The number of regulatory T cells in prostate cancer is associated with the androgen receptor and hypoxia-inducible factor (HIF)-2α but not HIF-1α

被引:24
|
作者
Fox, Stephen B.
Launchbury, Rosalind
Bates, Gaynor J.
Han, Cheng
Shaida, Nadeem
Malone, Peter R.
Harris, Adrian L.
Banham, Alison H.
机构
[1] Peter MacCallum Canc Ctr, Dept Pathol, Melbourne, Vic 3002, Australia
[2] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, LRF Lymphoma Antigens Grp, Oxford OX3 9DU, England
[3] Royal Berkshire Hosp, Harold Hopkins Dept Urol, Reading RG1 5AN, Berks, England
[4] Univ Oxford, Weatherall Inst Mol Med, Canc Res UK Mol Oncol Lab, Oxford OX1 2JD, England
来源
PROSTATE | 2007年 / 67卷 / 06期
关键词
FOXP3; forkhead; regulatory T-cell; prognosis; prostate cancer;
D O I
10.1002/pros.20538
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Regulatory T cells (T-R) mediate peripheral immunological tolerance and are implicated in tumor progression. Because prostate cancer is being investigated for treatment by immunotherapy, we have assessed tumor TR in prostate cancers. METHODS. TR cells were identified by FOXP3 in tissue microarrays (TMAs) from 146 radical prostatectomies and correlated with clinicopathological tumor parameters and prostatic specific antigen rise (PSA). RESULTS. Twenty of 146 tumors contained no TR. The mean of the average for the remaining 146 patients was 7.24. There was a significant correlation between TR and androgen receptor (P = 0.003) and with hypoxia-inducible factor (HIF)-2 alpha (P = 0.007) but not HIF-1 alpha (P = 0.25). There was no significant correlation between TR numbers and stage, capsular invasion, urethral margins, vascular invasion, Gleason score, pre-operative PSA, or time to PSA recurrence (all P > 0.05). CONCLUSIONS. TR in prostate tumors shows significant heterogeneity and maybe the result of hormonal and hypoxic signaling. Targeting these may reduce TR in tumors allowing more successful immune therapies.
引用
收藏
页码:623 / 629
页数:7
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