Molecular Diagnostics

British Journal of Cancer (2005) 92, 113–119. doi:10.1038/sj.bjc.6602244 www.bjcancer.com
Published online 7 December 2004

Enhanced expression of peroxisome proliferator-activated receptor gamma in epithelial ovarian carcinoma

G Y Zhang1, N Ahmed2,3, C Riley2, K Oliva2,3, G Barker2, M A Quinn2,3 and G E Rice2,3

  1. 1Department of Obstetrics and Gynaecology, Qilu Hospital of Shandong University, 107 Wenhuaxi Road, Jinan 250012, PR China
  2. 2Gynaecological Cancer Research Centre, The Royal Women's Hospital, 132 Grattan Street, Carlton, Victoria 3053, Australia
  3. 3Department of Obstetrics and Gynaecology, The University of Melbourne, Victoria, Australia

Correspondence: Dr N Ahmed, Gynaecological Cancer Research Centre, The Royal Women's Hospital, 132 Grattan Street, Carlton, Victoria 3053, Australia. E-mail: nuzhata@unimelb.edu.au

Received 20 June 2004; Revised 20 September 2004; Accepted 28 September 2004; Published online 7 December 2004.

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Abstract

The peroxisome proliferator-activated receptors (PPARs) belong to a subclass of nuclear hormone receptor that executes important cellular transcriptional functions. Previous studies have demonstrated the expression of PPARitalic gamma in several tumours including colon, breast, bladder, prostate, lung and stomach. This study demonstrates the relative expression of PPARitalic gamma in normal ovaries and different pathological grades of ovarian tumours of serous, mucinous, endometrioid, clear cell and mixed subtypes. A total of 56 ovarian specimens including 10 normal, eight benign, 10 borderline, seven grade 1, nine grade 2 and 12 grade 3 were analysed using immunohistochemistry. Immunoreactive PPARitalic gamma was not expressed in normal ovaries. Out of eight benign and 10 borderline tumours, only one tumour in each group showed weak cytoplasmic PPARitalic gamma expression. In contrast, 26 out of 28 carcinomas studied were positive for PPARitalic gamma expression with staining confined to cytoplasmic and nuclear regions. An altered staining pattern of PPARitalic gamma was observed in high-grade ovarian tumours with PPARitalic gamma being mostly localized in the nuclei with little cytoplasmic immunoreactivity. On the other hand, predominant cytoplasmic staining was observed in lower-grade tumours. Significantly increased PPARitalic gamma immunoreactivity was observed in malignant ovarian tumours (grade 1, 2 and 3) compared to benign and borderline tumours (chi2=48.80, P<0.001). Western blot analyses showed significant elevation in the expression of immunoreactive PPARitalic gamma in grade 3 ovarian tumours compared with that of normal ovaries and benign ovarian tumours (P<0.01). These findings suggest an involvement of PPARitalic gamma in the onset and development of ovarian carcinoma and provide an insight into the regulation of this molecule in the progression of the disease.

Keywords:

peroxisome proliferator-activated receptor, ovarian cancer, immunohistochemistry, nuclear and cytoplasmic staining