دورية أكاديمية

Differential regulation of Akt phosphorylation in endometriosis.

التفاصيل البيبلوغرافية
العنوان: Differential regulation of Akt phosphorylation in endometriosis.
المؤلفون: Cinar, Ozgur1, Seval, Yasemin1,2, Uz, Yesim H.1,3, Cakmak, Hakan1, Ulukus, Murat1,4, Kayisli, Umit A.1, Arici, Aydin1 aydin.arici@yale.edu
المصدر: Reproductive BioMedicine Online (Reproductive Healthcare Limited). Dec2009, Vol. 19 Issue 6, p864-871. 8p.
مصطلحات موضوعية: *PROTEIN kinases, *APOPTOSIS, *ESTROGEN, *ESTRADIOL, *ENDOMETRIUM
مستخلص: Protein kinase B (PKB/Akt), a serine/threonine kinase, regulates the function of many cellular proteins involved in apoptosis and proliferation. It was postulated that there is a higher Akt activity in endometriosis compared with normal endometrium, and that oestrogen may be one of the factors responsible for the high Akt activation in endometriotic cells. Phospho-Akt (pAkt) concentrations in normal, eutopic and ectopic endometrial tissues were compared by immunohistochemistry, and a higher pAkt immunoreactivity was revealed in eutopic and ectopic endometrium compared with normal endometrium, in vivo. Higher Akt phosphorylation in stromal cells from eutopic endometrium was observed, when compared with normal, in vitro (P < 0.05). Akt phosphorylation was rapidly (2-10 min) stimulated when endometrial stromal cells from normal and endometriosis patients were treated with 17b-oestradiol. In endometrial stromal cells from the endometriosis group, ICI 182,780 (ICI, a specific oestrogen receptor antagonist) failed to antagonize the effect of oestradiol when combined with oestradiol, and revealed a stimulatory effect on Akt phosphorylation when given alone (P < 0.05). In conclusion, since Akt affects cell survival, it is suggested that increased Akt phosphorylation may be related to the altered apoptosis/proliferation harmony in endometriosis, and therefore Akt may play a critical role in the pathogenesis of endometriosis. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:14726483
DOI:10.1016/j.rbmo.2009.10.001