Literature DB >> 25762479

Clinical and biological significance of glucocorticoid receptor (GR) expression in breast cancer.

Rezvan Abduljabbar1, Ola H Negm, Chun-Fui Lai, Dena A Jerjees, Methaq Al-Kaabi, Mohamed R Hamed, Patrick J Tighe, Lakjaya Buluwela, Abhik Mukherjee, Andrew R Green, Simak Ali, Emad A Rakha, Ian O Ellis.   

Abstract

The glucocorticoid receptor (GR) is a member of the nuclear receptor superfamily of transcription factors, which exerts anti-proliferative and anti-apoptotic activities. The GR is expressed in a large proportion of breast cancer (BC) although levels generally decrease during cancer progression. This study aimed to determine the clinical and biological significance of GR expression using a large series of early-stage BC with long-term follow-up and BC cell lines. Immunohistochemistry was used to assess the expression of GR in 999 cases of primary invasive BC prepared as tissue microarrays. Reverse phase protein microarray was used to assess the expression of GR in MCF7 and MDA-MB-231 cell lines. Nuclear expression of GR was observed in 61.6 % of breast tumours and was associated with features of good prognosis including smaller tumour size and lower grade with less pleomorphism and low mitotic count. GR expression was positively correlated with expression of oestrogen (ER) and progesterone receptors. In ER-positive tumours, GR was associated with other features of favourable outcome including FOXA1, GATA3 and BEX1 expression, while low GR expression was associated with high Ki67, p53 and CD71 expression. GR expression is associated with features of good outcome but does not provide prognostic information independent of size, stage and grade. Understanding the receptor and its effects on BC behaviour is essential for avoiding any unwanted effects from the use of glucocorticoids in routine oncology practice.

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Year:  2015        PMID: 25762479     DOI: 10.1007/s10549-015-3335-1

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  33 in total

1.  Association of lifestyle and demographic factors with estrogenic and glucocorticogenic activity in Mexican American women.

Authors:  L Fejerman; S S Sanchez; R Thomas; P Tachachartvanich; J Riby; S L Gomez; E M John; M T Smith
Journal:  Carcinogenesis       Date:  2016-07-13       Impact factor: 4.944

Review 2.  Steroid Hormone Receptor Positive Breast Cancer Patient-Derived Xenografts.

Authors:  Shawna B Matthews; Carol A Sartorius
Journal:  Horm Cancer       Date:  2016-10-28       Impact factor: 3.869

Review 3.  Schwann cells: a new player in the tumor microenvironment.

Authors:  Yuri L Bunimovich; Anton A Keskinov; Galina V Shurin; Michael R Shurin
Journal:  Cancer Immunol Immunother       Date:  2016-11-24       Impact factor: 6.968

4.  Glucocorticoid receptor antagonism overcomes resistance to BRAF inhibition in BRAFV600E-mutated metastatic melanoma.

Authors:  José M Estrela; Rosario Salvador; Patricia Marchio; Soraya L Valles; Rafael López-Blanch; Pilar Rivera; María Benlloch; Javier Alcácer; Carlos L Pérez; José A Pellicer; Elena Obrador
Journal:  Am J Cancer Res       Date:  2019-12-01       Impact factor: 6.166

5.  Hsp90 Inhibition Results in Glucocorticoid Receptor Degradation in Association with Increased Sensitivity to Paclitaxel in Triple-Negative Breast Cancer.

Authors:  Abena S Agyeman; Wesley J Jun; David A Proia; Caroline R Kim; Maxwell N Skor; Masha Kocherginsky; Suzanne D Conzen
Journal:  Horm Cancer       Date:  2016-02-08       Impact factor: 3.869

6.  Glucocorticoid receptor activation inhibits chemotherapy-induced cell death in high-grade serous ovarian carcinoma.

Authors:  Erica M Stringer-Reasor; Gabrielle M Baker; Maxwell N Skor; Masha Kocherginsky; Ernst Lengyel; Gini F Fleming; Suzanne D Conzen
Journal:  Gynecol Oncol       Date:  2015-06-24       Impact factor: 5.482

7.  GR and ER Coactivation Alters the Expression of Differentiation Genes and Associates with Improved ER+ Breast Cancer Outcome.

Authors:  Diana C West; Deng Pan; Eva Y Tonsing-Carter; Kyle M Hernandez; Charles F Pierce; Sarah C Styke; Kathleen R Bowie; Tzintzuni I Garcia; Masha Kocherginsky; Suzanne D Conzen
Journal:  Mol Cancer Res       Date:  2016-05-02       Impact factor: 5.852

8.  Discovery of a Glucocorticoid Receptor (GR) Activity Signature Using Selective GR Antagonism in ER-Negative Breast Cancer.

Authors:  Diana C West; Masha Kocherginsky; Eva Y Tonsing-Carter; D Nesli Dolcen; David J Hosfield; Ricardo R Lastra; Jason P Sinnwell; Kevin J Thompson; Kathleen R Bowie; Ryan V Harkless; Maxwell N Skor; Charles F Pierce; Sarah C Styke; Caroline R Kim; Larischa de Wet; Geoffrey L Greene; Judy C Boughey; Matthew P Goetz; Krishna R Kalari; Liewei Wang; Gini F Fleming; Balázs Györffy; Suzanne D Conzen
Journal:  Clin Cancer Res       Date:  2018-04-10       Impact factor: 12.531

9.  Glucocorticoid Receptor:MegaTrans Switching Mediates the Repression of an ERα-Regulated Transcriptional Program.

Authors:  Feng Yang; Qi Ma; Zhijie Liu; Wenbo Li; Yuliang Tan; Chunyu Jin; Wubin Ma; Yiren Hu; Jia Shen; Kenneth A Ohgi; Francesca Telese; Wen Liu; Michael G Rosenfeld
Journal:  Mol Cell       Date:  2017-05-04       Impact factor: 17.970

10.  Expression of CDK7, Cyclin H, and MAT1 Is Elevated in Breast Cancer and Is Prognostic in Estrogen Receptor-Positive Breast Cancer.

Authors:  Hetal Patel; Rezvan Abduljabbar; Chun-Fui Lai; Manikandan Periyasamy; Alison Harrod; Carolina Gemma; Jennifer H Steel; Naina Patel; Claudia Busonero; Dena Jerjees; Judit Remenyi; Sally Smith; Jennifer J Gomm; Luca Magnani; Balázs Győrffy; Louise J Jones; Frances Fuller-Pace; Sami Shousha; Laki Buluwela; Emad A Rakha; Ian O Ellis; R Charles Coombes; Simak Ali
Journal:  Clin Cancer Res       Date:  2016-06-14       Impact factor: 12.531

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