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High level expression of glucocorticoid receptor (GR) is linked to aggressive tumor features, early biochemical recurrence, and genetic instability in prostate cancer.


ABSTRACT:

Background

The glucocorticoid receptor (GR) is a nuclear receptor protein for cortisol and other glucocorticoids and regulates the transcription of thousands of genes involved in metabolism, development, stress and inflammatory response. In prostate cancer, GR may confer resistance to anti-androgen receptor therapies by bypassing AR blockade. However, only few data are available on the prognostic role of GR expression in prostate cancer.

Methods

To estimate the prognostic value of GR, a tissue microarray containing 17,747 prostate cancers with associated follow-up and molecular data was analyzed by immunohistochemistry.

Results

All patients had undergone radical prostatectomy. GR immunostaining was found in 10,832 (89.1%) of 12,125 interpretable tumors, including 48.5% with weak, 29.8% with moderate and 11% with strong staining intensity. Increased GR staining was strongly linked to adverse feature of the disease, including high tumor stage (pT), high classical and quantitative Gleason grade, presence of nodal metastases (pN+), a positive surgical margin (R1) status, and early biochemical recurrence (p < 0.0001 each). A multivariate analysis showed that the prognostic value of strong GR staining was independent of pT, Gleason grade, pN and R status. High level GR staining was significantly linked to TMPRSS2:ERG fusion (p < 0.0001) and high androgen receptor expression (p < 0.0001 each). A combined analysis of the impact of GR and AR on patient prognosis identified the best prognosis for ARneg/GRneg cancers while ARpos/GRpos cancers showed the worst prognosis (p < 0.0001). Moreover, high GR expression was a strong predictor of poor prognosis in AR low, AR intermediate and AR high cancers (p < 0.0001 each).

Conclusion

High level expression of GR is strongly linked to prostate cancer aggressiveness in uni- and multivariate analysis. GR immunohistochemistry - alone or in combination with other markers - holds great potential to identify patients with a high risk for tumor progression.

SUBMITTER: Heckmann N 

PROVIDER: S-EPMC12909130 | biostudies-literature | 2026 Mar

REPOSITORIES: biostudies-literature

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High level expression of glucocorticoid receptor (GR) is linked to aggressive tumor features, early biochemical recurrence, and genetic instability in prostate cancer.

Heckmann Neele N   Plage Henning H   Simon Ronald R   Lennartz Maximilian M   Fraune Christoph C   Jacobsen Frank F   Krech Till T   Lebok Patrick P   Minner Sarah S   Burandt Eike E   Clauditz Till S TS   Wilczak Waldemar W   Sauter Guido G   Gorbokon Natalia N   Freytag Morton M   Lutz Florian F   Reiswich Viktor V   Viehweger Florian F   Chirico Viktoria V   Heinzer Hans H   Haese Alexander A   Schlomm Thorsten T   Marx Andreas A   Graefen Markus M   Steurer Stefan S   Bernreuther Christian C   Ralla Bernhard B   Dum David D   Hinsch Andrea A   Kind Simon S   Luebke Andreas M AM   Menz Anne A   Möller Katharina K   Schlichter Ria R   Weidemann Sören S   Erber Barbara B   Biernath Nadine N   Weinberger Sarah S  

Prostate cancer and prostatic diseases 20251105 1


<h4>Background</h4>The glucocorticoid receptor (GR) is a nuclear receptor protein for cortisol and other glucocorticoids and regulates the transcription of thousands of genes involved in metabolism, development, stress and inflammatory response. In prostate cancer, GR may confer resistance to anti-androgen receptor therapies by bypassing AR blockade. However, only few data are available on the prognostic role of GR expression in prostate cancer.<h4>Methods</h4>To estimate the prognostic value of  ...[more]

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