Abstract | BACKGROUND: Our study aimed to investigate if p38-MAPK determined in primary ovarian cancer can serve as a predictive marker for sensitivity to gemcitabine treatment in recurrent disease. MATERIALS AND METHODS: Activated (phosphorylated) p38-MAPK was immunohistochemically assessed in paraffin-embedded tumors obtained at primary debulking surgery from 45 patients treated with gemcitabine for platinum-resistant recurrence. The value of activated p38-MAPK in predicting sensitivity to gemcitabine treatment was statistically evaluated. RESULTS: Activated p38-MAPK was demonstrated in all healthy ovaries and all ovarian carcinomas examined. In controls, the median histological score (H-score) for activated p38-MAPK staining was 200, while in ovarian cancer the median H-score was 100. Activity of p38-MAPK in ovarian cancer tissue was not associated with overall response or survival after gemcitabine chemotherapy. CONCLUSION: P38-MAPK activity, determined by immunohistochemistry in ovarian cancer specimens obtained at primary diagnosis, cannot serve as a predictive marker for sensitivity to gemcitabine treatment in platinum-resistant disease.
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Authors | Renate Klotz, Alain Gustave Zeimet, Daniel Reimer, Elisabeth Müller-Holzner, Martina Chamson, Christian Marth |
Journal | Anticancer research
(Anticancer Res)
2008 Sep-Oct
Vol. 28
Issue 5B
Pg. 2975-80
ISSN: 0250-7005 [Print] Greece |
PMID | 19031942
(Publication Type: Journal Article)
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Chemical References |
- Antimetabolites, Antineoplastic
- Deoxycytidine
- p38 Mitogen-Activated Protein Kinases
- Gemcitabine
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Topics |
- Adult
- Aged
- Antimetabolites, Antineoplastic
(therapeutic use)
- Deoxycytidine
(analogs & derivatives, therapeutic use)
- Enzyme Activation
- Female
- Humans
- Immunohistochemistry
- Middle Aged
- Neoplasm Recurrence, Local
(drug therapy, enzymology, pathology)
- Neoplasm Staging
- Ovarian Neoplasms
(drug therapy, enzymology, pathology)
- Retrospective Studies
- p38 Mitogen-Activated Protein Kinases
(metabolism)
- Gemcitabine
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