Trends in ovarian cancer incidence in Iran

Background: Cancer is amajorcause of morbidityandmortality,amongwhichovarian cancer has a high incidenceandcase fatality. Gaining insight into the epidemiology and trends of ovarian cancer can be very influential in cancer screening and treatments programming. This study aimed to investigate the trends in the incidence of ovarian cancer in Iran, because this issue has been neglected so far. Methods: This study is a re-analysis of existing data from the cancer data recording system in Iran during the years 2003 to 2009. The incidence rates reported were standardized according to the world health organization (WHO) and the trend in the incidence of this disease was determined by STATA software and the significance of the morbidity trend diagram was also derived via WINPEPI software. Results: The statistics of cancer registry center shows an increasing trend of ovarian cancer from 2003 to 2008, while it decreased from 2008 to 2009. During this period, 6078 cases of ovarian cancer were registered in Iran, increasing from 591 cases in 2003 to 1077 in 2009, which shows an approximately 2-fold increase in the incidence of registered cases. During these seven years, the highest incidence rate was seen in Markazi province with 6.33 per 100,000 persons and the least in Kohkiloye-va-Boyerahmad province with zero incidence. Almost all provinces, except a few, had increasing incidence of ovarian cancer. Conclusions: According to the results of the study, the incidence of ovarian cancer is increasing in Iran, especially in the central and northwestern regions of the country. This increase may be due to changing the patterns of risk factors for this disease, such as changes in lifestyle in the population, which will lead to changes in the incidence of the disease. Hence, due to the increase in incidence of this cancer, it is recommended to implement screening and early detection programs in high risk areas and populations. © 2016, Iranian Journal of Cancer Prevention

Hyperbranched polymers tune the physicochemical, mechanical, and biomedical properties of alginate hydrogels

The current research aimed to fabricate an alginate-hyperbranched polymer (HBP) complex, using a vortex fluidic device (VFD), to control the physicochemical, structural, and mechanical properties of alginate hydrogel; thus, providing a dominant biomaterial system for different biomedical applications. Samples were prepared by mixing alginate (6%w/w) with HBP (0.85 μM) before cross-linking with Ca2+ (100 mM). Magnet stirrer (600 rpm) and VFD (6000 rpm) were used to prepare experimental samples, and alginate was used as control. Comprehensive evaluations of bulk and surface morphology, microstructural analysis, swelling kinetics, mechanical characteristics, cytotoxicity, and formation of hydrogen bonds were conducted. The findings from this study revealed that the addition of HBP to alginate structure led to a higher swelling capability (86%), increased diffusion coefficient (66-fold), and enhanced failure mechanical properties (160% and 20% increases for failure stress and elongation at break, respectively) than control. Traditional mixing affected the surface morphology, while the bulk structure remained unchanged. Moreover, the rate of degradation was not significantly different between alginate and alginate-HBP samples. When VFD was incorporated, a higher swelling ratio (30%) was observed than the control sample and the coefficient of diffusion increased (34-fold). The associated degradation rate increased 30-fold, and the failure stress and elongation at break were increased 310% and 83%, respectively, compared to the control sample. The micromixing of alginate with HBP under high shear stress using a VFD created a micro-hybrid composite formed by alginate microparticles embedded in an alginate sheet

The Effect of Zoledronic Acid on BSP Expression and Methylation during Osteoblastic Differentiation of Mesenchymal Stem Cells

Background and Aim: Bone sialoprotein (BSP) is a specific marker of osteoblastic differentiation. In this research, the effect of Zoledronic Acid on BSP expression and methylation status during osteoblastic differentiation of mesenchymal stem cells (MSCs) was evaluated.Materials and Methods: In this experimental study, MSCs were isolated from human bone marrow. For osteogenic differentiation, hMSCs were pulse treated with zoledronic acid, and were incubated in osteogenic differentiation medium for 3 weeks. The DNA and RNA were extracted after the first, second and third weeks of culture and also from undifferentiated MSCs. After Sodium bisulfate (SBS) treatment, gene specific methylation analysis for BSP was carried out using Methylation Specific PCR technique.Results: BSP expression was observed in osteoblastic differentiated cells whereas it was not seen in MSCs. MSP showed that BSP was unmethylated during osteoblastic differentiation.Conclusion: BSP was expressed from the first week of differentiation. This confirms that zoledronic acid accelerates osteoblastic differentiation. Unmethylation status of BSP indicates that zoledronic acid does not have any effect on BSP methylation status. Other genetic or epigenetic mechanisms may control BSP expression during osteoblastic differentiation induction by zoledronic acid

Mouse oocyte vitrification: the effects of two methods on maturing germinal vesicle breakdown oocytes

Purpose Evaluation of viability and subsequent developmental ability of mouse germinal vesicle breakdown oocytes vitrified in conventional straws. Methods Oocytes with compact cumulus cells were cultured for 3 h in TCM199 medium GVBD and vitrified by two methods: the step-wise and single-step. After vitrification, the oocytes were thawed, and subjected to in vitro maturation and in vitro fertilization. Oocyte survival (postthaw) was assessed by morphological appearance and staining, using propidium iodide (PI)/Hoechst 33342. The oocyte maturation and fertilization rates were examined in vitro. Results In the single-step method the rates of post thaw survival, maturation to metaphase II and cleavage (2-cell embryos) were 58.68%, 56.41% and 38.63%, respectively. In the step-wise method, the corresponding rates were 81.75%, 68.59% and 51.80%, respectively. Conclusion Vitrification of mouse germinal vesicle breakdown oocytes by the step-wise method had the advantag