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Activated p38-MAPK and gemcitabine sensitivity in recurrent ovarian cancer.

AbstractBACKGROUND:
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.
AuthorsRenate Klotz, Alain Gustave Zeimet, Daniel Reimer, Elisabeth Müller-Holzner, Martina Chamson, Christian Marth
JournalAnticancer research (Anticancer Res) 2008 Sep-Oct Vol. 28 Issue 5B Pg. 2975-80 ISSN: 0250-7005 [Print] Greece
PMID19031942 (Publication Type: Journal Article)
Chemical References
  • Antimetabolites, Antineoplastic
  • Deoxycytidine
  • p38 Mitogen-Activated Protein Kinases
  • Gemcitabine
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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