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  1. Article ; Online: Hypermethylated miR-424 in Colorectal Cancer Subsequently Upregulates VEGF.

    Ghonbalani, Zahra Nouri / Shahmohamadnejad, Shiva / Pasalar, Parvin / Khalili, Ehsan

    Journal of gastrointestinal cancer

    2021  Volume 53, Issue 2, Page(s) 380–386

    Abstract: Purpose: Colorectal cancer (CRC) is the second leading cause of death from cancer in adults. Recent advances have shown that cancer cells can have some epigenetic changes involved in all stages of cancer. It has also been shown that miR-424 acts as gene ...

    Abstract Purpose: Colorectal cancer (CRC) is the second leading cause of death from cancer in adults. Recent advances have shown that cancer cells can have some epigenetic changes involved in all stages of cancer. It has also been shown that miR-424 acts as gene expression regulators in many biological processes, including angiogenesis with mediators such as VEGF. In the current study, to identify the potential role of miR-424 in colorectal cancer progression, methylation status of miR-424 promoter region and its expression level have been evaluated. Besides, the correlation between VEGF level and miR-424 expression level has been assessed.
    Methods: Methylation status miR-424 promoter was assessed using methylation-specific polymerase chain reaction (MSP). The expression level of miR-424 in human colorectal cancer tissue was analyzed by quantitative PCR. HCT116 cell line was selected to evaluate the correlation between the miR-424 expression level and the promoter's methylation status. VEGF expression, one out of mir-424 targets involved in angiogenesis and cancer progression, was measured by western blot analysis in the pairs of cancer tissues and their adjacent tissues.
    Results: Our results have revealed that the promoter region of miR-424 is methylated in cancer cells compared to normal cells, leading to downregulation of miR-424 in the colorectal cancer tissues compared to the normal tissues. Also, we found that the expression protein's level of VEGF in the tumor cells is increased compared with normal tissues.
    Conclusion: The present study suggests that hypermethylation downregulates miR-424. VEGF expression is upregulated with decreased miR-424 in colorectal cancer, which results in cancer progression.
    MeSH term(s) Cell Line, Tumor ; Colorectal Neoplasms/pathology ; DNA Methylation ; Gene Expression Regulation, Neoplastic ; Humans ; MicroRNAs/metabolism ; Neovascularization, Pathologic/genetics ; Vascular Endothelial Growth Factor A/genetics ; Vascular Endothelial Growth Factor A/metabolism
    Chemical Substances MIRN424 microrna, human ; MicroRNAs ; VEGFA protein, human ; Vascular Endothelial Growth Factor A
    Language English
    Publishing date 2021-03-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2452514-5
    ISSN 1941-6636 ; 1559-0739 ; 1941-6628 ; 1537-3649
    ISSN (online) 1941-6636 ; 1559-0739
    ISSN 1941-6628 ; 1537-3649
    DOI 10.1007/s12029-021-00614-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Recent Advances in siRNA Delivery Systems for Prostate Cancer Therapy.

    Aghamiri, Shahin / Raee, Pourya / Shahmohamadnejad, Shiva / Shabani, Sasan / Ghorbani, Jaber / Sameni, Marzieh / Ebrahimi, Mohammad Taha

    Current pharmaceutical biotechnology

    2021  Volume 23, Issue 4, Page(s) 579–593

    Abstract: The critical problems of conventional prostate cancer therapeutic strategies like nonspecific toxicity and multi-drug resistance prompted the development and application of countless nanoparticle- based siRNA therapeutics. Unfortunately, siRNA-based ... ...

    Abstract The critical problems of conventional prostate cancer therapeutic strategies like nonspecific toxicity and multi-drug resistance prompted the development and application of countless nanoparticle- based siRNA therapeutics. Unfortunately, siRNA-based therapeutics suffer from the lack of safe and effective delivery systems, immune system stimulation, poor knowledge of nano-bio interactions, and limitations concerning designing, manufacturing, clinical translation, and commercialization. In this review, we provide cutting-edge advances in nanoparticle-mediated siRNA delivery carriers like polymeric systems, lipid systems, specific systems, and rigid nanoparticles for the treatment of prostate cancer. Moreover, co-delivery of conventional chemotherapy drugs with siRNA as a revolutionary robust strategy for prostate cancer combinational therapy is completely covered.
    MeSH term(s) Drug Delivery Systems ; Humans ; Lipids ; Male ; Nanoparticles ; Neoplasms ; Prostatic Neoplasms/genetics ; Prostatic Neoplasms/therapy ; RNA, Small Interfering/genetics
    Chemical Substances Lipids ; RNA, Small Interfering
    Language English
    Publishing date 2021-06-15
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2132197-8
    ISSN 1873-4316 ; 1389-2010
    ISSN (online) 1873-4316
    ISSN 1389-2010
    DOI 10.2174/1389201022666210615123211
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: May we target double-membrane vesicles and oxysterol-binding protein to combat SARS-CoV-2 infection?

    Shahmohamadnejad, Shiva / Nabavi, Seyed Fazel / Habtemariam, Solomon / Sarkar, Kasturi / Sil, Parames C / Dowran, Razieh / Nabavi, Seyed Mohammad

    Cell biology international

    2020  Volume 44, Issue 9, Page(s) 1770–1772

    MeSH term(s) Betacoronavirus/metabolism ; COVID-19 ; Cell Membrane/drug effects ; Cell Membrane/metabolism ; Coronavirus Infections/drug therapy ; Coronavirus Infections/metabolism ; Cytochrome P-450 CYP3A Inhibitors/administration & dosage ; Cytochrome P-450 CYP3A Inhibitors/metabolism ; Drug Delivery Systems/methods ; Humans ; Itraconazole/administration & dosage ; Itraconazole/metabolism ; Nocodazole/administration & dosage ; Nocodazole/metabolism ; Pandemics ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/metabolism ; Receptors, Steroid/antagonists & inhibitors ; Receptors, Steroid/metabolism ; SARS-CoV-2 ; Tubulin Modulators/administration & dosage ; Tubulin Modulators/metabolism
    Chemical Substances Cytochrome P-450 CYP3A Inhibitors ; Receptors, Steroid ; Tubulin Modulators ; oxysterol binding protein ; Itraconazole (304NUG5GF4) ; Nocodazole (SH1WY3R615)
    Keywords covid19
    Language English
    Publishing date 2020-06-23
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1143453-3
    ISSN 1095-8355 ; 1065-6995
    ISSN (online) 1095-8355
    ISSN 1065-6995
    DOI 10.1002/cbin.11400
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Aberrant methylation of miR-124 upregulates DNMT3B in colorectal cancer to accelerate invasion and migration.

    Shahmohamadnejad, Shiva / Nouri Ghonbalani, Zahra / Tahbazlahafi, Behnoosh / Panahi, Ghodratollah / Meshkani, Reza / Emami Razavi, Amirnader / Shokri Afra, Hajar / Khalili, Ehsan

    Archives of physiology and biochemistry

    2020  Volume 128, Issue 6, Page(s) 1503–1509

    Abstract: The dysregulation of microRNA expression is significantly associated with the initiation and development of CRC. miR-124 is markedly downregulated in colorectal cancer. In the present study, the effects of methylation, over expression and downregulation ... ...

    Abstract The dysregulation of microRNA expression is significantly associated with the initiation and development of CRC. miR-124 is markedly downregulated in colorectal cancer. In the present study, the effects of methylation, over expression and downregulation of miR-124 and its target gene DNMT3B on the proliferation, migration and invasion of colorectal cell line were investigated. The promoter methylation status of miR-124 in the CRC was investigated by methylation specific PCR (MSP). The potential role of miR-124 expression in CRC cells was investigated using the demethylation reagent 5-Aza-CdR and transfection of miR-124 mimic/antimir. MSP revealed that miR-124 promoter region was hypermethylated, result in its significant downregulation in tumour tissues. We showed miR-124 expression was upregulated following 5-AZA-CdR treatment. Transfected Hct-116 cell line with miR-124 leads to decreased DNMT3B expression, cell proliferation, migration and invasion of HCT-116. In conclusion, our data indicate that miR-124 suppress colorectal cancer proliferation, migration and invasion through downregulating DNMT3B level.
    MeSH term(s) Humans ; Methylation ; Gene Expression Regulation, Neoplastic ; Cell Movement/genetics ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/pathology ; Cell Line, Tumor ; MicroRNAs/genetics ; MicroRNAs/metabolism
    Chemical Substances MicroRNAs ; MIRN124 microRNA, human
    Language English
    Publishing date 2020-06-18
    Publishing country England
    Document type Journal Article
    ZDB-ID 1238320-x
    ISSN 1744-4160 ; 1381-3455
    ISSN (online) 1744-4160
    ISSN 1381-3455
    DOI 10.1080/13813455.2020.1779311
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Therapeutic Attributes of Endocannabinoid System against Neuro-Inflammatory Autoimmune Disorders.

    Ahmed, Ishtiaq / Rehman, Saif Ur / Shahmohamadnejad, Shiva / Zia, Muhammad Anjum / Ahmad, Muhammad / Saeed, Muhammad Muzammal / Akram, Zain / Iqbal, Hafiz M N / Liu, Qingyou

    Molecules (Basel, Switzerland)

    2021  Volume 26, Issue 11

    Abstract: In humans, various sites like cannabinoid receptors (CBR) having a binding affinity with cannabinoids are distributed on the surface of different cell types, where endocannabinoids (ECs) and derivatives of fatty acid can bind. The binding of these ... ...

    Abstract In humans, various sites like cannabinoid receptors (CBR) having a binding affinity with cannabinoids are distributed on the surface of different cell types, where endocannabinoids (ECs) and derivatives of fatty acid can bind. The binding of these substance(s) triggers the activation of specific receptors required for various physiological functions, including pain sensation, memory, and appetite. The ECs and CBR perform multiple functions via the cannabinoid receptor 1 (CB
    MeSH term(s) Animals ; Autoimmune Diseases of the Nervous System/drug therapy ; Autoimmune Diseases of the Nervous System/metabolism ; Cytokines/metabolism ; Endocannabinoids/metabolism ; Endocannabinoids/pharmacology ; Endocannabinoids/therapeutic use ; Humans ; Immunosuppressive Agents/pharmacology ; Immunosuppressive Agents/therapeutic use ; Leukocytes/metabolism ; Receptors, Cannabinoid/drug effects ; Receptors, Cannabinoid/metabolism ; T-Lymphocytes/metabolism
    Chemical Substances Cytokines ; Endocannabinoids ; Immunosuppressive Agents ; Receptors, Cannabinoid
    Language English
    Publishing date 2021-06-03
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules26113389
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: May we target double-membrane vesicles and oxysterol-binding protein to combat SARS-CoV-2 infection?

    Shahmohamadnejad, Shiva / Nabavi, Seyed Fazel / Habtemariam, Solomon / Sarkar, Kasturi / Sil, Parames C / Dowran, Razieh / Nabavi, Seyed Mohammad

    Cell Biol Int

    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #361193
    Database COVID19

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  7. Article ; Online: May we target double‐membrane vesicles and oxysterol‐binding protein to combat SARS‐CoV‐2 infection?

    Shahmohamadnejad, Shiva / Nabavi, Seyed Fazel / Habtemariam, Solomon / Sarkar, Kasturi / Sil, Parames C. / Dowran, Razieh / Nabavi, Seyed Mohammad

    Cell Biology International

    2020  Volume 44, Issue 9, Page(s) 1770–1772

    Keywords Cell Biology ; General Medicine ; covid19
    Language English
    Publisher Wiley
    Publishing country us
    Document type Article ; Online
    ZDB-ID 1143453-3
    ISSN 1095-8355 ; 1065-6995
    ISSN (online) 1095-8355
    ISSN 1065-6995
    DOI 10.1002/cbin.11400
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Hesperetin is a potent bioactivator that activates SIRT1-AMPK signaling pathway in HepG2 cells.

    Shokri Afra, Hajar / Zangooei, Mohammad / Meshkani, Reza / Ghahremani, Mohammad Hossein / Ilbeigi, Davod / Khedri, Azam / Shahmohamadnejad, Shiva / Khaghani, Shahnaz / Nourbakhsh, Mitra

    Journal of physiology and biochemistry

    2019  Volume 75, Issue 2, Page(s) 125–133

    Abstract: Sirtuin 1 (SIRT1) is a deacetylase enzyme that plays crucial roles in controlling many cellular processes and its downregulation has been implicated in different metabolic disorders. Recently, several polyphenols have been considered as the effective ... ...

    Abstract Sirtuin 1 (SIRT1) is a deacetylase enzyme that plays crucial roles in controlling many cellular processes and its downregulation has been implicated in different metabolic disorders. Recently, several polyphenols have been considered as the effective therapeutic approaches that appear to influence SIRT1. The main goal of this study was to evaluate the effect of hesperetin, a citrus polyphenolic flavonoid, on SIRT1 and AMP-activated kinase (AMPK). HepG2 cells were treated with hesperetin in the presence or absence of EX-527, a SIRT1 specific inhibitor, for 24 h. Resveratrol was used as a positive control. SIRT1 gene expression, protein level, and activity were measured by RT-PCR, Western blotting, and fluorometric assay, respectively. AMPK phosphorylation was also determined by Western blotting. Our results indicated a significant increase in SIRT1 protein level and activity as well as an induction of AMPK phosphorylation by hesperetin. These effects of hesperetin were abolished by EX-527. Furthermore, hesperetin reversed the EX-527 inhibitory effects on SIRT1 protein expression and AMPK phosphorylation. These findings suggest that hesperetin can be a novel SIRT1 activator, even stronger than resveratrol. Therefore, the current study may introduce hesperetin as a new strategy aimed at upregulation SIRT1-AMPK pathway resulting in various cellular processes regulation.
    MeSH term(s) AMP-Activated Protein Kinases/metabolism ; Carbazoles/pharmacology ; Hep G2 Cells ; Hesperidin/pharmacology ; Humans ; Phosphorylation/drug effects ; Resveratrol/pharmacology ; Signal Transduction/drug effects ; Sirtuin 1/antagonists & inhibitors ; Sirtuin 1/metabolism
    Chemical Substances 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide ; Carbazoles ; Hesperidin (E750O06Y6O) ; AMP-Activated Protein Kinases (EC 2.7.11.31) ; SIRT1 protein, human (EC 3.5.1.-) ; Sirtuin 1 (EC 3.5.1.-) ; Resveratrol (Q369O8926L) ; hesperetin (Q9Q3D557F1)
    Language English
    Publishing date 2019-05-15
    Publishing country Spain
    Document type Journal Article
    ZDB-ID 1325104-1
    ISSN 1877-8755 ; 0034-9402 ; 1138-7548
    ISSN (online) 1877-8755
    ISSN 0034-9402 ; 1138-7548
    DOI 10.1007/s13105-019-00678-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Various interferon (IFN)-inducible transmembrane (IFITM) proteins for COVID-19, is there a role for the combination of mycophenolic acid and interferon?

    Dowran, Razieh / Nabavi, Seyed Fazel / Habtemariam, Solomon / Banach, Maciej / Shahmohamadnejad, Shiva / Cismaru, Cosmin Andrei / Berindan-Neagoe, Ioana / Sahebnasagh, Adeleh / Nabavi, Seyed Mohammad

    Biochimie

    2020  Volume 177, Page(s) 50–52

    Abstract: Various interferon (IFN)-inducible transmembrane (IFITM) proteins are known to be expressed in human tissues though only IFITM 1-3 are inducible by IFN. Numerous studies have shown that activation of IFITM3 could suppress infection by influenza and ... ...

    Abstract Various interferon (IFN)-inducible transmembrane (IFITM) proteins are known to be expressed in human tissues though only IFITM 1-3 are inducible by IFN. Numerous studies have shown that activation of IFITM3 could suppress infection by influenza and coronaviruses such as the Middle East Respiratory Syndrome Coronavirus (MERS-CoV). In view of the potential application of IFITM proteins' induction to target SARS-CoV-2 infection that causes COVID-19, this article layout insights into the known antiviral mechanisms and therapeutic agents related to IFITM. Blocking viral entry through various mechanisms and the potential application of the FDA approved immunosuppressant agent, mycophenolic acid, as inducer of IFITM3 are among those discussed.
    MeSH term(s) Animals ; Betacoronavirus/drug effects ; COVID-19 ; Coronavirus Infections/drug therapy ; Coronavirus Infections/immunology ; Coronavirus Infections/metabolism ; Humans ; Immunosuppressive Agents/pharmacology ; Interferons/pharmacology ; Membrane Proteins/drug effects ; Membrane Proteins/immunology ; Mycophenolic Acid/pharmacology ; Pandemics ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/immunology ; Pneumonia, Viral/metabolism ; RNA-Binding Proteins/drug effects ; RNA-Binding Proteins/immunology ; SARS-CoV-2
    Chemical Substances IFITM3 protein, human ; Immunosuppressive Agents ; Membrane Proteins ; RNA-Binding Proteins ; Interferons (9008-11-1) ; Mycophenolic Acid (HU9DX48N0T)
    Keywords covid19
    Language English
    Publishing date 2020-08-14
    Publishing country France
    Document type Journal Article
    ZDB-ID 120345-9
    ISSN 1638-6183 ; 0300-9084
    ISSN (online) 1638-6183
    ISSN 0300-9084
    DOI 10.1016/j.biochi.2020.08.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Therapeutic Attributes of Endocannabinoid System against Neuro-Inflammatory Autoimmune Disorders

    Ishtiaq Ahmed / Saif Ur Rehman / Shiva Shahmohamadnejad / Muhammad Anjum Zia / Muhammad Ahmad / Muhammad Muzammal Saeed / Zain Akram / Hafiz M. N. Iqbal / Qingyou Liu

    Molecules, Vol 26, Iss 3389, p

    2021  Volume 3389

    Abstract: In humans, various sites like cannabinoid receptors (CBR) having a binding affinity with cannabinoids are distributed on the surface of different cell types, where endocannabinoids (ECs) and derivatives of fatty acid can bind. The binding of these ... ...

    Abstract In humans, various sites like cannabinoid receptors (CBR) having a binding affinity with cannabinoids are distributed on the surface of different cell types, where endocannabinoids (ECs) and derivatives of fatty acid can bind. The binding of these substance(s) triggers the activation of specific receptors required for various physiological functions, including pain sensation, memory, and appetite. The ECs and CBR perform multiple functions via the cannabinoid receptor 1 (CB 1 ); cannabinoid receptor 2 (CB 2 ), having a key effect in restraining neurotransmitters and the arrangement of cytokines. The role of cannabinoids in the immune system is illustrated because of their immunosuppressive characteristics. These characteristics include inhibition of leucocyte proliferation, T cells apoptosis, and induction of macrophages along with reduced pro-inflammatory cytokines secretion. The review seeks to discuss the functional relationship between the endocannabinoid system (ECS) and anti-tumor characteristics of cannabinoids in various cancers. The therapeutic potential of cannabinoids for cancer—both in vivo and in vitro clinical trials—has also been highlighted and reported to be effective in mice models in arthritis for the inflammation reduction, neuropathic pain, positive effect in multiple sclerosis and type-1 diabetes mellitus, and found beneficial for treating in various cancers. In human models, such studies are limited; thereby, further research is indispensable in this field to get a conclusive outcome. Therefore, in autoimmune disorders, therapeutic cannabinoids can serve as promising immunosuppressive and anti-fibrotic agents.
    Keywords endocannabinoid system ; CB 1 and CB 2 receptors ; cannabis ; cancer ; immunosuppressive ; Organic chemistry ; QD241-441
    Subject code 610
    Language English
    Publishing date 2021-06-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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