Document Detail


Analysis of p16 and p21(Cip1) expression in tumorigenic human bronchial epithelial cells induced by asbestos.
MedLine Citation:
PMID:  11704859     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Although asbestos is carcinogenic to humans, the mechanism(s) by which it induces cancer is unknown. Using tumor cell lines generated previously by asbestos treatment of immortalized human bronchial epithelial (BEP2D) cells, we examined alterations in p16 and p21(Cip1) genes together with their protein levels. Results were compared with untreated BEP2D cells, normal human bronchial epithelial cells (NHBE), as well as non-tumorigenic fusion cell lines generated by fusing tumor cells with BEP2D cells. No deletion in the p16 gene was found in any of the tumor cell lines examined. Although p16 protein was expressed at a similar level in tumor and BEP2D cells, there was a fourfold decrease in its expression among NHBE cells. In contrast, both the protein and mRNA expression levels of p21(Cip1) were decreased by about threefold in tumor cell lines when compared with either BEP2D or NHBE cells, which had a similar expression level. Expression of p21(Cip1) mRNA was restored to the control level in all the fusion cell lines examined. The results suggested that down regulation of p21(Cip1) expression is linked to the tumorigenic conversion of BEP2D cells by asbestos.
Authors:
C Q Piao; Y L Zhao; T K Hei
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Oncogene     Volume:  20     ISSN:  0950-9232     ISO Abbreviation:  Oncogene     Publication Date:  2001 Nov 
Date Detail:
Created Date:  2001-11-12     Completed Date:  2001-12-13     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8711562     Medline TA:  Oncogene     Country:  England    
Other Details:
Languages:  eng     Pagination:  7301-6     Citation Subset:  IM    
Affiliation:
Center for Radiological Research, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. cp16@columbia.edu
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MeSH Terms
Descriptor/Qualifier:
Asbestos / adverse effects*
Asbestos, Serpentine / toxicity
Bronchi / pathology*
Carcinogens / adverse effects*
Cell Line, Transformed / metabolism,  transplantation
Cell Transformation, Neoplastic / genetics
Cells, Cultured / drug effects,  metabolism
Culture Media, Serum-Free
Cyclin-Dependent Kinase Inhibitor p16 / biosynthesis*
Cyclin-Dependent Kinase Inhibitor p21
Cyclins / biosynthesis*,  genetics
Epithelial Cells / drug effects,  metabolism
Genes, p16*
Humans
Hybrid Cells / metabolism
Neoplasm Proteins / biosynthesis,  genetics
Neoplasm Transplantation
Neoplasms, Experimental / etiology
Polymerase Chain Reaction
RNA, Messenger / biosynthesis,  genetics
RNA, Neoplasm / biosynthesis,  genetics
Sequence Deletion
Tumor Cells, Cultured / metabolism,  transplantation
Grant Support
ID/Acronym/Agency:
ES05786/ES/NIEHS NIH HHS; ES07890/ES/NIEHS NIH HHS
Chemical
Reg. No./Substance:
0/Asbestos, Serpentine; 0/CDKN1A protein, human; 0/Carcinogens; 0/Culture Media, Serum-Free; 0/Cyclin-Dependent Kinase Inhibitor p16; 0/Cyclin-Dependent Kinase Inhibitor p21; 0/Cyclins; 0/Neoplasm Proteins; 0/RNA, Messenger; 0/RNA, Neoplasm; 1332-21-4/Asbestos

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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