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1.
Clinical and Experimental Reproductive Medicine ; : 54-60, 2020.
Article | WPRIM | ID: wpr-831367

ABSTRACT

Objective@#Oxidative stress plays a key role in the pathogenesis of male infertility. But, the adverse effects of oxidative biomarkers on sperm quality remain unclear. This study aimed to investigate the levels of nitric oxide (NO), 8-hydroxydesoxyguanosine (8-OHdG), and total antioxidant capacity (TAC) oxidative biomarkers in seminal plasma and their relationship with sperm parameters. @*Methods@#A total of 77 volunteers participated in the study, including fertile (n=40) and infertile men (n=37). NO, 8-OHdG, and TAC levels were measured using the ferric reducing ability of plasma, Griess reagent method and an enzyme-linked immunosorbent assay kit, respectively. @*Results@#The mean values of sperm parameters in the infertile group were significantly lower than those in the fertile group (p<0.001). The mean 8-OHdG in the seminal plasma of infertile men was significantly higher (p=0.013) than those of controls, while the mean TAC was significantly lower (p=0.046). There was no significant difference in NO level between the two groups. The elevated seminal 8-OHdG levels were negatively correlated with semen volume, total sperm counts and morphology (p<0.001, p=0.001 and p=0.052, respectively). NO levels were negatively correlated with semen volume, total sperm counts and morphology (p=0.014, p=0.020 and p=0.060, respectively). Positive correlations between TAC and both sperm count and morphology (p=0.043 and p=0.025, respectively) were also found. @*Conclusion@#These results suggested that increased levels of NO and 8-OHdG in seminal plasma could have a negative effect on sperm function by inducing damage to the sperm DNA hence their fertility potentials. Therefore, these biomarkers can be useful in the diagnosis and treatment of male infertility.

2.
Tehran University Medical Journal [TUMJ]. 2014; 72 (5): 301-306
in Persian | IMEMR | ID: emr-178175

ABSTRACT

Colorectal cancer is the third most common cancer in the world. Non-coding RNA especially miRNAs have important regulatory roles in cancer. miRNAs are small non coding RNA 21-23 nucleotides long which have different levels of expression between tumors and normal tissues. This study was designed to compare expression level of miRNA-21 between Iranian population colorectal cancer tissues and normal tissue. This case-control study has performed in medical genetics department of Tehran University of Medical Sciences from January to November 2013. We used 35 samples. The samples were isolated from tumor and adjacent normal tissues of colon. Thirty-five samples were divided into different groups according to cliniopathologic features including tumor size [>4 and <4 cm], metastasis [+ and -] and stage. After small RNA extraction from tissues by small RNA purification kit the quality and quantity of extracted RNA was determined using spectrophotometry. cDNAs were synthesized and real-time polymerase chain reaction carried out. Finally expression levels were statistically analyzed by LinRegPCR and REST software. miRNA-21 expression ratio in stages I, II and III were 1/804 and 4/574, respectively, the increase from stage III was statistically significant [P= 0.037]. The expression were also studied according to different clinicopathologic status of colon cancer, tumor size [>4 and <4 cm] and metastatic [+ and -], miRNA-21 over expressed in both groups, however the increase was not statistically significant. In this study, we found miR-21 over-expression in advanced stage in tumoral tissue comparing with normal adjacent tissue. This means perhaps in the future it would be possible to use miRNA-21 as an informative prognostic biomarker to guide for better treatment strategies for colorectal cancer patients. Our findings also indicate that miRNA-21 is a promising new molecular target for designing novel therapeutic strategies to control colorectal cancer


Subject(s)
Humans , MicroRNAs , Gene Expression , Case-Control Studies , Real-Time Polymerase Chain Reaction
3.
Tehran University Medical Journal [TUMJ]. 2014; 72 (2): 134-138
in Persian | IMEMR | ID: emr-195199

ABSTRACT

Background: A balanced reciprocal translocation is a structural abnormality, which at least consist of breakage of two non-homologous chromosomes along with pieces exchange and form quadrivalant structure that can produce unbalanced chromosomes during meiosis I and result in a fetus abortion. The aim of the present study is to offer using Preimplantation Genetic Diagnosis [PGD] 24sure array, which delivers aneuploidy screening of 24 chromosomes, within a few hours to increase fertility and bearing a child without chromosomal abnormality of this couple. This technique could replace embryo donation for child bearing of this couple


Case presentation: A young couple with recurrent pregnancy loss in 6th and 7[th] week of pregnancy without family history of recurrent miscarriage and any clinical signs had conferred. All laboratory tests including hormonal, infections, semen and hys-terosalpingography were normal except karyotype that showed balanced reciprocal translocation between chromosomes 5 and 18 in male. Chromosomal study of male parents showed normal karyotype


Conclusion: A balanced reciprocal translocation carrier is phenotypically normal, but during meiosis I, carrier chromosomes cant pair normally and form quadrivalant instead of bivalant that depend on type of their segregation [alternate, adjacent 1, adjacent 2,3:1,4:0], produce gametes that are chromosomally unbalanced which can result in early fetus abortion. Considering the number of abnormal gametes, the most effective way to help couples with this problem seems to be PGD 24sure, since it can identify reciprocal and Robertsonian translocation and allows concurrent screening of all chromosomes for aneuploidy. Another technique that can be compared with PGD 24sure is fluorescence in situ hybridization [FISH], but it has several technical limitations such as it is expensive and complexity, in addition it has only few probes [for chromosomes 21, 13, 18, X, Y] so sometimes necessary to create patient specific protocols

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