Document Detail


Overexpression of cyclin D2 is associated with increased in vivo invasiveness of human squamous carcinoma cells.
MedLine Citation:
PMID:  12112307     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Overexpression of cyclin D2 was studied in 10 human squamous cell carcinoma lines, to establish whether this gene plays a role in tumor progression. We found that those cell lines that overexpressed cyclin D2 (CCND2) had the most invasive in vivo behavior. The invasive ability of the cell lines was determined by evaluating the penetration of carcinoma cells into the tracheal wall in an in vivo assay with de-epithelialized tracheas transplanted into the subcutaneous tissue of nude mice. From five cell lines that exhibited low invasive ability, we selected two that had very little CCND2 expression (SCC9 and SCC15), to evaluate whether CCND2 gene transfer would increase the invasive behavior. After confirming the successful transfer of CCND2 by Northern, Western, and kinase-activity assays, we assessed the in vivo invasive behavior of the CCND2-transfected cells and their respective vector alone-transfected controls. The cell lines containing the transferred CCND2 gene had a significantly higher invasive ability than respective controls. This was accompanied by a moderate increase in gelatinase activity. In addition, the in vitro proliferative abilities, under normal culture conditions, of the parental CCND2-transfected and vector alone-transfected cells were found to be similar, as was the in vivo labeling index of Ki-67 in the tracheal transplants. These results indicated that the overexpression of CCND2 in squamous cell carcinoma lines modulates cell proliferation after induced quiescence and also has a powerful enhancing effect on in vivo aggressive growth behavior.
Authors:
Shao Chen Liu; Daniel E Bassi; Shi Yu Zhang; Dana Holoran; Claudio J Conti; Andres J P Klein-Szanto
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Molecular carcinogenesis     Volume:  34     ISSN:  0899-1987     ISO Abbreviation:  Mol. Carcinog.     Publication Date:  2002 Jul 
Date Detail:
Created Date:  2002-07-11     Completed Date:  2002-09-24     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  8811105     Medline TA:  Mol Carcinog     Country:  United States    
Other Details:
Languages:  eng     Pagination:  131-9     Citation Subset:  IM    
Copyright Information:
Copyright 2002 Wiley-Liss, Inc.
Affiliation:
Department of Pathology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, 19111, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Carcinogenicity Tests / methods
Carcinoma, Squamous Cell / metabolism*,  pathology*
Cyclin D2
Cyclins / genetics,  metabolism*
Head and Neck Neoplasms / metabolism,  pathology
Humans
Mice
Mice, SCID
Neoplasm Invasiveness
Rats
Transplantation, Heterologous
Tumor Cells, Cultured
Grant Support
ID/Acronym/Agency:
CA 06927/CA/NCI NIH HHS; CA 71539/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/CCND2 protein, human; 0/Ccnd2 protein, mouse; 0/Ccnd2 protein, rat; 0/Cyclin D2; 0/Cyclins

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