Article

[Expression spectra of apoptosis-related gene pnas-2].

Department of Hematology, Renji Hospital & Shanghai Institute of Hematology, Medical College, Shanghai Jiaotong University, Shanghai 200001, China.
Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 05/2008; 16(2):282-5. pp.282-5
Source: PubMed

ABSTRACT To explore the expression spectra of apoptosis-related gene pnas-2 in normal tissues and acute leukemia (AL) patient tissues, the expressions of pnas-2 gene in tissues including heart, brain, placenta, lung, liver, skeletal muscle, kidney, pancreas, spleen, lymph node, thymus, leukocyte, bone marrow and fetal liver were detected by Northern blot. The expressions of pnas-2 in samples including 44 de novo, 9 non-CR, 27 CR and 12 relapsed AL patients were measured by real-time RT-PCR and Northern blot, and the expression levels of pnas-2 in normal and tumor tissues from 31 patients with malignancies were also detected. The results showed that pnas-2 was not expressed in the most tissues except in placenta. The results of real-time PCR indicated that pnas-2 expressions in samples of de novo, non-CR and relapsed patients ware significantly higher than that in CR, tumor tissues and normal tissues. In serial monitoring of 7 AL patients, the expression level of pnas-2 was high at first visit examination, but remarkably decreased after remission, and the pnas-2 expression level increased again when relapsed. It is concluded that the pnas-2 is specifically up-regulated in acute leukemia patients, which might be an oncogene and participate in leukemogenesis.

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Keywords

12 relapsed AL patients
 
7 AL patients
 
acute leukemia patients
 
apoptosis-related gene pnas-2
 
expression level
 
expression levels
 
expression spectra
 
fetal liver
 
normal
 
normal tissues
 
Northern blot
 
pnas-2 expression level
 
pnas-2 expressions
 
pnas-2 gene
 
real-time PCR
 
real-time RT-PCR
 
relapsed patients ware
 
serial monitoring
 
skeletal muscle
 
tumor tissues
 

Hai-Rong Wang