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Prognostic investigations of B7-H1 and B7-H4 expression levels as independent predictor markers of renal cell carcinoma.

Authors :
Safaei, Hamid
Rostamzadeh, Ayoob
Rahmani, Omid
Mohammadi, Mohsen
Ghaderi, Omar
Yahaghi, Hamid
Ahmadi, Koroosh
Source :
Tumor Biology (Springer Science & Business Media B.V.); Jun2016, Vol. 37 Issue 6, p7583-7587, 5p
Publication Year :
2016

Abstract

In order to evaluate the correlation of B7-H4 and B7-H1 with renal cell carcinoma (RCC), we analyzed B7-H1 and B7-H4 expressions and their clinical significance by immunohistochemical method. Our result indicated that B7-H4-positive staining was detected in 58.13 % of RCC tissues (25 tissues tumors), and there were 18 tissues of patients without detectable B7-H4. Furthermore, 21 cases (48.83 %) were B7-H1-positive. Positive tumor expressions of B7-H4 and B7-H1 were markedly related to advanced TNM stage ( P = 0.001; P = 0.014), high grade ( P = 0.001; P = 002), and larger tumor size ( P = 0.002; P = 024) in RCC tissues than patients with B7-H4-negative and B7-H1-negative in RCC tissues. The patients with B7-H1 and B7-H4-positive expressions were found to be markedly correlated with the overall survival of the patients ( P < 0.05) and tended to have an increased risk of death when compared with negative expression groups. Univariate analysis showed that B7-H4 and B7-H1 expressions, TNM stage, high grade, and tumor size were significantly related to the prognosis of RCC. Furthermore, multivariate analysis showed that B7-H4 and B7-H1 expressions decreased overall survival. The adjusted HR for B7-H1 was 2.83 (95 % CI 1.210-2.971; P = 0.031) and also was 2.918 (95 % CI 1.243-3.102; P = 0.006) for B7-H4 that showed these markers were independent prognostic factors in RCC patients. The expressions of B7-H1 and B7-H4 in RCC patients indicate that these markers may be as a predictor of tumor development and death risk. Further investigations can be helpful to confirm B7-H1 and B7-H4 roles as an independent predictor of clinical RCC outcome. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10104283
Volume :
37
Issue :
6
Database :
Complementary Index
Journal :
Tumor Biology (Springer Science & Business Media B.V.)
Publication Type :
Academic Journal
Accession number :
115528734
Full Text :
https://doi.org/10.1007/s13277-015-4652-z