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1.
Soc Netw Anal Min ; 12(1): 78, 2022.
Article in English | MEDLINE | ID: mdl-36618491

ABSTRACT

Event detection using social media analysis has attracted researchers' attention. Prediction of events especially in the management of social crises can be of particular significance. In this study, events are predicted through analyzing Twitter messages and examining the changes in the rate of Tweets in a specified subject. In the proposed method, the Tweets are initially preprocessed in consecutive fixed-length time windows. Tweets are then categorized using the non-negative matrix factorization analysis and the distance dependent Chinese restaurant process incremental clustering. The categorization results show that a high rate of Tweets entering a cluster represents the occurrence of a new event in near future. Finally, a description of the event is presented in the form of some frequent words in each cluster. In this paper, investigations on a Tweet dataset during a 6-month period indicate that the rate of sending Tweets about predictable events considerably changes before their occurrence. The use of this feature can make it possible to predict events with high degrees of precision.

2.
Int J Organ Transplant Med ; 12(2): 50-52, 2021.
Article in English | MEDLINE | ID: mdl-34987739

ABSTRACT

Invasive aspergillosis (IA) is a severe complication after heart transplantation (HTx), with a high mortality rate. Invasive pulmonary aspergillosis (IPA) is the most common presentation. We herein describe a unique case of Renal aspergillosis (RAsp) diagnosed on month 10 post-HTx with no known risk factors for IPA in cardiac transplant recipients. The diagnosis of RAsp was made based on radiographic findings, renal biopsy, and tissue cultures. The patient initially received combined antifungal therapy (caspofungin and voriconazole) without radical or partial nephrectomy, followed by voriconazole maintenance monotherapy with favorable clinical outcomes.

3.
Int J Organ Transplant Med ; 12(4): 25-32, 2021.
Article in English | MEDLINE | ID: mdl-36570357

ABSTRACT

Background: Giardiasis is one of the opportunistic infections in immunocompromised patients, especially among organ transplant recipients. Objective: This study aimed to investigate the prevalence of Giardia lamblia infection in children with heart transplantation. Methods: A prospective cross-sectional study was conducted on 53 heart transplant recipients (aged 1-17 years). Transplant patients were on oral Trimethoprim/Sulfamethoxazole (TMP-SMX) from the first day of transplantation as a prophylaxis regimen. The prevalence of Giardia lamblia was evaluated on stool samples by phenotypic assay and polymerase chain reaction (PCR) method. Results: Out of 53 patients studied, 11 (20.75%) had gastrointestinal symptoms, and 42 (79.25%) were asymptomatic cases. No significant difference was observed between patients with and without gastrointestinal symptoms regarding type of heart disorders (p=0.13). The overall prevalence of Giardia lamblia infection among heart transplant patients was 5.7% (n=3). Moreover, the frequency was different between gastrointestinal symptomatic and asymptomatic recipients (27.27% and 0%, respectively). All three patients whose stool exams were phenotypically positive for Giardia lamblia were confirmed with PCR. Out of three, two Giardia lamblia isolates were found to have genotype B, while one isolate had genotype A. All of the Giardia positive patients suffered from chronic diarrhea and anorexia. Cryptosporidium spp., Isospora belli and Blastocysts spp. were not found in these cases. Conclusion: The incidence of Giardia lamblia infection in pediatric heart transplant patients is considerable and should be noted. A comprehensive guideline for the assessment of Giardia lamblia before and after transplantation is suggested.

4.
J Genet ; 992020.
Article in English | MEDLINE | ID: mdl-32661208

ABSTRACT

The number of gene mutations involved in the hereditary spastic paraplegias is rapidly growing due to the expansion of the frontiers of genomic research by next-generation DNA sequencing platforms. Nevertheless, a comprehensive genetic diagnosis method remains yet unavailable for these diseases. In the current research, an 8-year-old boy with short stature and developmental delay impairment, from a nonconsanguineous family, was referred to our genetic lab. Firstly, based on the physician recommendation, the patient was evaluated by tandem mass spectrometry (MS/MS) for the quantitative examination of amino acids, and then the patient was genetically investigated by karyotype analysis and whole-exome sequencing (WES) technique. Subsequently, targeted Sanger sequencing was applied to confirm the presence of the candidate variant in all the members of the family and screening the other patients for Troyer syndrome. Analysis of inherited metabolic disorders by tandem MS/MS showed the state of all the family members as normal and also karyotyping indicated no chromosomal aberration in the patient. Further investigation by WES technique indicated a homozygous missense variant in the SPG20 gene, c.1006C[T. Targeted sequencing result of the mutation confirmed homozygote state for the affected case and a heterozygote genotype for his parents. The mutation was classified as pathogenic. Detection of novel variants especially pathogenic variantin the SPG20 gene was associated with Troyer syndrome, which encodes a multifunctional protein termed Spartin, assist in improving genotype-phenotype correlation of genetic variants and may facilitate initial diagnosis of Troyer syndrome.


Subject(s)
Cell Cycle Proteins/genetics , Mutation, Missense , Spastic Paraplegia, Hereditary/genetics , Spastic Paraplegia, Hereditary/pathology , Child , Female , Humans , Male , Pedigree , Exome Sequencing
5.
Hum Antibodies ; 28(2): 169-178, 2020.
Article in English | MEDLINE | ID: mdl-32116244

ABSTRACT

Uropathogenic E. coli is one of the major agents of urinary tract infection. Today, no effective treatment or vaccine against this infection is exist. Accordingly, in the present study, a genetic constrruct for inducing of cellular immune system was designed. At first, fimH gene from E. coli 35218 was amplified using PCR. PCR product inserted into pET23a expression vector and the recombinant vector was analysed by sequencing. The vector was transformed to E. coli strain Origami and the protein was expressed under the 1 mM IPTG. FimH was purified with Ni-NTA column and the purified protein was used for immunization of BALB/c. Two weeks after the last injection, lymphocyte proliferation assay was carried out. In addition, IL-4 and IFN-γ cytokines, total antibody serum, IgG1 and IgG2a isotypes were quantified. Finally, protection ability of the vaccine in bladder and kidney infection of mice was evaluated.The results indicated that cellular immune response has a main protective role against UTI and FimH, as a vaccine candidate, significantly increase lymphocyte proliferation, IFN-γ response and total antibody amount. Immunization of mice with FimH conferred effective protection of kidney and bladder against urinary tract infection by uropathogenic E. coli (P< 0.002). It can be concluded that, the current FimH will be valuable for more trying to prepare a new vaccine against UTI.


Subject(s)
Adhesins, Escherichia coli/genetics , Adhesins, Escherichia coli/immunology , Fimbriae Proteins/genetics , Fimbriae Proteins/immunology , Immunity/immunology , Lectins/genetics , Lectins/immunology , Uropathogenic Escherichia coli/genetics , Uropathogenic Escherichia coli/immunology , Animals , Antibodies, Bacterial/immunology , Escherichia coli Infections/immunology , Female , Immunization/methods , Kidney/immunology , Kidney/microbiology , Lymphocytes/immunology , Lymphocytes/microbiology , Mice , Mice, Inbred BALB C , Urinary Bladder/immunology , Urinary Bladder/microbiology , Urinary Tract Infections/immunology , Urinary Tract Infections/microbiology
6.
Hum Exp Toxicol ; 39(8): 1031-1045, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32167384

ABSTRACT

Calprotectin is a heterodimeric EF-hand Ca2+ binding protein that is typically released by infiltrating polymorphonuclear leukocytes and macrophages. This protein is a key player linking inflammation and cancer. Due to the increased levels of calprotectin in different inflammatory diseases and cancer, it is considered as a marker for diagnostic purposes. In this study, we evaluated the mechanism of cell viability and apoptotic-inducing effects of recombinant human calprotectin (rhS100A8/S100A9) on the gastric adenocarcinoma (AGS), the most common type of gastric cancer cell line. AGS cells were exposed to the different concentrations (5-100 µg/ml) of calprotectin for 24, 48, and 72 h, and cell viability was assessed through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Apoptotic-inducing effects of calprotectin were evaluated by sub-G1 cell cycle assay and Annexin V/propidium iodide double staining. Furthermore, real-time polymerase chain reaction and Western blot analysis were performed to evaluate the mechanism of action of calprotectin. Our findings indicated that calprotectin inhibits growth and viability of AGS cells in a time- and dose-dependent manner. The half-maximal inhibitory concentration values were measured as 85.77, 79.14, and 65.39 µg/ml for 24, 48, and 72 h, respectively. Additionally, we found that calprotectin downregulated the expression of antiapoptotic protein Bcl-2 and upregulated proapoptotic protein Bax in a time- and concentration-dependent fashion. Calprotectin also slightly upregulated the expression of extracellular signal-regulated protein kinase 2 (ERK2), while it significantly decreased the levels of phospho-ERK in a time-dependent manner. Overall, these findings indicated that calprotectin has cytotoxicity and apoptosis-inducing effects on AGS cell lines in high concentration by modulating Bax/Bcl-2 expression ratio accompanied by inhibition of ERK activation.


Subject(s)
Adenocarcinoma/genetics , Calgranulin A/genetics , Calgranulin B/genetics , Mitogen-Activated Protein Kinase 1/genetics , Proto-Oncogene Proteins c-bcl-2/genetics , Stomach Neoplasms/genetics , Apoptosis , Cell Line, Tumor , Cell Survival , Down-Regulation/drug effects , Escherichia coli/genetics , Humans , Recombinant Fusion Proteins/genetics
7.
Hum Exp Toxicol ; 39(7): 960-972, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32096428

ABSTRACT

Although it has been widely considered that all-trans retinoic acid (ATRA) is an efficient therapeutic agent for acute promyelocytic leukemia (APL), there is an urgent need for extending and examining new therapeutics in medicine. Dithiocarbamates (DTCs) are one of the recent important chemical synthetic compounds used in cancer therapy. The aim of this study was to evaluate the apoptosis-inducing effect of 2-nitro-1-phenylethylpiperidine-1-carbodithioate (2-NDC) as an active derivative from DTCs, in combination with ATRA on human APL NB4 cells. The viability of treated NB4 cells was measured by 3-(4,5-dimethyltiazol-2-yl)-2,5-diphenyltetrazolium bromide assay in various concentrations (10-120 µM). The proapoptotic effects of 2-NDC were investigated by acridine orange/ethidium bromide staining, DNA ladder formation, and flow cytometry. We also assessed the oxidative stress-inducing effect of 2-NDC and in combination with ATRA on the NB4 cells. The alteration in gene expression levels of Bax, Bcl2, and Survivin was measured through a real-time polymerase chain reaction. Furthermore, we redetected the interaction between 2-NDC and antiapoptotic proteins Bcl2 and Survivin via molecular docking. We found that 2-NDC induced apoptosis in NB4 cells in a time-dosage-dependent manner. Also, 2-NDC triggered apoptosis by expanding intracellular reactive oxygen species, combined with ATRA. Bax/Bcl2 ratio was modulated and Survivin was downregulated in NB4 cells upon 2-NDC treatment. Molecular docking studies indicated that 2-NDC binds to the baculovirus inhibitor of apoptosis protein repeat domain of Survivin and Bcl homology 3 domain of Bcl2 with various affinities. Based on the present observations, it seems that this derivative can be estimated as an appropriate candidate for future pharmaceutical evaluations.


Subject(s)
Antineoplastic Agents/pharmacology , Leukemia, Promyelocytic, Acute/genetics , Proto-Oncogene Proteins c-bcl-2/genetics , Survivin/genetics , Thiocarbamates/pharmacology , Tretinoin/pharmacology , Apoptosis/drug effects , Cell Cycle/drug effects , Cell Line, Tumor , Cell Survival/drug effects , DNA Damage , Down-Regulation/drug effects , Drug Interactions , Humans , Leukemia, Promyelocytic, Acute/metabolism , Molecular Docking Simulation , Reactive Oxygen Species/metabolism
8.
Exp Oncol ; 41(4): 312-317, 2019 12.
Article in English | MEDLINE | ID: mdl-31868334

ABSTRACT

AIM: It has been reported that spiroaminopyrimidine derivatives inhibited the growth and proliferation of various cancer cell lines. In the present study, we evaluated cytotoxic and apoptosis-inducing effects of 2,4-diamino-1,3-diazaspiro[5.5]-9-tert-butyl-2, 4-diene-5-carbonitril (9-tBAP) on NB4 acute promyelocytic leukemia (APL) cells. MATERIALS AND METHODS: The cells were treated with 10-100 µM of 9-tBAP. Cytotoxic activity of the compound was measured using the MTT assay. Apoptosis was investigated by Hoechst 33258 staining as well as by Annexin V/PI double staining. RESULTS: The compound under study was found to be highly active cell growth inhibitor with IC50 of 30.0 ± 3.5 µM inducing apoptosis in NB4 cells. Cell cycle analysis by flow cytometry showed a time-dependent increase in sub-G1 cell population. Real-time polymerase chain reaction analysis revealed that the treatment with the compound down-regulated the BIRC5 expression in a time-dependent manner. CONCLUSION: 9-tBAP displayed potent anti-leukemic activity in vitro thus warranting further investigation.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Down-Regulation/drug effects , Leukemia, Promyelocytic, Acute/drug therapy , Pyrimidines/pharmacology , Survivin/genetics , Antineoplastic Agents/chemistry , Cell Line, Tumor , Cell Proliferation/drug effects , Humans , Leukemia, Promyelocytic, Acute/genetics , Leukemia, Promyelocytic, Acute/pathology , Pyrimidines/chemistry , Spiro Compounds/chemistry , Spiro Compounds/pharmacology
9.
J Mycol Med ; 29(1): 49-55, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30470620

ABSTRACT

OBJECTIVE: The effect of candidemia on immunologic parameters in breast tumor bearing patients is not well studied. Here, we hypothesised that candidemia in the tumor background may change the outcome of immunologic parameters and tumor condition. METHOD: Mice were divided into four groups, including normal, tumor, Candida infected (only Candidiasis) and tumor/Candidiasis groups. Tumor changes were recorded daily after tumor transplantation and induction of candidemia. Splenocytes of mice were harvested, cultured, and stimulated with PHA; afterwards, IL-4, IL-10, IFN-γ, TNF-α and TGF-ß cytokines were assessed using ELISA kits. We also evaluated the population of CD4+CD25+Foxp3+ regulatory T cells in the tumor infiltrated and splenocytes. RESULTS: The results showed that infection with C. albicans decreased the IFN-γ/IL-4 ratio in tumor/candidiasis and candidiasis groups versus their non-infected controls. IL-10, TGF-ß and TNF-α levels increased in the candidiasis group. In addition, Candidemia led to an increase in the Treg population in tumor microenvironment and splenocytes of experimental groups compared with non-infected controls. Finally, candidemia increased tumor growth of tumor/Candidiasis group compared with the tumor group. CONCLUSION: It seems that systemic infection with C. albicans could not only induce regulatory T cells but also result in dysregulation of cytokine network and thereby facilitate tumor growth.


Subject(s)
Breast Neoplasms/immunology , Candidemia/immunology , Cytokines/immunology , T-Lymphocytes, Regulatory/immunology , Animals , Breast Neoplasms/physiopathology , Candida albicans , Female , Interferon-gamma/immunology , Interleukin-10/immunology , Interleukin-4/immunology , Mice , Mice, Inbred BALB C , Spleen/cytology , Spleen/drug effects , Transforming Growth Factor beta1/immunology , Tumor Necrosis Factor-alpha/immunology
10.
J Urban Health ; 95(5): 682-690, 2018 10.
Article in English | MEDLINE | ID: mdl-29637433

ABSTRACT

Osteoporosis is a widespread disease among older peoples. The aim of this study is to estimate the prevalence of self-reported osteoporosis and assessing its association with socio-economic status. A population-based cross-sectional study was conducted in Tehran, Iran in 2011. Participants were 45,990 individuals aged above 20 years from 22 urban districts. Osteoporosis was measured by self-administrative questionnaire. Wealth index was constructed using principal component analysis based on household assets. Chi-square test, chi square test for trend, and crude odds ratio were used to assess associations in univariate analysis. Multiple logistic regression utilized to estimate adjusted associations between self-reported osteoporosis and socio-economic status.The overall estimated prevalence of self-reported osteoporosis was 4% (95% CI 3.88-4.13), 1.19% in men, and 6.84% in women (P < 0.001). The prevalence increased considerably as age increased (P for trend < 0.001). In multivariable analysis, education and wealth status were negative, and smoking was positively associated with the prevalence of self-reported osteoporosis. No association was found between participants' skill levels and Townsend deprivation index with the prevalence of self-reported osteoporosis.The findings of the present study have improved understanding of the association between socioeconomic status and osteoporosis in the Iranian population. It is important to consider socioeconomic status in screening and prevention programs.


Subject(s)
Osteoporosis/epidemiology , Self Report , Urban Population/statistics & numerical data , Adult , Aged , Aged, 80 and over , Cities/epidemiology , Cities/statistics & numerical data , Cross-Sectional Studies , Economic Status , Female , Humans , Iran/epidemiology , Logistic Models , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Population Surveillance , Prevalence , Social Class , Surveys and Questionnaires , Young Adult
11.
Hum Exp Toxicol ; 37(10): 1105-1116, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29430958

ABSTRACT

Recent studies have reported the potential of pyrano-pyridine compounds in inhibiting cell growth and apoptosis induction in cancer cells. Here, we investigated the effect of new pyrano-pyridine derivatives on proliferation, oxidative damages, and apoptosis in K562 leukemia cells. Among different tested compounds, we found 8-(4-chlorobenzylidene)-2-amino-4-(4-chlorophenyl)-5, 6, 7, 8-tetrahydro-6-phenethyl-4H-pyrano-[3,2-c]pyridine-3-carbonitrile (4-CP.P) as the most effective compound with IC50 value of 20 µM. Gel electrophoresis, fluorescence microscopy, and flow cytometry analyses indicated the apoptosis induction ability of 4-CP.P in K562 cells. Further analyses revealed that 4-CP.P induces significant increase in cellular reactive oxygen species production, lipid peroxidation, protein oxidation, and total thiol depletion. Interestingly, while 4-CP.P significantly increased the activity of superoxide dismutase, it reduced the catalase activity in a time-dependent manner. These data propose that 4-CP.P treatment causes free radicals accumulation that ultimately leads to oxidative stress condition and apoptosis induction. Therefore, we report the 4-CP.P as a novel, potent compound as a chemotherapeutic agent in cancer treatment.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Cell Survival/drug effects , Oxidative Stress/drug effects , Catalase/metabolism , Cell Proliferation/drug effects , Electrophoresis, Polyacrylamide Gel , Flow Cytometry , Humans , Inhibitory Concentration 50 , K562 Cells , Lipid Peroxidation/drug effects , Microscopy, Fluorescence , Oxidation-Reduction , Reactive Oxygen Species/metabolism , Sulfhydryl Compounds/metabolism
12.
Trop Biomed ; 35(1): 91-99, 2018 Mar 01.
Article in English | MEDLINE | ID: mdl-33601781

ABSTRACT

Echinococcus granulosus, the etiologic agent of echinococcosis, is one of the most important zoonotic helminthes worldwide. Knowledge of E. granulosus species and genotypes has important implications for epidemiology, control, and prevention of diseases as well as future vaccine and drug designs. There are many molecular methods developed to define genotypes of E. granulosus, among them high resolution melting (HRM) analysis, as a new approach, is a single step and closed tube method. It is appropriate for fast screening of large number of isolates. This technique is an accurate, user friendly, cost-effective, fast and simple method, which does not need post-PCR processes. Between March and lst august 2016, of 726 sheep examined in abattoirs in Razavi Khorasan province, Northeast Iran, 109 harboured cystic echincoccosis lesions (liver samples= 65 and lung samples= 44) which were collected for analysis. Total genomic DNA was extracted from each sample and amplified for the presence of polymorphism in the mitochondrial cox1 gene of Echinococcus granulosus using a high resolution melting curve (HRM) method. A total of 109 hydatid cyst samples analyzed by PCR high-resolution melting (qPCR-HRM) curve of the cox1 gene, all isolates were identified as G1 genotype (sheep strain). G1 is the predominant genotype in sheep in northeast of Iran. The high incidence of the G1 genotype (known to be the predominant E. granulosus genotype infecting humans globally) in sheep has considerable implications for hydatid disease control programs in this area.

13.
Microb Pathog ; 110: 457-463, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28739437

ABSTRACT

Exercise (with appropriate intensity and duration) is a natural modulator of immune responses and may be useful to increase the vaccine response towards antigen. According to the fact that rural area responding butter than urbon area to vaccine protocol, this study was undertaken to test the hypothesis that short term exercise training as an adjuvant for antigen such as herpes simplex virus type 1 (HSV-1) in animal models. Mice with/without access to short term exercise training were immunized intramuscularly with inactivated KOS strain of HSV-1. Immune responses was investigated with regards of both cell-mediated and humoral immunity. In this study by using short term exercise training as an adjuvant enhanced Th1 response while it did not show significant effect on Th2 responses towards HSV-1 immunization. Also, immunoglobulin G (IgG) 2a/IgG1-ratios increased in vaccine with short term exercise training group. These results suggested that coupling short term moderate exercise training as a mild adjuvant with vaccination may enhance cell-mediated immune responses especially Th1 responses.


Subject(s)
Herpesvirus 1, Human/immunology , Herpesvirus Vaccines/immunology , Immunity, Cellular , Physical Conditioning, Animal , Animals , Herpesvirus Vaccines/administration & dosage , Immunity, Humoral , Immunoglobulin G/blood , Injections, Intramuscular , Mice , Th1 Cells/immunology , Vaccines, Inactivated/administration & dosage , Vaccines, Inactivated/immunology
14.
Bratisl Lek Listy ; 118(4): 189-195, 2017.
Article in English | MEDLINE | ID: mdl-28471227

ABSTRACT

BACKGROUND AND OBJECTIVE: Hepatitis C virus (HCV) is a serious global health burden. There is no effective vaccine against HCV and new direct acting antivirals (DAAs) are so expensive and virtually unavailable to the public. Therefore, seeking for therapeutic or prophylactic vaccines is exigent and reliever. METHODS: The secondary and tertiary structures of the recombinant Core-NS3 (rC-N) fusion protein of HCV and its B and T-cells epitopes were evaluated with bioinformatics software. Cloning and in vitro expression of rC-N were performed by pET24a(+) and E.coli BL21-DE3 expression host, respectively. The recombinant protein purification was done by affinity chromatography method and then identified by Western blotting using anti-His monoclonal antibody. RESULTS: The sequences of rC-N protein consist of 1-118 amino acid parts of Core and 1095-1384 amino acids of NS3 were connected by a flexible linker (AAY) with proteasome cleavable site. The expressed and purified 46.7292 kDa rC-N protein had antigenic value up to threshold and conservancy found in this chimeric protein. Ramchandran Plot analysis represented that most residues were fallen in favourable regions. It also interacted with both type I and II major histocompatibility complex (MHC I, II) molecules. The rC-N had antigenic behaviour to create T cell responses. CONCLUSION: The results indicated that conserved rC-N protein had the ability to induce T-cell-mediated immune responses and it could be utilized as a therapeutic vaccine candidate against HCV (Tab. 3, Fig. 4, Ref. 40).


Subject(s)
Hepacivirus/immunology , Hepatitis C/therapy , Viral Hepatitis Vaccines/immunology , Viral Nonstructural Proteins/immunology , Hepatitis C/immunology , Hepatitis C/prevention & control , Humans , Immunotherapy/methods
15.
Cytokine ; 90: 100-108, 2017 02.
Article in English | MEDLINE | ID: mdl-27863332

ABSTRACT

Cancer cachexia is characterized by inflammation, loss of skeletal muscle and adipose tissue mass, and functional impairment. Oxidative stress and inflammation are believed to regulate pathways controlling skeletal muscle wasting. The aim of this study was to determine the effects of aerobic interval training and the purported antioxidant treatment, selenium nanoparticle supplementation, on expression of IL-15 and inflammatory cytokines in 4T1 breast cancer-bearing mice with cachexia. Selenium nanoparticle supplementation accelerated cachexia symptoms in tumor-bearing mice, while exercise training prevented muscle wasting in tumor-bearing mice. Also, aerobic interval training enhanced the anti-inflammatory indices IL-10/TNF-α ratio and IL-15 expression in skeletal muscle in tumor-bearing mice. However, combining exercise training and antioxidant supplementation prevented cachexia and muscle wasting and additionally decreased tumor volume in 4T1 breast cancer mice. These finding suggested that combining exercise training and antioxidant supplementation could be a strategy for managing tumor volume and preventing cachexia in breast cancer.


Subject(s)
Cachexia/immunology , Gene Expression Regulation, Neoplastic/immunology , Interleukin-10/immunology , Interleukin-15/immunology , Mammary Neoplasms, Experimental/immunology , Metal Nanoparticles , Muscle, Skeletal/immunology , Neoplasm Proteins/immunology , Physical Conditioning, Animal , Selenium/pharmacology , Tumor Necrosis Factor-alpha/immunology , Animals , Cachexia/pathology , Female , Mammary Neoplasms, Experimental/pathology , Mice , Mice, Inbred BALB C , Muscle, Skeletal/pathology
16.
Hum Exp Toxicol ; 36(3): 227-237, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27162247

ABSTRACT

The limited effectiveness of the conventional methods for cancer treatment makes the researchers to find novel safe and effective therapeutic strategies. One of these strategies is to use small interfering RNAs (siRNAs). A major challenge here is the siRNA delivery into the cells. The purpose of this study was to design and prepare a biocompatible, biodegradable, and safe nanosized particle for siRNA delivery into human breast cancer MCF-7 and leukemia K562 cells. Chemically synthesized magnetic nanoparticles containing polyethyleneglycol-lactate polymer (PEG-LAC), chitosan, and polyethyleneimine (PEI) were successfully prepared and used as a gene delivery vehicle. The nanoparticles were characterized by Fourier transform infrared spectroscopy and zeta potential. The Fe3O4-PEG-LAC-chitosan-PEI nanoparticle showed efficient and stable survivin siRNA loading in gel retardation assay. The cytotoxicity of the prepared nanoparticle was studied using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide assay and was compared with that of mitoxantrone (MTX) in combination with the prepared siRNA delivery system to evaluate the possible synergic effect of MTX and survivin siRNA. The nanoparticles with and without noncomplementary siRNA showed low toxicity against both cell lines; however, a twofold decrease was observed in cell survival percent after MTX addition to MCF-7 cells treated with either nanoparticle itself or complexed with noncomplementary siRNA. While survivin siRNA nanoplex caused threefold decrease in the cell survival percent, its combination with MTX did not result in a significant increase in the cytotoxic effect. Therefore, Fe3O4-PEG-LAC-chitosan-PEI nanoparticle should be considered as a potential carrier for enhanced survivin siRNA delivery into MCF-7 and K562 cells.


Subject(s)
Chitosan/chemistry , Ferrosoferric Oxide/chemistry , Inhibitor of Apoptosis Proteins/genetics , Nanoparticles/chemistry , Polyethylene Glycols/chemistry , Polyethyleneimine/chemistry , RNA, Small Interfering/administration & dosage , Cell Line, Tumor , Humans , Spectroscopy, Fourier Transform Infrared , Survivin
17.
Cell Stress Chaperones ; 21(5): 783-91, 2016 09.
Article in English | MEDLINE | ID: mdl-27245165

ABSTRACT

Impairment of adipose tissue and skeletal muscles accrued following type 1 diabetes is associated with protein misfolding and loss of adipose mass and skeletal muscle atrophy. Resistance training can maintain muscle mass by changing both inflammatory cytokines and stress factors in adipose tissue and skeletal muscle. The purpose of this study was to determine the effects of a 5-week ladder climbing resistance training program on the expression of Hsp70 and inflammatory cytokines in adipose tissue and fast-twitch flexor hallucis longus (FHL) and slow-twitch soleus muscles in healthy and streptozotocin-induced diabetic rats. Induction of diabetes reduced body mass, while resistance training preserved FHL muscle weight in diabetic rats without any changes in body mass. Diabetes increased Hsp70 protein content in skeletal muscles, adipose tissue, and serum. Hsp70 protein levels were decreased in normal and diabetic rats by resistance training in the FHL, but not soleus muscle. Furthermore, resistance training decreased inflammatory cytokines in FHL skeletal muscle. On the other hand, Hsp70 and inflammatory cytokine protein levels were increased by training in adipose tissue. Also, significant positive correlations between inflammatory cytokines in adipose tissue and skeletal muscles with Hsp70 protein levels were observed. In conclusion, we found that in diabetic rats, resistance training decreased inflammatory cytokines and Hsp70 protein levels in fast skeletal muscle, increased adipose tissue inflammatory cytokines and Hsp70, and preserved FHL muscle mass. These results suggest that resistance training can maintain skeletal muscle mass in diabetes by changing inflammatory cytokines and stress factors such as Hsp70 in skeletal muscle and adipose tissue.


Subject(s)
Adipose Tissue/metabolism , Cytokines/metabolism , Diabetes Mellitus, Experimental/metabolism , HSP70 Heat-Shock Proteins/metabolism , Muscle, Skeletal/metabolism , Animals , Diabetes Mellitus, Type 1/metabolism , Male , Physical Conditioning, Animal , Rats, Wistar , Resistance Training , Streptozocin
18.
J Endocrinol Invest ; 39(5): 515-22, 2016 May.
Article in English | MEDLINE | ID: mdl-26359145

ABSTRACT

INTRODUCTION: Diabetes mellitus is an important public health challenge worldwide. The prevalence of type 2 diabetes varies across countries. The aim of this study is to estimate the prevalence of type 2 diabetes and to determine related factors including socioeconomic factors in a large random sample of Tehran population in 2011. METHODS: In this cross-sectional study, 91,814 individuals aged over 20 years were selected randomly based on a multistage, cluster sampling. All participants were interviewed by trained personnel using standard questionnaires. Prevalence and Townsend deprivation indexes were calculated. Principal component analysis (PCA) was used to construct wealth index. Logistic regression model was used in multivariate analysis. RESULTS: The estimated prevalence of self-reported diabetes was 4.98 % overall, 4.76 %in men and 5.19 % in women (P < 0.003). In multivariate analysis, age, marital status (married and divorced/widow) and BMI were positively associated with the prevalence of self-reported diabetes. Of the socioeconomic variables, educational level and wealth status were negatively and Townsend Index was positively associated with diabetes. CONCLUSION: Our study findings highlight low reported prevalence of diabetes among adults in Tehran. Subjects with low socioeconomic status (SES) had a higher prevalence of type 2 diabetes. Weight gain and obesity were the most important risk factors associated with type 2 diabetes. Wealth index and educational level were better socioeconomic indicators for presenting the inequality in diabetes prevalence in relation to Townsend deprivation index.


Subject(s)
Diabetes Mellitus, Type 2/epidemiology , Self Report , Social Class , Adult , Aged , Cross-Sectional Studies , Female , Humans , Iran/epidemiology , Male , Middle Aged , Prevalence , Risk Factors , Young Adult
19.
Community Dent Health ; 33(3): 232-236, 2016 Sep.
Article in English | MEDLINE | ID: mdl-28509520

ABSTRACT

OBJECTIVE: To assess the prevalence of dental pain in the past year among adults in Tehran-Iran, and its determinants. BASIC RESEARCH DESIGN: Cross-sectional population study. PARTICIPANTS: A sample of 20,322 adults (18-64 years old). METHODS: A questionnaire survey was conducted across the 22 districts using the multi-stage random sampling method. Data were analysed applying the complex samples method. Multiple logistic regression analysis was used to adjust the effects of other variables on the outcome variable as dental pain in the past year. RESULTS: Overall, 19,645 individuals with a mean age of 39.9 (SD=12.5) years responded. Dental pain in the past year was reported by about one sixth (14%) of subjects and associated with being widowed/divorced (OR 1.45, 95%CI 1.07-1.97, p=0.016), married (OR 1.24, 95%CI 1.04-1.47, p=0.016), Azari minority (OR 1.2, 95%CI 1.05-1.37, p=0.009) and having dental visit in the past year (OR 2.6, 95%CI 2.29-2.95,p⟨0.001). Older subjects (OR 0.76, 95%CI 0.59-0.97, p= 0.029), those with a high economic status (OR 0.84, 95%CI 0.72-0.98, p=0.03), good (OR 0.75, 95%CI 0.58-0.96, p=0.023) or moderate oral health behaviour (OR 0.79, 95%CI 0.62-0.99, p=0.042), and good self-perceived oral health (OR 0.52, 95%CI 0.45-0.61, pp⟨0.001) were less likely to report dental pain. CONCLUSIONS: Dental pain in the past year was associated with being married/widowed, being a minority, and visiting a dentist in the past year. Older subjects and those with a high socio-economic status, good/moderate oral health behaviour, and good self-perceived oral health were less likely to report dental pain.


Subject(s)
Facial Pain/epidemiology , Adolescent , Adult , Cross-Sectional Studies , Female , Humans , Iran/epidemiology , Male , Middle Aged , Mouth Diseases/epidemiology , Prevalence , Risk Factors , Surveys and Questionnaires , Toothache/epidemiology
20.
Andrologia ; 47(1): 97-101, 2015 Feb.
Article in English | MEDLINE | ID: mdl-24456074

ABSTRACT

Infertility is the failure of a couple to engender after endeavouring at least one full year of unprotected intercourse. It has been reported that reactive oxygen species contributed to pathogenesis of various disease. To inactivate ROS cells biosynthesise several antioxidant enzymes, one of them is catalase which contributes H2 O2 to H2 O and O2 . This study set out to delineate the association of catalase C-262T polymorphism with idiopathic male infertility. The study included 195 men with idiopathic infertility and 190 healthy volunteers. Genomic DNA was extracted from peripheral blood leucocytes. Genotype and allele frequencies were determined in patients and controls using allele-specific PCR (AS-PCR). The prevalence of genotype frequencies of the CAT CC/CT/TT was 31.79%, 65.12% and 3.07%, respectively, in infertile subjects, as against 24.73%, 55.26% and 20%, respectively, in healthy volunteers. Statistical analysis has emerged significant difference from the comparison of either genotype (P < 0.05). Taking into accounts of results, the catalase C-262T polymorphism indicates that CAT-262T/T genotype confers less susceptibility to male infertility. Further studies with larger numbers of patients are required for further evaluation and confirmation of our finding.


Subject(s)
Asthenozoospermia/genetics , Catalase/genetics , Oligospermia/genetics , Adult , Case-Control Studies , Gene Frequency , Genetic Predisposition to Disease , Humans , Infertility, Male/genetics , Male , Polymorphism, Genetic
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