Peroxiredoxin-I is an autoimmunogenic tumor antigen in non-small cell lung cancer

被引:76
作者
Chang, JW
Lee, SH
Jeong, JY
Chae, HZ
Kim, YC
Park, ZY
Yoo, YJ [1 ]
机构
[1] GIST, Dept Life Sci, Kwangju 500712, South Korea
[2] Chonnam Natl Univ, Dept Biol, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Sch Med, Dept Internal Med, Kwangju 501757, South Korea
关键词
autoantibody; non-small cell lung cancer; peroxiredoxin-I; tumor antigen;
D O I
10.1016/j.febslet.2005.04.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In eukaryotic cells, peroxiredoxins are both antioxidants and regulators of H2O2-mediated signaling. We previously found that peroxiredoxin-I (Prx-I) was overexpressed in non-small cell lung cancer (NSCLC) tissue. Since overexpressed protein can induce a humoral immune response, we examined whether serum from NSCLC patients exhibited immunoreactivity against Prx-I using Western blotting. We found that 25 (47%) of 53 NSCLC patients tested had autoantibodies against Prx-I in their sera, whereas such activity was detected in 4 (8%) sera from 50 healthy subjects. Prx-I itself was detected in the sera from 18 (34%) of 53 NSCLC patients but in only 1 (2%) serum from 50 controls. Moreover, 17% of NSCLC sera were positive to both Prx-I antibody and antigen but none in control sera. The data indicate both Prx-I autoantibody and circulating antigen are potential biomarkers for use in serological diagnosis of NSCLC. Interestingly enough, we found that Prx-I was secreted by lung adenocarcinoma cells (A549) but not by non-cancer lung cells (BEAS 2B) or breast cancer cells (MCF7). This cell culture study suggests the possibility of Prx-I secretion from NSCLC tumor tissues. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2873 / 2877
页数:5
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