Document Detail


Micronucleus analysis in patients with colorectal adenocarcinoma and colorectal polyps.
MedLine Citation:
PMID:  19058310     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
AIM: To determine, by counting micronucleus (MN) frequencies, whether chromosomal or DNA damage have an effect on the pathogenesis of early colorectal adenocarcinoma (CRC). METHODS: We analyzed MN frequencies in 21 patients with CRC, 24 patients with colon polyps [10 neoplastic polyps (NP) and 14 non-neoplastic polyps (NNP)] and 20 normal controls. RESULTS: MN frequency was significantly increased in CRC patients and in NP patients compared with controls (3.72 +/- 1.34, 3.58 +/- 1.21 vs 1.97 +/- 0.81, P < 0.001). However, there was no difference in the MN frequency between CRC patients and NP patients (P > 0.05). Similarly, there was no difference in the MN frequency between NNP patients (2.06 +/- 0.85) and controls (P > 0.05). CONCLUSION: Our results suggest increased chromosome/DNA instabilities may be associated with the pathogenesis of early CRC.
Authors:
Ali Karaman; Doğan Nasir Binici; Mehmet Eşref Kabalar; Züleyha Calikuşu
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  World journal of gastroenterology : WJG     Volume:  14     ISSN:  1007-9327     ISO Abbreviation:  World J. Gastroenterol.     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-12-05     Completed Date:  2009-04-09     Revised Date:  2010-09-23    
Medline Journal Info:
Nlm Unique ID:  100883448     Medline TA:  World J Gastroenterol     Country:  China    
Other Details:
Languages:  eng     Pagination:  6835-9     Citation Subset:  IM    
Affiliation:
Erzurum Training and Research Hospital, Department of Medical Genetics, Erzurum 25240, Turkey. alikaramandr@hotmail.com
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MeSH Terms
Descriptor/Qualifier:
Adenocarcinoma / genetics*,  pathology
Aged
Case-Control Studies
Cell Transformation, Neoplastic / genetics
Cells, Cultured
Colonic Polyps / genetics*,  pathology
Colonoscopy
Colorectal Neoplasms / genetics*,  pathology
Female
Gene Expression Regulation, Neoplastic
Genomic Instability*
Humans
Male
Micronuclei, Chromosome-Defective*
Micronucleus Tests
Middle Aged
Precancerous Conditions / genetics*,  pathology
Comments/Corrections

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


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