Document Detail


Bronchogenic and alveologenic tumors in mice induced by N-nitrosopiperidine.
MedLine Citation:
PMID:  20651851     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The aim of this study was to explore the histogenesis and carcinogenesis of pulmonary cancer induced by N-nitrosopiperidine (NPIP) in mice. NPIP is a form of N-nitrosamine found in tobacco smoke, which has been shown to be a genotoxic chemical as well as a mutagenic compound for inducing chromosome aberrations and severe clastogenicity. In this study, 80 BALB/C strain mice were injected with 0.2 mmol/kg NPIP intraperitoneally for 8 weeks, and experiments were conducted for a further 16 weeks. For the control group, 40 mice were injected with an equal volume of 0.9% NaCl. Pulmonary tissues and tumors in the NPIP-treated group were examined by light microscopy and transmission electron microscopy and compared with the control group at 4-week intervals. The mRNA levels of p53 (mutant), bcl-2, c-myc, ras, and subunits of telomerase - telomerase reverse transcriptase (TERT) and an RNA component, TR - were assayed by mPCR or RT-PCR. Twenty-two mice in the experimental group were found to develop pulmonary tumors, but none in the control group. All tumors found in the experimental group originated from alveolar type II epithelial cells. In addition, 6 of the 22 mice also developed tumors of bronchogenic origin. The expression of p53, bcl-2, c-myc, ras, and the subunits of telomerase were found to increase in all pulmonary tissues and tumors formed thereafter upon NPIP treatment. In summary, NPIP-induced mouse lung tumors exhibited morphological changes during carcinogenesis, which may be the consequence of overexpression of some genes associated with the development of carcinoma and changes in subunits of telomerase. This mouse model of lung tumor formation may be a useful tool to delineate the histogenesis and carcinogenesis of human pulmonary cancer.
Authors:
Xiao-Yuan Xie; Jian Shen; Li-Yan Xu; En-Min Li; Zhong-Ying Shen
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Biochemistry and cell biology = Biochimie et biologie cellulaire     Volume:  88     ISSN:  1208-6002     ISO Abbreviation:  Biochem. Cell Biol.     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-07-23     Completed Date:  2010-12-15     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8606068     Medline TA:  Biochem Cell Biol     Country:  Canada    
Other Details:
Languages:  eng     Pagination:  775-82     Citation Subset:  IM    
Affiliation:
Department of Tumor Medicine, The First Affiliated Hospital, Shantou University Medical College, Shantou, P.R. China. starsea65@163.com
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenoma / chemically induced,  genetics,  pathology,  ultrastructure
Animals
Carcinoma, Bronchogenic / chemically induced*,  genetics,  pathology,  ultrastructure
Carcinoma, Squamous Cell / chemically induced,  genetics,  pathology,  ultrastructure
Female
Gene Expression Regulation, Neoplastic
Genes, bcl-2
Genes, myc
Genes, p53
Genes, ras
Lung Neoplasms / chemically induced*,  genetics,  pathology,  ultrastructure
Male
Mice
Mice, Inbred BALB C
Nitrosamines*
Pulmonary Alveoli / drug effects,  metabolism,  pathology,  ultrastructure
Telomerase / genetics,  metabolism
Chemical
Reg. No./Substance:
0/Nitrosamines; 100-75-4/N-nitrosopiperidine; EC 2.7.7.49/Telomerase; EC 2.7.7.49/Tert protein, mouse

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


Previous Document:  Apoptosis induced by emodin is associated with alterations of intracellular acidification and reacti...
Next Document:  Impact of growth environment and physiological state on metal immobilization by Pseudomonas aerugino...