Journals / Uzmanlık Sonrası Eğitim ve Güncel Gelişmeler Dergisi / 2007 / Cilt: 4 - Sayı: 2

Fas expression in endometriomas, endometrioid carcinomas and clear cell carcinomas of ovaries

Endometriomalar ile overin endometrioid ve berrak hücreli karsinomlarında fas ekspresyonu

Pages
108–113
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In conclusion, we suggest that in endometriosis related ovarian tumors apoptotic mechanisms might be more impaired than endometriomas and also decreased expression of Fas might be involved in the malign transformation of endometriosis.

📌 3 Key Takeaways

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Objective & Hypothesis:In this study we aimed to investigate the expression of Fas protein by immunohistochemistry between ovarian endometriomas and endometriosis related ovarian tumors, endometrioid and clear cell carsinomas.
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Key Findings & Data:Ovarian endometriosis (n = 22), ovarian endometrioid adenocarsinomas (n = 12) and ovarian clear cell carsinomas (n =8) histopathologic samples were included in this study.
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Conclusion & Impact:In conclusion, we suggest that in endometriosis related ovarian tumors apoptotic mechanisms might be more impaired than endometriomas and also decreased expression of Fas might be involved in the malign transformation of endometriosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Yumurtalık neoplazmları · İmmünohistokimya · Apoptoz

Abstract

In this study we aimed to investigate the expression of Fas protein by immunohistochemistry between ovarian endometriomas and endometriosis related ovarian tumors, endometrioid and clear cell carsinomas. Ovarian endometriosis (n = 22), ovarian endometrioid adenocarsinomas (n = 12) and ovarian clear cell carsinomas (n =8) histopathologic samples were included in this study. When we compared the epithelial Fas expression among three groups, we observed that endometriomas express significantly higher epithelial Fas than both ovarian tumors (P< 0.001). In conclusion, we suggest that in endometriosis related ovarian tumors apoptotic mechanisms might be more impaired than endometriomas and also decreased expression of Fas might be involved in the malign transformation of endometriosis.

Özet

Bu çalışmada ovaryan endometriomalar ve endometriozisle ilişkili oldukları bilinen overin endometrioid ve berrak hücreli karsinomlarının Fas protein ekspresyonu yönünden immünohistokimyasal yöntemle karşılaştırılmasını amaçladık. Çalışmaya ovaryan endometriyozis (n = 22), overin endometrioid adenokarsinomu (n = 12) ve overin berrak hücreli karsinomu (n = 8) tanısı alan toplam 42 olgu dahil edilmiştir. Her üç grubu epitelyal Fas ekspresyonu açısından kıyasladığımızda endometriyomalı olguların her iki tipteki over karsinomlu olgulara göre istatistiksel olarak daha fazla Fas proteini eksprese ettiklerini gösterdik (P < 0.001). Sonuç olarak endometriomalara kıyasla endometriozisle ilişkili over tümörlerinde apoptozis mekanizmalarının daha da bozulmuş olabileceği ve endometriozisin malign transformasyonuna azalmış Fas proteininin de katkıda bulunabileceği ileri sürülebilir.

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Cite This Article

ULUKUŞ, M., ÇIRPAN, T., TEREK, C., GÖK, M., ULUKUŞ, Ç., ZEKİOĞLU, O., DİKMEN, Y., DİNÇER, Ö. (2007). Fas expression in endometriomas, endometrioid carcinomas and clear cell carcinomas of ovaries. Uzmanlık Sonrası Eğitim ve Güncel Gelişmeler Dergisi, Cilt: 4 - Sayı: 2, 108–113. https://ajindex.com/articles/320553

References (19)

  1. Hamle J, Hammond MG, Hulka JF, Raj SG, Talbert LM. Retrograde menstruation in healthy women and in patients with endometriosis. Obstet Gynecol 1984;64:151-54
  2. Mülayim N, Arici A. The relevance of the peritoneal fluid in endometriosis-associated infertility. Hum Reprod 1999;14 supp 2:67-76
  3. Hill JA, Faris HMP, Schiff I, Anderson DJ. Characterization of leukocytes subpopulations in the peritoneal fluid of women with endometriosis. Fertil Steril 1988;50:216-22
  4. Kennedy S, Mardon H, Barlow D. Familial endometriosis. J Assist Reprod Genet 1995;12:32-34
  5. Noble LS, Simpson ER, Johns A, Bulun SE. Aromatase expression in endometriosis. J Clin Endocrinol Metab. 1996;81:174-79
  6. Mayani A, Barel S, Soback S, Almagor M. Dioxin concentrations in women with endometriosis. Hum Reprod 1997;12:373-75
  7. Lebovic DI, Mueller MD, Taylor RN. Immunobiology of endometriosis. Fertil Steril 2001;75:1-10
  8. Ulukus M, Arici A. Immunology of endometriosis. Minerva Ginecol 2005;57:237-48
  9. Harada T, Iwabe T, Terakawa N. Role of cytokines in endometriosis. Fertil Steril 2001;76:1-10
  10. Heaps JM, Nieberg RK, Berek JS. Malignant neoplasms arising in endometriosis. 1990;75:1023-28
  11. Stern RC, Dash R, Bentley RC, Snyder MJ, Haney AF, Robboy SJ. Malignancy in endometriosis: frequency and comparison of ovarian and extraovarian types. Int J Gynecol pathol 2001; 20:133-39
  12. Fauvet R, Poncelet C, Hugol D, Lavaur A, Feldmann G, Darai E. Expression of apoptosis-related proteins in endometriomas and benign and malignant ovarian tumors. VirchowsArch 2003; 443:38-43
  13. Harada T, Kaponis A, Iwabe T, Taniguchi F, Makrydimas G, Sofikitis N, Paschopoulos M, Paraskevaidis E, Terakava N. Apoptosis in human endometrium and endometriosis. Hum Reprod Update 2004;10:29-38
  14. Hefler L, Mayerhofer K, Nardi A, Reinthaller A, Kainz C. Serum soluble Fas levels in ovarian cancer. Obstet Gynecol 2000;96:65-9
  15. Garcia-Velasco J, Arici A, Zreick T, Naftolin F, Mor G. Macrophage- derived growth factors regulate FasL expression in endometrial cells:a role in endometriosis. Mol Hum Reprod 1999;5:642- 50
  16. Nagata S, Golstein P. The Fas death factor. Science 1995;267: 1449-56
  17. American Fertility Society. Revised American Fertility Society clssification of endometriosis. Fertil Steril 1985;43:351
  18. Brinton LA, Gridley G, Persson I, Baron J, Bergqvist A. Cancer risk after a hospital discharge diagnosis of endometriosis. Am J Obstet Gynecol 1997;176:572-79
  19. Nishida M, Watanabe