Favorable prognostic influence of T-box transcription factor Eomesodermin in metastatic renal cell cancer patients

被引:14
作者
Dielmann, Anastasia [1 ]
Letsch, Anne [1 ]
Nonnenmacher, Anika [1 ]
Miller, Kurt [2 ]
Keilholz, Ulrich [1 ]
Busse, Antonia [1 ]
机构
[1] Charite, Dept Med Hematol Oncol & Tumor Immunol 3, Campus Benjamin Franklin, Hindenburgdamm 30, D-12200 Berlin, Germany
[2] Charite, Dept Urol, Campus Benjamin Franklin, D-13353 Berlin, Germany
关键词
Renal cell carcinoma; Memory T cells; Effector T cells; T-box expressed in T cells; Eomesodermin; Natural killer cells; ENDOTHELIAL GROWTH-FACTOR; GLOBAL EVALUATION TRIAL; C-REACTIVE PROTEIN; COLORECTAL-CANCER; TUMOR BIOLOGY; IMMUNE CELLS; IFN-GAMMA; TGF-BETA; CARCINOMA; EXPRESSION;
D O I
10.1007/s00262-015-1786-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
T-box transcription factors, T-box expressed in T cells (T-bet) encoded by Tbx21 and Eomesodermin (Eomes), drive the differentiation of effector/memory T cell lineages and NK cells. The aim of the study was to determine the prognostic influence of the expression of these transcription factors in peripheral blood (pB) in a cohort of 41 metastatic (m) RCC patients before receiving sorafenib treatment and to analyze their association with the immunophenotype in pB. In contrast to Tbx21, in the multivariate analysis including clinical features, Eomes mRNA expression was identified as an independent good prognostic factor for progression-free survival (PFS, p = 0.042) and overall survival (OS, p = 0.001) in addition to a favorable ECOG performance status (p = 0.01 and p = 0.008, respectively). Eomes expression correlated positively not only with expression of Tbx21 and TGF beta 1 mRNA, but also with mRNA expression of the activation marker ICOS, and with in vivo activated HLA-DR+ T cells. Eomes expression was negatively associated with TNF alpha-producing T cells. On protein level, Eomes was mainly expressed by CD56(+)CD3(-) NK cells in pB. In conclusion, we identified a higher Eomes mRNA expression as an independent good prognostic factor for OS and PFS in mRCC patients treated with sorafenib.
引用
收藏
页码:181 / 192
页数:12
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