These results are also supported by the cell cycle analysis which showed very weak

effects on the stromal cells, only at 72 hrs at the highest concentration (Figure  6E-F). Figure 6 Effects of purified CH5183284 recombinant protein of Homo Sapiens anti-Mullerian hormone (AMH) digested by Plasmin from human plasma on endometriosis stromal and epithelial cell line. (A) pre-G1 fraction analysis of endometriosis stromal cells treated for 24-48-72 hrs with the final concentrations of cleaved MIS as indicated. The data are shown in a time-dependent manner. (B) pre-G1 fraction analysis of endometriosis stromal cells treated for 24-48-72 hrs with the final concentrations of cleaved MIS as indicated. The data are shown in a dose-dependent manner. (C) Cell cycle analysis of endometriosis stromal cells treated for 24-48-72 hrs with the final concentrations of cleaved MIS as indicated. The data are shown in a time-dependent manner. (D) Cell cycle analysis of endometriosis stromal cells treated for 24-48-72 hrs with the final concentrations of cleaved MIS as indicated. The data click here are shown in a dose-dependent manner. (E) pre-G1 fraction analysis of endometriosis epithelial cells treated for 24-48-72 hrs with 1000 ng/mLof cleaved MIS. The data are shown in a time-dependent manner.

(F) Cell cycle analysis of endometriosis epithelial cells treated for 24-48-72 hrs with 1000 ng/mLof cleaved MIS. The data are shown in a time-dependent manner. Discussion Endometriosis is a benign disease of women during reproductive age [17];

nevertheless, it is well known that endometriosic cells display functional properties that are typical of neoplastic cells, such as crotamiton anti-apoptotic, invasive and metastatic capacities [18, 19]. In support to this observation, epidemiological studies have shown that there exists an increased risk of different types of malignancies, especially ovarian cancer and non-Hodgkin’s lymphoma in women with endometriosis [20, 21]. Nevertheless, it has been reported an association between endometriosis, dysplastic nevi, melanoma, and breast cancer [22, 23]. Finally, several histological and genetic studies have indicated that endometriosis may transform into cancer or that it could be considered a this website precursor of cancer [24]. Recently, it has been demonstrated by Wang et al., that adult human endometrium has a functional AMH/AMHRII signal transduction system and that the activation of this system is able to negatively regulate cellular viability in cultured endometrial cells [12]. Indeed, the exact biological role of AMH in adult females is unclear. The most well recognized function in adult is its involvement in recruitment and selection of initial primordial follicles [25]. In fact, there exists a plethora of research articles on the use of AMH serum level as a sensitive marker to assess the ovarian reserve [26].