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[hTERT gene expression in children with beta-thalassemia major].

作者信息

Li Xi-Hong, Tang Jun, Guo Wen-Jun, Qu Yi, Yu Fan, Wang Xiao-Yang, Wang Feng-Lan, Mu De-Zhi

机构信息

Department of Pediatrics, West China Second Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Jun;11(6):449-52.

PMID:19558808
Abstract

OBJECTIVE

Human telomerase reverse transcriptase (hTERT) is a rate-limiting enzyme which dictates the activity of human telomerase and thus decides the life span of cells. The aim of this study was to explore the expression of hTERT in bone marrow from children with beta-thalassemia major and the relationship between the expression of hTERT and hemoglobin levels.

METHODS

Multiple allele specific polymerase chain reaction (MASPCR) was used for targeted DNA amplification and gene mutation analysis of beta-thalassemia. hTERT mRNA expression in bone marrow was examined using real-time reverse transcription polymerase chain reaction (RT-PCR) analysis in 29 children with beta-thalassemia major, in 10 children with agranulocytosis and in K562 cell line. The hemoglobin levels in peripheral blood were measured. The relationship between hTERT expression and hemoglobin levels was evaluated by the Spearman test in the beta-thalassemia major group.

RESULTS

hTERT mRNA expression significantly increased in bone marrow from children with beta-thalassemia major compared with that from children with agranulocytosis (0.2928+/- 0.0838 vs 0.0993+/- 0.0336; P<0.01), but was significantly lower than that in K562 cell line (0.8291+/- 0.0908) (P<0.01). A significantly inverse correlation was found between hTERT mRNA expression and hemoglobin levels (r=-0.841, P<0.01).

CONCLUSIONS

A low hemoglobin concentration might contribute to the up-regulation of marrow hTERT expression in children with beta-thalassemia major.

摘要

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