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Tissue microarray analysis of hormonal signaling pathways in uterine carcinosarcoma.

AbstractOBJECTIVES: STUDY DESIGN:
Immunohistochemistry was performed on tissue arrays using standard methodology. Differences between groups were evaluated by the Wilcoxon rank-sum test. Interactions between tumor stage and receptor expression were determined by linear trend analysis.
RESULTS:
Compared with normal endometrium, carcinosarcomas exhibited low estrogen receptor alpha and progesterone receptor expression (all P < .01), but overexpressed estrogen receptor beta (P = .02). Estrogen receptor beta expression increased in advanced stage disease (P = .02). Insulin-like growth factor receptor expression was lower in carcinosarcoma compared with normal endometrium (P = .01). Human epidermal growth factor receptor 2 expression was elevated and increased with disease progression (P < .01).
CONCLUSION:
In uterine carcinosarcoma, estrogen receptor beta expression is elevated and increases with disease progression, whereas estrogen receptor alpha and progesterone receptor are suppressed. Human epidermal growth factor receptor 2 expression is increased, whereas insulin-like growth factor receptor is lower than in normal endometrium. These data support a potential role for estrogen receptor beta in disease progression via crosstalk with human epidermal growth factor receptor 2.
AuthorsGloria S Huang, Rebecca C Arend, Maomi Li, Marc J Gunter, Lydia G Chiu, Susan Band Horwitz, Gary L Goldberg
JournalAmerican journal of obstetrics and gynecology (Am J Obstet Gynecol) Vol. 200 Issue 4 Pg. 457.e1-5 (Apr 2009) ISSN: 1097-6868 [Electronic] United States
PMID19200930 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Receptors, Growth Factor
  • Receptors, Progesterone
Topics
  • Carcinosarcoma (chemistry, metabolism, pathology)
  • Disease Progression
  • Estrogen Receptor alpha (analysis, biosynthesis)
  • Estrogen Receptor beta (analysis, biosynthesis)
  • Female
  • Humans
  • Microarray Analysis
  • Neoplasm Staging
  • Pilot Projects
  • Receptors, Growth Factor (analysis, biosynthesis)
  • Receptors, Progesterone (analysis, biosynthesis)
  • Signal Transduction
  • Uterine Neoplasms (chemistry, metabolism, pathology)

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