PT - JOURNAL ARTICLE AU - Abou-Ghazal, Mohamed AU - Yang, David S. AU - Qiao, Wei AU - Reina-Ortiz, Chantal AU - Wei, Jun AU - Kong, Ling-Yuan AU - Fuller, Gregory N. AU - Hiraoka, Nobuyoshi AU - Priebe, Waldemar AU - Sawaya, Raymond AU - Heimberger, Amy B. TI - The Incidence, Correlation with Tumor-Infiltrating Inflammation, and Prognosis of Phosphorylated STAT3 Expression in Human Gliomas AID - 10.1158/1078-0432.CCR-08-1329 DP - 2008 Dec 15 TA - Clinical Cancer Research PG - 8228--8235 VI - 14 IP - 24 4099 - http://clincancerres.aacrjournals.org/content/14/24/8228.short 4100 - http://clincancerres.aacrjournals.org/content/14/24/8228.full SO - Clin Cancer Res2008 Dec 15; 14 AB - Purpose: The signal transducer and activator of transcription 3 (STAT3) is frequently overexpressed in most cancers, propagates tumorigenesis, and is a key regulator of immune suppression in cancer patients. We sought to determine the incidence of phosphorylated STAT3 (p-STAT3) expression in malignant gliomas of different pathologic types, whether p-STAT3 expression is a negative prognostic factor, and whether p-STAT3 expression influences the inflammatory response within gliomas. Methods: Using immunohistochemical analysis, we measured the incidence of p-STAT3 expression in 129 patients with gliomas of various pathologic types in a glioma tissue microarray. We categorized our results according to the total number of p-STAT3–expressing cells within the gliomas and correlated this number with the number of infiltrating T cells and T regulatory cells. We then evaluated the association between p-STAT3 expression and median survival time using univariate and multivariate analyses. Results: We did not detect p-STAT3 expression in normal brain tissues or low-grade astrocytomas. We observed significant differences in the incidence of p-STAT3 expression between the different grades of astrocytomas and different pathologic glioma types. p-STAT3 expression was associated with the population of tumor-infiltrating immune cells but not with that of T regulatory cells. On univariate analysis, we found that p-STAT3 expression within anaplastic astrocytomas was a negative prognostic factor. Conclusions: p-STAT3 expression is common within gliomas of both the astrocytic and oligodendroglial lineages and portends poor survival in patients with anaplastic astrocytomas. p-STAT3 expression differs significantly between gliomas of different pathologic types and grades and correlated with the degree of immune infiltration.