Effect of tamoxifen treatment on the epidermal growth factor receptor expression in the mouse ovarian tissue
Öz
The objective of this study was to investigate the effect of Tamoxifen (TAM) treatment on epidermal growth factor receptor (EGFR) expression in the pubertal mice ovary. In this study, 80 female mice (8 week-old) were used. Animals divided four groups; non-injected (control A), injected with TAM’s vehicle solution (control B). The mice in groups TAM 0.5 and TAM 1.5 were treated with tamoxifen at a dose 0.5 and 1.5 mg/mouse/day respectively. TAM was dissolved with 10% ethanol: 90% corn oil. Mice were given daily subcutaneously injections for 5 days. Ovarian sections were immunostained with EGFR antibody and triple staining for examine the general structure. We observed that follicular atresia was increased, follicular cysts were formed in stroma, and interstitial cells were increased with TAM dose treatment. In the present study, there were no significant differences in the EGFR expression in mouse ovary of all groups. EGFR expression was not determined in the granulosa cells. While strong EGFR immunoreaction was observed in the interstitial cells and oocyte cytoplasma, weak EGFR immunoreactions was observed in theca cells of follicles.
As a result, it was observed that the administered doses of TAM have not significant influence on EGFR expression.
Anahtar Kelimeler
Kaynakça
- 1. Arteaga CL. Epidermal growth factor receptor dependence in human tumors: more than just expression? Oncologist, 4: 31-39, 2002.
- 2. Ashkenazi H, Cao X, Motola S, Popliker M, Conti M, Tsafriri A. Epidermal growth factor family members: endogenous mediators of the ovulatory response. Endocrinology, 146: 77-84, 2005.
- 3. Atalay G, Cardoso F, Awada A, Piccart MJ. Novel therapeutic strategies targeting the epidermal growth factor receptor (EGFR) family and its downstream effectors in breast cancer. Ann Oncol, 14: 1346-1363, 2003.
- 4. Ayyagari RR, Khan-Dawood FS. Human corpus luteum: presence of epidermal growth factor receptors and its binding characteristics. Am J Obstet Gynecol, 150: 942-946, 1987.
- 5. Bernstein L, Deapen D, Cerhan JR. Tamoksifen therapy for breast cancer and endometrial cancer risk. J Natl Cancer Inst, 91: 1654–1662, 1999.
- 6. Blumenfeld Z, Dann E, Avivi R, Epelbaum R, Rowe JM. Fertility after treatment for hodgkin’s disease. Ann Oncol, 13: 138-147, 2002.
- 7. Clarke M, Cillins R, Davies C. Tamoksifen for early breast cancer: an overview of the randomized trials. Lancet, 351: 1451-1467, 1998.
- 8. Crossmonn GA. Modification of Mallory’s Connective Tissue stain with a discussion of the principles ınvolved. Anat Rec, 69(1): 33-38, 1937.
Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
Araştırma Makalesi
Yayımlanma Tarihi
15 Ekim 2018
Gönderilme Tarihi
16 Nisan 2018
Kabul Tarihi
13 Haziran 2018
Yayımlandığı Sayı
Yıl 2018 Cilt: 37 Sayı: 2