Literature DB >> 10512760

The cytoplasmic domain of C-CAM1 tumor suppressor is necessary and sufficient for suppressing the tumorigenicity of prostate cancer cells.

V T Estrera1, W Luo, D Phan, K Earley, D C Hixson, S H Lin.   

Abstract

We have previously shown that C-CAM1 cell adhesion molecule can suppress the growth of prostate cancer cells in vivo. In this study, we determined the minimal domain of C-CAM1 that is required for its tumor-suppressive activity. DU145 prostate cancer cells were infected with recombinant adenoviruses containing various C-CAM1 mutant genes, and the effects of the mutant C-CAM1 proteins on the growth of DU145 cells were assessed in a nude-mice xenograft model. Deletion of C-CAM1's cytoplasmic domain, which is not required for its adhesion activity, abolished the growth-suppressive activity, whereas deletion of the adhesion domain did not. This observation suggests that C-CAM1's extracellular domain may be not essential for its tumor suppressive activity. Indeed, we found that expression of the C-CAM1 cytoplasmic domain alone led to growth suppression of DU145 cells. These results suggest that the cytoplasmic domain of C-CAM1 is necessary and sufficient for its growth-suppressive function. Copyright 1999 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10512760     DOI: 10.1006/bbrc.1999.1443

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Differences in tissue-specific and embryonic expression of mouse Ceacam1 and Ceacam2 genes.

Authors:  E Han; D Phan; P Lo; M N Poy; R Behringer; S M Najjar; S H Lin
Journal:  Biochem J       Date:  2001-04-15       Impact factor: 3.857

2.  Development of a novel splice array platform and its application in the identification of alternative splice variants in lung cancer.

Authors:  Ruben Pio; David Blanco; Maria Jose Pajares; Elena Aibar; Olga Durany; Teresa Ezponda; Jackeline Agorreta; Javier Gomez-Roman; Miguel Angel Anton; Angel Rubio; Maria D Lozano; Jose M López-Picazo; Francesc Subirada; Tamara Maes; Luis M Montuenga
Journal:  BMC Genomics       Date:  2010-06-03       Impact factor: 3.969

3.  CEACAM1-4S, a cell-cell adhesion molecule, mediates apoptosis and reverts mammary carcinoma cells to a normal morphogenic phenotype in a 3D culture.

Authors:  Julia Kirshner; Charng-Jui Chen; Pingfang Liu; Jie Huang; John E Shively
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-09       Impact factor: 11.205

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

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.