Effect of menstrual cycle and hormonal treatment on ki-67 and bcl-2 expression and adenomyosis
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Ki-67 and Bcl-2 expression in adenomyotic lesions increased during the proliferative phase and decreased in the luteal phase, with hormonal treatments showing varied effects.
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Abstract
OBJECTIVE: To study the expression of proliferation markers (ki-67) and anti-apoptotic protein (bcl-2) in adenomyotic lesions during the menstrual cycle or following the use of steroid hormones. PATIENTS AND METHODS: Ninety patients of reproductive age were included, who were submitted to endometrial resection for treatment of adenomyosis-related menorrhagia. Seven patients were using oral contraceptives and another seven had a levonorgestrel intrauterine device (IUD) (Mirena) in the uterine cavity at the time of the hysteroscopic procedure. Untreated patients were divided into four groups: menstruation/early proliferative phase (n = 24), late proliferative (n = 19), early luteal phase (n = 7) and late luteal phase (n?=?26). Bcl-2 and ki-67 expression was determined in paraffin-embedded tissue blocks using immunohistochemical methods. RESULTS: Proliferation rates in adenomyotic lesions increased during the proliferative phase, reaching a peak during ovulation to decrease to values close to zero in the late luteal phase. Bcl-2 expression showed a similar curve with peak values during the later proliferative phase followed by a significant decrease in the number of cases showing strong positive expression in the late luteal phase. Both Mirena and oral contraceptives decreased ki-67 expression on adenomyosis but only Mirena was affective in diminishing bcl-2 expression. CONCLUSION: During the luteal phase, both ki-67 and bcl-2 expression is reduced in adenomyotic lesions in a similar way to that occurring in patients using Mirena. Oral contraceptives, on the other hand, do not affect bcl-2 expression in adenomyosis.
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References (7)
- Adenomyosis: Diagnosis by Hysteroscopic Endomyometrial Biopsy, Correlation of Incidence and Severity with Menorrhagia via openalex
- Apoptosis and Ki-67 expression in adenomyotic lesions and in the corresponding eutopic endometrium via openalex
- Effects of the levonorgestrel-releasing intrauterine system on proliferation and apoptosis in the endometrium via openalex
- Efficacy of the levonorgestrel intrauterine system in treating menorrhagia: Actualities and ambiguities via openalex
- Medical treatment of a grossly enlarged adenomyotic uterus with the levonorgestrel-releasing intrauterine system via openalex
- W2157162135 via openalex
- W2164135151 via openalex
Cited by (12)
- The expression of <i>BECN1, LC3B</i> , and <i>BCL2</i> genes in eutopic endometrium of patients with adenomyosis: A cross-sectional study 2021
- Bioinformatics strategy for the screening of key genes to differentiate adenomyosis from endometriosis (Review) 2019
- Adenomiosis: tratamiento 2015
- Constitutive and tumor necrosis factor-α-induced activation of nuclear factor-κB in adenomyosis and its inhibition by andrographolide 2013
- Expression of heme oxygenase in the eutopic and ectopic endometrium in patients with adenomyosis 2012
- Elevated immunoreactivity to tissue factor and its association with dysmenorrhea severity and the amount of menses in adenomyosis 2010
- Promoter Hypermethylation of Progesterone Receptor Isoform B (PR-B) in Adenomyosis and Its Rectification by a Histone Deacetylase Inhibitor and a Demethylation Agent 2010
- Laparoscopic excision of uterine adenomyomas 2007
- Tratamiento de la adenomiosis 2007
- Traitement de l'adénomyose 2007
- Medical and surgical management of adenomyosis 2006
- 10.1016/s0246-1064(14)65366-4 2000
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