Background: Biofilm formation is one of the pathogenicity factors of Staphylococcus aureus that can help the bacteria to stick to the other surface and also increase antibiotic resistance pattern. This study aimed to investigate the phenotypic and genotypic indices for formating biofilm in Staphylococcus aureus isolates isolated from infectous samples.

Materials and Methods: 250 Staphylococcus aureus strains isolated from hospital infections were selected. Antibiotic resistance pattern was determined by using disk diffusion method. The ability of biofilm formation was investigated by molecular and phenotypic method.

Results: In this study, 73.5% of isolates were able to bind strongly, 5.33% had the ability of medium connection and 15.4% had the ability of weak connection in biofilm production. The frequency of icaC and icaB genes were 67.3% and 63.2%, respectively. 92.2% of biofilm producing isolates have mecA gene.

Conclusion: The spread of antibiotic resistance in isolates especially isolates that produce biofilm will create serious problems in the hospital therapeutic wards.

Background: Breast cancer is one of the major causes of cancer-related death and the most common solid malignancy in women worldwide. Chemerin as a new adipokine has an inflammatory activity that initiates inflammation via chemotaxis of immature DCs and macrophages. This study aimed to evaluate the level of chemerin in patients with breast cancer.

Materials and Methods: In this cross-sectional study that was performed as a case-control study, we enrolled 45 patients with breast cancer in Vali-asr hospital from June to December 2015 (age range, 18-60 years) and 40 healthy volunteers as a control group (age range, 22-56 years). The patients with invasive breast were selected before mastectomy. The level of serum chemerin was measured by ELISA kit.

Results: The results showed that the mean serum chemerin level in the breast cancer patients (1536 ±608 ng/L) was significantly lower than the normal individuals (1919±544 ng/L),(p=0.04). There is no correlation between the level of chemerin with body weight, stage of disease, duration of disease and the number of white and red blood cells.

Conclusion: With due attention to the inflammatory role of chemerin, decreasing the serum chemerin level in patients with breast cancer may be related to the consumption of chemerin in the inflammatory responses or immunosuppression by tumor. The low level of chemrerin may be suitable for tumor growth and progression.