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  1. Article ; Online: Investigating the Relationship between the Levels of IL18, RANKL Gene Expression, MicroRNA-146a and Inflammatory Factors with the Severity of COVID-19.

    Hamad Khdhir, Karmand / Alipour, Shahriar / Gholizadeh-Ghaleh Aziz, Shiva / Banihashemi, Seyed Hesamaddin

    Iranian journal of allergy, asthma, and immunology

    2023  Volume 22, Issue 1, Page(s) 82–90

    Abstract: COVID-19 can induce lung inflammation, and inflammatory factors play an essential role in its pathogenesis. This inflammation can be controlled to a great extent by microRNAs(miRs). This study evaluated miR-146a-5p expression levels in the serum of ... ...

    Abstract COVID-19 can induce lung inflammation, and inflammatory factors play an essential role in its pathogenesis. This inflammation can be controlled to a great extent by microRNAs(miRs). This study evaluated miR-146a-5p expression levels in the serum of patients with COVID-19 and their association with the expression of interleukin (IL)-18 and receptor activator of nuclear factor kappa-Β ligand (RANKL) genes, and lung damage. patients with COVID-19 were divided into two groups: mild and severe phases. The severe phase is defined as having a positive polymerase chain reaction (PCR) for SARS-CoV2, and acute pulmonary symptoms. The subjects' demographic, clinical, and paraclinical characteristics were collected according to a pre-prepared checklist. Total RNA was isolated from all samples using the Trizol kit to assess gene expression. The extracted product was then evaluated for the expression of miR-146a and the target genes (i.e., IL-18 and RANKL) using real-time PCR. The miR-146a gene's mean expression in mild and severe patients was 0.73 and 1.89, respectively, and this difference was statistically significant between the two groups. Also, the mean Expression of the IL-18 gene, 1.37±0.38 in the mild and 2.83±0.58 in the severe groups of the disease, demonstrated a significant difference between the two groups. In contrast, the expression levels of the RANKL gene did not show a significant difference between the two groups. Therefore, it may be hypothesized that altered levels of miR-146a may contribute to the severe COVID-19 that is more commonly observed in smokers, but further research is required.
    MeSH term(s) Humans ; COVID-19/blood ; COVID-19/epidemiology ; COVID-19/pathology ; Male ; Female ; Middle Aged ; Aged ; Patient Acuity ; MicroRNAs/blood ; RANK Ligand/blood ; Interleukin-18/blood ; Lung/pathology ; Lung/virology ; Biomarkers/blood ; Iran/epidemiology
    Chemical Substances MIRN146 microRNA, human ; MicroRNAs ; RANK Ligand ; Interleukin-18 ; IL18 protein, human ; TNFSF11 protein, human ; Biomarkers
    Language English
    Publishing date 2023-02-20
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2488724-9
    ISSN 1735-5249 ; 1735-1502
    ISSN (online) 1735-5249
    ISSN 1735-1502
    DOI 10.18502/ijaai.v22i1.12009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Alantolactone and ZnO nanoparticles induce apoptosis activity of cisplatin in an ovarian cancer cell line (SKOV3).

    Alipour, Shahriar / Babaei, Ghader / Gholizadeh-Ghaleh Aziz, Shiva / Abolhasani, Somayeh

    Research in pharmaceutical sciences

    2022  Volume 17, Issue 3, Page(s) 294–304

    Abstract: Background and purpose: Ovarian cancer is one of the leading causes of cancer mortality in women. Despite the increase in cases of this cancer, the current therapeutic strategy is not effective. This study aimed to investigate the effect of cisplatin ( ... ...

    Abstract Background and purpose: Ovarian cancer is one of the leading causes of cancer mortality in women. Despite the increase in cases of this cancer, the current therapeutic strategy is not effective. This study aimed to investigate the effect of cisplatin (Cis) with alantolactone (ALT) and ZnO nanoparticles (ZnONPs) in inducing apoptosis in SKOV3 ovarian cancer cells line.
    Experimental approach: To evaluate the viability of SKOV3 cells and determine the IC
    Findings / results: Our results showed that ALT and ZnONPs significantly increased the response to Cis in SKOV3 cells compared to the control and this response is remarkably increased in the triple combination (ALT-Cis-ZnONPs). The expression of XIAP, cyclin D1, and Bcl-2 genes and proteins in the groups treated with ALT, Cis, and ZnONPs as a single agent, double and triple combination were significantly reduced compared to the control, while Bax was generally shown an increase. Also, the level of intracellular ROS is higher in the treatment groups than in the control group and the highest increase was observed in the triple combination.
    Conclusion and implications: Taken together, our data demonstrated the potential therapeutic approach of using ALT and ZnONPs that may enhance the apoptotic effects of Cis on the SKOV3 cells.
    Language English
    Publishing date 2022-04-18
    Publishing country Iran
    Document type Journal Article
    ZDB-ID 2400156-9
    ISSN 1735-9414 ; 1735-5362
    ISSN (online) 1735-9414
    ISSN 1735-5362
    DOI 10.4103/1735-5362.343083
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Evaluating the effect of Alantolactone on the expression of N-cadherin and Vimentin genes effective in epithelial-mesenchymal transition (EMT) in breast cancer cell line (MDA-MB-231).

    Naderi, Roya / Gholizadeh-Ghaleh Aziz, Shiva / Haghigi-Asl, Amir Salar

    Annals of medicine and surgery (2012)

    2022  Volume 73, Page(s) 103240

    Abstract: Objective: Breast cancer is the second leading cause of death and the most common cancer among women. 10 to 20 percent of breast cancer samples have a negative triple phenotype that is more metastatic and more difficult to diagnose. Tumor invasion to ... ...

    Abstract Objective: Breast cancer is the second leading cause of death and the most common cancer among women. 10 to 20 percent of breast cancer samples have a negative triple phenotype that is more metastatic and more difficult to diagnose. Tumor invasion to other tissues and the formation of a secondary tumor depend on the epithelial to mesenchymal transition process, and the STAT3 pathway, which is associated with tumor proliferation and invasion and is the target gene for the drug, alantolactone. In this study, the EMT process is evaluated in negative triple-breasted cancer cells treated with alantolactone.
    Methods: We used MDA-MB-231 cell line for assessing the survival rate of triple negative breast cancer cells and MTT test for determining alantolactone dose. We used three doses of 0.01 0.1, and 1 μM of alantolactone for evaluating the cell behavior in cancer invasion pathway. Real-time PCR was used to evaluate the expression of Vimentin, and N-cadherin genes. All of the tests were repeated thrice and the data were analyzed using Prism version 7.0.
    Results: The expression of Vimentin and N-cadherin decreased significantly at 1 μM alantolactone compared to the control group, p < 0.05.
    Conclusion: Alantolactone affects the expression of Vimentin and N-cadherin through STAT3 signaling pathway and suppresses EMT process, metastasis and cancer invasion. This component may be used for treatment of patients with breast cancer.
    Language English
    Publishing date 2022-01-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2745440-X
    ISSN 2049-0801
    ISSN 2049-0801
    DOI 10.1016/j.amsu.2021.103240
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The methylation status of TNF-α and SOCS3 promoters and the regulation of these gene expressions in patients with Behçet's disease.

    Aziz, Shiva Gholizadeh-Ghaleh / Aziz, Sara Gholizadeh-Ghaleh / Khabbazi, Alireza / Alipour, Shahriar

    Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals

    2020  Volume 25, Issue 5, Page(s) 384–390

    Abstract: Introduction: ...

    Abstract Introduction:
    MeSH term(s) Adult ; Behcet Syndrome/genetics ; Behcet Syndrome/pathology ; Biomarkers/metabolism ; Case-Control Studies ; DNA Methylation/genetics ; Female ; Gene Expression Regulation/genetics ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Promoter Regions, Genetic/genetics ; Suppressor of Cytokine Signaling 3 Protein/genetics ; Tumor Necrosis Factor-alpha/genetics
    Chemical Substances Biomarkers ; SOCS3 protein, human ; Suppressor of Cytokine Signaling 3 Protein ; Tumor Necrosis Factor-alpha
    Language English
    Publishing date 2020-06-01
    Publishing country England
    Document type Journal Article
    ZDB-ID 1324372-x
    ISSN 1366-5804 ; 1354-750X
    ISSN (online) 1366-5804
    ISSN 1354-750X
    DOI 10.1080/1354750X.2020.1754912
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Effects of anti-TNF biologic drugs on uveitis severity in Behçet patients: systematic review and Meta-analysis.

    Abolhasani, Somayeh / Khabbazi, Alireza / Hosseini, Foroogh / Gholizadeh-Ghaleh Aziz, Shiva / Alipour, Shahriar

    International journal of ophthalmology

    2022  Volume 15, Issue 5, Page(s) 813–819

    Abstract: Aim: To investigate effects of anti-TNF biologic drugs on uveitis severity (comparing visual acuity logMAR levels) in Behçet patients.: Methods: Three databases PubMed, Scopus, and the Web of Science were searched for qualified papers focusing on the ...

    Abstract Aim: To investigate effects of anti-TNF biologic drugs on uveitis severity (comparing visual acuity logMAR levels) in Behçet patients.
    Methods: Three databases PubMed, Scopus, and the Web of Science were searched for qualified papers focusing on the anti-TNF-α factors treatment in Behçet's disease (BD)-associated uveitis. Studies that were designed pre and post anti-TNF drug treatment, were selected. After determining the search strategy for this study, the relevant data were extracted.
    Results: The initial search was performed in the target databases and a total of about 1458 articles were found. Fifteen articles were selected for systematic review and only 12 of them had inclusion criteria for Meta-analysis (with visual acuity data). The mean dose of prednisolone before and after biological treatments was reported in 5 studies (28.56 and 7.56 mg/kg, respectively). Also, the preliminary results indicate a significant reduction in visual acuity logMAR levels (MD=-1.5 IU/L, 95%CI: -2.1, -0.01).
    Conclusion: Biological drugs significantly reduce the dose of prednisolone and affect visual acuity values.
    Language English
    Publishing date 2022-05-18
    Publishing country China
    Document type Journal Article
    ZDB-ID 2663246-9
    ISSN 2227-4898 ; 2222-3959
    ISSN (online) 2227-4898
    ISSN 2222-3959
    DOI 10.18240/ijo.2022.05.19
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Combination effects of capecitabine, irinotecan and 17-AAG on colorectal cancer cell line (HT-29).

    Zeynali-Moghaddam, Shima / Kheradmand, Fatemeh / Gholizadeh-Ghaleh Aziz, Shiva / Abroon, Sina

    Annals of medicine and surgery (2012)

    2022  Volume 78, Page(s) 103850

    Abstract: Objevtive: Evasion of apoptosis is a major feature of cancer cells, therefore designing treatment strategies to target apoptotic pathways seems effective. In this study, we investigate the effect of 17-AAG (17-allylaminogeldanamycin) alone and in double ...

    Abstract Objevtive: Evasion of apoptosis is a major feature of cancer cells, therefore designing treatment strategies to target apoptotic pathways seems effective. In this study, we investigate the effect of 17-AAG (17-allylaminogeldanamycin) alone and in double and triple combination with capecitabine (Cap) and irinotecan (IR) on HT-29 colon cancer cell line apoptosis.
    Methods: Capase-3, 8, 9, p53 and NF-κB genes expression were analyzed by Real-time PCR. DNA laddering assay was performed to confirm Real-time PCR results.
    Results: Our results showed that all single treatment groups elevated expression of caspase-3, 8, and 9 significantly and IR/Cap was the only double combination group that could upregulate caspase-8 and -9. NF-κB was down-regulated in single treatment and IR/Cap double combination group, significantly. 17-AAG mono-treatment and IR/Cap and Cap/17-AAG double combination group significantly upregulated p53 gene expression.
    Conclusion: Our findings showed proapoptotic effects of 17-AAG alone and in combination with Cap and IR. These findings propose 17-AAG in combination with routine chemotherapy, as a new protocol for colorectal cancer combination therapy.
    Language English
    Publishing date 2022-05-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2745440-X
    ISSN 2049-0801
    ISSN 2049-0801
    DOI 10.1016/j.amsu.2022.103850
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  7. Article ; Online: Alantolactone triggers oxeiptosis in human ovarian cancer cells via Nrf2 signaling pathway.

    Nasirzadeh, Mahdieh / Atari Hajipirloo, Somayeh / Gholizadeh-Ghaleh Aziz, Shiva / Rasmi, Yousef / Babaei, Ghader / Alipour, Shahriar

    Biochemistry and biophysics reports

    2023  Volume 35, Page(s) 101537

    Abstract: Introduction: A growing body of evidence indicated that Alantolactone (ALT) promotes Reactive Oxygen Species (ROS) generation exclusively in cancer cells. Therefore, the aim of this study was to investigate the effect of ALT on the molecular mechanism ... ...

    Abstract Introduction: A growing body of evidence indicated that Alantolactone (ALT) promotes Reactive Oxygen Species (ROS) generation exclusively in cancer cells. Therefore, the aim of this study was to investigate the effect of ALT on the molecular mechanism of oxeiptosis, as a novel cell death pathway due to the high levels of intracellular ROS in ovarian cancer.
    Methods: MTT assay was used to evaluate the effect of ALT on SKOV3 cell viability. mRNA and protein expression levels of Nrf2 (nuclear factor erythroid 2-related factor 2), KEAP1 (Kelch-like ECH-associated protein 1), PGAM5 (phosphoglycerate mutase family member 5), AIFM1 (Mitochondrial Apoptosis-Inducing Factor), Glutathione synthetase (GSS) and glutathione peroxidase (GPX) were analyzed by real time PCR and western blotting methods respectively.
    Results: Our findings showed that ALT inhibits the proliferation of skov3 cells in a time and dose dependent manner and IC50 was 32 μM at 24h.A significant down-regulation of Nrf2, GSH and GPX mRNA levels was seen in skov3 cells incubated with 32 and 64 μM of ALT in comparison with control group, while, mRNA expression levels of PGAM5 and KEAP1 were increased.Western blot analysis showed that ALT significantly decreases protein levels of Nrf2 and increases PGAM5 and KEAP1.ALT dephosphorylated PS116-AIFM1 and total AIFM1 protein level was elevated.
    Conclusion: Our results provided evidence that ALT could be a potential option for ovarian cancer treatment by ROS-mediated oxeiptosis.
    Language English
    Publishing date 2023-09-07
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2831046-9
    ISSN 2405-5808 ; 2405-5808
    ISSN (online) 2405-5808
    ISSN 2405-5808
    DOI 10.1016/j.bbrep.2023.101537
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The role of microRNAs in COVID-19 with a focus on miR-200c.

    Sodagar, Hadi / Alipour, Shahriar / Hassani, Sepideh / Aziz, Shiva Gholizadeh-Ghaleh / Ansari, Mohammad Hasan Khadem / Asghari, Rahim

    Journal of circulating biomarkers

    2022  Volume 11, Page(s) 14–23

    Language English
    Publishing date 2022-03-21
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2802655-X
    ISSN 1849-4544 ; 1849-4544
    ISSN (online) 1849-4544
    ISSN 1849-4544
    DOI 10.33393/jcb.2022.2356
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  9. Article ; Online: Ameliorative effects of tropisetron on liver injury in streptozotocin-induced diabetic rats.

    Gholizadeh-Ghaleh Aziz, Shiva / Naderi, Roya / Mahmodian, Nima

    Archives of physiology and biochemistry

    2019  Volume 127, Issue 4, Page(s) 367–372

    Abstract: This study aimed to evaluate the effect of tropisetron on liver injury induced by diabetes. Thirty-five male Wistar rats were assigned to five groups ( ...

    Abstract This study aimed to evaluate the effect of tropisetron on liver injury induced by diabetes. Thirty-five male Wistar rats were assigned to five groups (
    MeSH term(s) Alanine Transaminase/metabolism ; Animals ; Aspartate Aminotransferases/metabolism ; Blood Glucose/analysis ; Diabetes Complications/etiology ; Diabetes Complications/pathology ; Diabetes Complications/prevention & control ; Diabetes Mellitus, Experimental/complications ; Liver Diseases/etiology ; Liver Diseases/pathology ; Liver Diseases/prevention & control ; Male ; Oxidative Stress/drug effects ; Rats ; Rats, Wistar ; Serotonin 5-HT3 Receptor Antagonists/pharmacology ; Tropisetron/pharmacology
    Chemical Substances Blood Glucose ; Serotonin 5-HT3 Receptor Antagonists ; Tropisetron (6I819NIK1W) ; Aspartate Aminotransferases (EC 2.6.1.1) ; Alanine Transaminase (EC 2.6.1.2)
    Language English
    Publishing date 2019-07-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 1238320-x
    ISSN 1744-4160 ; 1381-3455
    ISSN (online) 1744-4160
    ISSN 1381-3455
    DOI 10.1080/13813455.2019.1640743
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  10. Article ; Online: The human amniotic fluid mesenchymal stem cells therapy on, SKOV3, ovarian cancer cell line.

    Gholizadeh-Ghaleh Aziz, Shiva / Fardyazar, Zahra / Pashaiasl, Maryam

    Molecular genetics & genomic medicine

    2019  Volume 7, Issue 7, Page(s) e00726

    Abstract: Purpose: One of the most common malignancies peculiar to female health with few symptoms, low response to therapy, difficult diagnosis, frequent relapse, and high mortality, is ovarian cancer. Thus, our experiment, using Human amniotic fluid mesenchymal ...

    Abstract Purpose: One of the most common malignancies peculiar to female health with few symptoms, low response to therapy, difficult diagnosis, frequent relapse, and high mortality, is ovarian cancer. Thus, our experiment, using Human amniotic fluid mesenchymal stem cells (hAFMSCs) as a therapeutic tool, aims to find an efficient treatment approach for patients suffering from SKOV3 ovarian cancer.
    Material & methods: In this study, we obtained 5 ml amniotic fluid from 16-20 week pregnant women who underwent amniocentesis for routine prenatal diagnosis by karyotyping in Al-Zahra Hospital of Tabriz University of Medical Sciences, Iran. Using trans wells in 24 wells plate, hAFMSCs were isolated from all samples, co-cultured with SKOV3 ovarian cancer cell line, and characterized via flow cytometry and RT-PCR. Human skin fibroblast cells (HSFCs) were isolated and used as a negative control. SKOV3 and HSFCs' viability after 5 days was evaluated by MTT assay. Cell cycle and apoptotic genes were analyzed by real-time PCR.
    Results: We successfully isolated and characterized hAFMSCs through it positivity for CD44 and CD90 specific mesenchymal stem cell markers and negativity for CD31 and CD45. Oct4 and NANOG were evaluated by RT-PCR as pluripotency markers, and visualized on 2% gel electrophoresis. We established hAFMS cell lines after 5 days of co-culturing the SKOV3 cells, viability was decreased; however, HSFCs did not show toxicity by MTT assay. The genes indicated upregulation and high expression by a real-time PCR.
    Conclusions: Our findings showed that hAFMSCs have natural tumor tropism, and can release soluble factors in a cell culture, which cause an efficient anticancer effect. Thus, we can use hAFMSCs for complete anticancer therapy on SKOV3 cell line at cell culture condition and possibly in vivo in the near future.
    MeSH term(s) Amniotic Fluid/cytology ; Cell Line, Tumor ; Cell Survival ; Coculture Techniques ; Cyclin D1/genetics ; Cyclin D1/metabolism ; Female ; Fibroblasts/cytology ; Fibroblasts/metabolism ; Humans ; Mesenchymal Stem Cells/cytology ; Mesenchymal Stem Cells/metabolism ; Ovarian Neoplasms/metabolism ; Ovarian Neoplasms/pathology ; Pregnancy ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism
    Chemical Substances TP53 protein, human ; Tumor Suppressor Protein p53 ; Cyclin D1 (136601-57-5)
    Language English
    Publishing date 2019-05-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2734884-2
    ISSN 2324-9269 ; 2324-9269
    ISSN (online) 2324-9269
    ISSN 2324-9269
    DOI 10.1002/mgg3.726
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