of anchorage independent growth and tumorigenicity.

Authors:  Erica L Lawson; David R Mills; Kate E Brilliant; Douglas C Hixson
Journal:  PLoS One       Date:  2012-01-03       Impact factor: 3.240

5.  Role of CEACAM1 and CEACAM20 in an in vitro model of prostate morphogenesis.

Authors:  Hui Zhang; Andreas Eisenried; Wolfgang Zimmermann; John E Shively
Journal:  PLoS One       Date:  2013-01-24       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.