ObjectivesObesity is a significant risk factor for a number of chronic diseases, including diabetes, cardiovascular diseases, and cancer. Obesity usually results from a combination of causes and contributing factors, including genetics and lifestyle choices. Many studies have shown an association of single nucleotide polymorphisms (SNPs) in the fat mass and obesity-associated (FTO) and the melanocortin-4 receptor (MC4R) genes with body mass index (BMI). Therefore, recognizing the main genes and their relevant genetic variants will aid prediction of obesity risk. The aim of our study was to investigate the frequency of rs9939609 and rs17782313 polymorphisms in FTO and MC4R genes in an Iranian population.MethodsWe enrolled 130 obese patients and 83 healthy weight controls and calculated their BMI. Genomic DNA was extracted from peripheral blood and the frequency of rs9939609 and rs17782313 polymorphisms in FTO and MC4R genes was determined using the tetra-primer amplification refractory mutation system-polymerase chain reaction (ARMS-PCR).ResultsSignificant associations were found between FTO rs9939609 and BMI. Where homozygous risk allele carriers (A-A) have significant higher odds ratio (OR) of being obese than individuals with normal BMI (OR = 6.927, p < 0.005, 95% confidence interval (CI): 3.48–13.78). No significant correlation between MC4R rs17782313 and obesity were observed when compared to healthy weight individuals. Although subjects with C-C genotype had higher odds of obesity (OR = 1.889, p = 0.077, 95%CI: 0.92–3.84).ConclusionsThis study shows a relationship between FTO polymorphism and increased BMI, therefore, SNP in the FTO gene influence changes in BMI and can be considered a prognostic marker of obesity risk.

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C olorectal cancer has become predominant cancer and now accounts for approximately 10% of cancer-related mortality in western countries (Kuipers et al., 2015). Colorectal cancer is the second-and third-most common cancer in women and men, respectively (Kuipers et al., 2015, Kuipers et al., 2013). Colorectal cancer (CRC) is the third most common mortality factor in Iran (Dolatkhah et al., 2015). The rate of an outbreak of CRC depended on the geographical regions (Khosravi Shadmani et al., 2017, Dolatkhah et al., 2015, Johnson et al., 2013). A high incidence of CRC has been observed in developed nations, such as the US, and Canada, and developing countries also continue increasing outbreak rates (Jemal et al., 2010, Khosravi Shadmani et al., 2017). In Iran, the prevalence of the CRC has experienced the same growth as those of other Asian nations, with CRC accounting for 8.4% of all research Article Abstract | Background: Colorectal cancer is one of the most common cancers in Iran. There are many effective methods of treatment of it. As a conventional treatment, chemotherapy has become a part of treatment scheme for patients with colorectal cancer. Enterococci are intestinal commensals. They are opportunistic pathogens which cause millions of human and animal infections annually. The aim of this study was to investigate the side effects of chemotherapy of sufferers from colon cancer on the antibiotic resistance of microflora. Methods: In this study, participants were divided into three groups: Group A: 300 colorectal cancer patients before the start of the cancer chemotherapy, group B: 300 healthy people living with patients at least for recent 12 months and group C includes 300 patients with colorectal cancer after six weeks chemotherapy. RNA was extracted from the stool of all the participants of the study. Following the RNA extraction from stool samples, cDNA libraries were constructed. Eight virulent genes (vanA, vanB, gelE, esp, asa1, aggA, efaA and enlA) of E. faecalis were evaluated by real-time qPCR. results: The results were showed the expression level of the virulent genes in the group of the patients after chemotherapy was significantly higher than the two groups of B and C (P<0.05). Although the expression of these genes in the group of patients before chemotherapy was higher than that of the control group, this increase was not significant (P>0.05). conclusions: It seems that chemotherapy could change the balance of mRNA expression of microflora such as antibiotic resistance genes. These could be responsible for infections arisen after ending the chemotherapy of cancer.

many forms ranging from a loss in well-defined patches (AA), or diffuse hair loss in the form of total loss of scalp hair called alopecia totalis (AT), or loss of entire scalp and body hair called alopecia universalis (AU), which can affect all hair-bearing sites. Patchy alopecia affecting the scalp is the most common type (

Prostate cancer is the most prevalent and second cause of death from cancer in men worldwide. Immunotherapy is a new method for the treatment of several cancers that fights cancer cells by strengthening the immune system through some medications. While immunotherapy is a useful method for cancer treatment; its side effects still are not totally clarified. Numbers of prostate cancer patients which take immunotherapy are experiencing prostate inflammation and prostatitis after treatment period. Enterococcus faecalis is Gram-positive and catalase-negative cocci that are common in the intestines of humans and other animals and cause most enterococcal infections such as intestinal infections, prostatitis, gastroenteritis and endocarditic. Present study aimed to evaluate the mRNA level of virulence genes which are involved in Enterococcus faecalis pathogenesis in prostate cancer patients that treated by immunotherapy. Expression level of gelatinase E (gelE) and Enterococcal surface protein (esp) genes were examined by Real time PCR in three groups of 68 male subjects. Group A normal subjects, group B prostate cancer patients before start treatment and group C prostate cancer patients after six months immunotherapy period. Results were showed significant (P<0.05) over expression of both genes (gelE and esp ) in group C against the group B. According to the results, it is reasonable that immunotherapy may have side effects such as increasing the pathogenicity risk of microflora in patients. Maybe these side effects could cause further infections after ending the immunotherapy of cancer. Antibiotic usage after or at the same time of immunotherapy period could prevent possible infections of microflora including E. faecalis.