Document Detail


Telomerase activity and expression of human telomerase catalytic subunit gene in esophageal tissues.
MedLine Citation:
PMID:  12108675     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Telomerase, the ribonucleoprotein enzyme that synthesizes telomeric DNA, is thought to be necessary for cellular immortality and carcinogenesis. Telomerase activity is associated with the majority of malignant human cancers. The mRNA that encodes the telomerase catalytic subunit (human telomerase repeat transcriptase; hTERT) has recently been identified, and the expression of the hTERT gene is thought to regulate the activation of telomerase. However, the expression of hTERT mRNA in esophageal tissues has not been reported. We investigated hTERT gene expression in cancerous and noncancerous esophageal tissues, and determined the relationship between hTERT mRNA expression and telomerase activity. METHODS: Tissues from esophageal carcinomas in 14 patients, reflux esophagitis in 12 patients, esophageal acanthosis in 2 patients, esophageal papilloma in 1 patient, radiation esophagitis in 1 patient, and normal esophageal epithelium in 11 patients (including 3 specimens of normal epithelium from patients with esophageal carcinoma) were examined. All specimens were taken endoscopically. hTERT gene expression was investigated using reverse transcription-polymerase chain reaction (RT-PCR). Quantitative analysis of telomerase activity was analyzed by fluorescence telomeric repeat amplification protocol (F-TRAP) assay. RESULTS: Thirteen of the 14 (93%) esophageal carcinoma specimens expressed hTERT mRNA and revealed detectable telomerase activity. Noncancerous esophageal lesions had not only hTERT mRNA expression with a high frequency (14 of 16 cases; 88%) but also detectable telomerase activity (12 of 13 cases; 92%). Normal esophageal epithelium also highly expressed hTERT mRNA (10 of 11 cases; 91%) and revealed detectable telomerase activity (all 9 cases; 100%). In 32 of the 35 specimens analyzed for both hTERT mRNA and telomerase activity (91%), the expression of hTERT mRNA was consistent with detectable telomerase activity. CONCLUSIONS: The expression of hTERT mRNA was detected not only in cancerous but also in noncancerous esophageal tissues at a high frequency. This result was different from that reported for other gastrointestinal epithelium. Moreover, telomerase activity in esophageal carcinoma was significantly stronger than that in reflux esophagitis and normal epithelium. In addition, there was a strong relation ship between the detection of telomerase activity and the expression of hTERT mRNA in cancerous and noncancerous esophageal tissues. Thus, the qualitative analysis of hTERT mRNA expression may not be useful as a biomarker of carcinoma in esophageal tissues. Nevertheless, the quantitative analysis of telomerase activity may be somewhat useful.
Authors:
Tatsuro Tominaga; Hiromasa Kashimura; Kaori Suzuki; Akira Nakahara; Naomi Tanaka; Masayuki Noguchi; Masayuki Itabashi; Jun Ohkawa
Related Documents :
17230515 - Has1 expression in bladder cancer and its relation to urinary ha test.
18357395 - Aberrant expression of the glycolytic enzymes aldolase b and type ii hexokinase in hepa...
11869375 - Quantification of telomerase activity, porphobilinogen deaminase and human telomerase r...
12183435 - Molecular changes associated with oral dysplasia progression and acquisition of immorta...
24318355 - Cellular localization and developmental changes of the different isoforms of divalent m...
21303825 - Differential responses to salt supplementation in adult male and female rat adrenal gla...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of gastroenterology     Volume:  37     ISSN:  0944-1174     ISO Abbreviation:  J. Gastroenterol.     Publication Date:  2002  
Date Detail:
Created Date:  2002-07-10     Completed Date:  2003-01-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9430794     Medline TA:  J Gastroenterol     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  418-27     Citation Subset:  IM    
Affiliation:
Department of Internal Medicine, Institute of Clinical Medicine, University of Tsukuba, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Aged, 80 and over
Biological Markers / analysis*
DNA-Binding Proteins
Esophageal Diseases / enzymology*
Esophageal Neoplasms / enzymology*
Esophagitis, Peptic / enzymology
Esophagus / enzymology*
Female
Humans
Male
Middle Aged
RNA, Messenger / analysis*
Telomerase / genetics*,  metabolism*
Chemical
Reg. No./Substance:
0/Biological Markers; 0/DNA-Binding Proteins; 0/RNA, Messenger; EC 2.7.7.49/Telomerase
Comments/Corrections
Comment In:
J Gastroenterol. 2002;37(6):488-90   [PMID:  12108688 ]

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


Previous Document:  US Environmental Protection Agency Method 326.0, a new method for monitoring inorganic oxyhalides an...
Next Document:  Immunological and molecular analysis of B lymphocytes in low-grade MALT lymphoma of the stomach. Are...