Journal
CANCER BIOLOGY & THERAPY
Volume 7, Issue 3, Pages 340-344Publisher
TAYLOR & FRANCIS INC
DOI: 10.4161/cbt.7.3.5422
Keywords
autoantibody; biomarker; nasopharyngeal carcinoma; BMI-1; early diagnosis
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BMI-1 is overexpressed in a variety of cancers, which can activate the immune system to produce antibodies in tumor tissues. In this study, we isolated phage expressing BMI-1 protein by screening of a mixture of nasopharyngeal carcinoma ( NPC) cDNA T7 phage library and found that the antibody against BMI-1 was elevated in the sera from NPC patients. BMI-1 mRNA was overexpressed at different levels in seven NPC cell lines compared with normal nasopharyngeal epithelial cell line NP69. Histochemistry showed that patient sera were more reactive with BMI-1 than normal sera. Antibody affinity assay using sera from 40 NPC patients and 54 controls showed that BMI-1 antibody was significantly greater in patient sera than in normal controls ( patient 0.791 +/- 0.025 and normal 0.488 +/- 0.042; p < 0.001) and the BMI-1 autoantibody be significantly related with the progress of NPC ( Benign versus LNPC P = 0.001; LNPC versus MNPC p = 0.047). Analysis of the results with logistic regression and receiver operating characteristics ( ROC) curves showed that BMI-1 antibody was a modest marker for NPC ( sensitivity 0.74 and specificity 0.73; AUC = 0.8044). The showed that BMI-1 antibody as a potential marker of NPC may be rational, and could have diagnostic and prognostic value.
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