Ahmed M. Al-Hejin
King Abdulaziz University
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Publication
Featured researches published by Ahmed M. Al-Hejin.
BMC Cancer | 2015
Steve Harakeh; Rania Azar; Esam I. Azhar; Ghazi A. Damanhouri; Mourad Assidi; Muhammad Abu-Elmagd; Mohammed H. Al-Qahtani; Taha Kumosani; Aleksandra Niedzwiecki; M. Rath; Ahmed M. Al-Hejin; Elie K. Barbour; Mona Diab-Assaf
BackgroundAdult T-cell Leukemia (ATL) is a disease with no known cure. The disease manifests itself as an aggressive proliferation of CD4+ cells with the human T-cell Lymphotropic virus type 1 (HTLV-1). The leukemogenesis of the virus is mainly attributed to the viral oncoprotein. Tax activates the Nuclear Factor kappa B (NF-κB) which stimulates the activity and expression of the matrix metalloproteinase-9 (MMP-9). The objective of this study was to investigate the efficacy of a specific nutrient synergy (SNS) on proliferation, Tax expression, NF-κB levels as well as on MMP-9 activity and expression both at the transcriptional and translational levels in two HTLV-1 positive cell lines, HuT-102 and C91-PL at 48h and 96h of incubation. Cytotoxicity of Epigallocatechin-3-gallate (EGCG) was assayed using CytoTox 96 Non-radioactive and proliferation was measured using Cell Titer96TM Nonradioactive Cell Proliferation kit (MTT- based assay). Enzyme linked immunosorbant assay (ELISA) and electrophoretic mobility shift assay (EMSA) were used to assess the effect of SNS on NF-κB mobility. Zymography was used to determine the effects of SNS on the activity and secretion of MMP-9. The expression of MMP-9 was done using RT-PCR at the translational level and Immunoblotting at the transcriptional level.ResultsA significant inhibition of proliferation was seen in both cell lines starting at a concentration of 200μg/ml and in a dose dependent manner. SNS induced a dose dependent decrease in Tax expression, which was paralleled by a down-regulation of the nuclearization of NF-κB. This culminated in the inhibition of the activity of MMP-9 and their expression both at the transcriptional and translational levels.ConclusionsThe results of this study indicate that a specific nutrient synergy targeted multiple levels pertinent to the progression of ATL. Its activity was mediated through the NF-κB pathway, and hence has the potential to be integrated in the treatment of this disease as a natural potent anticancer agent.
Journal of Microbiology and Biotechnology | 2015
Mohammed N. Baeshen; Ahmed M. Al-Hejin; Roop Singh Bora; Mohamed Morsi Ahmed; Hassan A. I. Ramadan; Kulvinder Singh Saini; Nabih A. Baeshen; Elrashdy M. Redwan
Escherichia coli is the most preferred microorganism to express heterologous proteins for therapeutic use, as around 30% of the approved therapeutic proteins are currently being produced using it as a host. Owing to its rapid growth, high yield of the product, cost-effectiveness, and easy scale-up process, E. coli is an expression host of choice in the biotechnology industry for large-scale production of proteins, particularly non-glycosylated proteins, for therapeutic use. The availability of various E. coli expression vectors and strains, relatively easy protein folding mechanisms, and bioprocess technologies, makes it very attractive for industrial applications. However, the codon usage in E. coli and the absence of post-translational modifications, such as glycosylation, phosphorylation, and proteolytic processing, limit its use for the production of slightly complex recombinant biopharmaceuticals. Several new technological advancements in the E. coli expression system to meet the biotechnology industry requirements have been made, such as novel engineered strains, genetically modifying E. coli to possess capability to glycosylate heterologous proteins and express complex proteins, including full-length glycosylated antibodies. This review summarizes the recent advancements that may further expand the use of the E. coli expression system to produce more complex and also glycosylated proteins for therapeutic use in the future.
Frontiers in Cellular and Infection Microbiology | 2015
Haitham A. Yacoub; Ahmed M. Elazzazy; Osama A. Abuzinadah; Ahmed M. Al-Hejin; Maged Mostafa Mahmoud; Steve Harakeh
Host Defense Peptides (HDPs) are small cationic peptides found in several organisms. They play a vital role in innate immunity response and immunomodulatory stimulation. This investigation was designed to study the antimicrobial activities of β-defensin peptide-4 (sAvBD-4) and 10 (sAvBD-4) derived from chickens against pathogenic organisms including bacteria and fungi. Ten bacterial strains and three fungal species were used in investigation. The results showed that the sAvBD-10 displayed a higher bactericidal potency against all the tested bacterial strains than that of sAvBD-4. The exhibited bactericidal activity was significant against almost the different bacterial strains at different peptide concentrations except for that of Pseudomonas aeruginosa (P. aeruginosa) and Streptococcus bovis (Str. bovis) strains where a moderate effect was noted. Both peptides were effective in the inactivation of fungal species tested yielding a killing rate of up to 95%. The results revealed that the synthetic peptides were resistant to salt at a concentration of 50 mM NaCl. However, they lost antimicrobial potency when applied in the presence of high salt concentrations. Based on blood hemolysis studies, a little hemolytic effect was showed in the case of both peptides even when applied at high concentrations. The data obtained from this study indicated that synthetic avian peptides exhibit strong antibacterial and antifungal activity. In conclusion, future work and research should be tailored to a better understanding of the mechanisms of action of those peptides and their potential use in the pharmaceutical industry to help reduce the incidence and impact of infectious agent and be marketed as a naturally occurring antibiotic.
Oncotarget | 2016
Waqas Iqbal; Saleh Al-Karim; Ahmed M. Al-Hejin; Hasan Mukhtar; Kulvinder Singh Saini
Tumor comprises of heterogeneous population of cells where not all the disseminated cancer cells have the prerogative and “in-build genetic cues” to form secondary tumors. Cells with stem like properties complemented by key signaling molecules clearly have shown to exhibit selective growth advantage to form tumors at distant metastatic sites. Thus, defining the role of cancer stem cells (CSC) in tumorigenesis and metastasis is emerging as a major thrust area for therapeutic intervention. Precise relationship and regulatory mechanisms operating in various signal transduction pathways during cancer dissemination, extravasation and angiogenesis still remain largely enigmatic. How the crosstalk amongst circulating tumor cells (CTC), epithelial mesenchymal transition (EMT) process and CSC is coordinated for initiating the metastasis at secondary tissues, and during cancer relapse could be of great therapeutic interest. The signal transduction mechanisms facilitating the dissemination, infiltration of CSC into blood stream, extravasations, progression of metastasis phenotype and angiogenesis, at distant organs, are the key pathologically important vulnerabilities being elucidated. Therefore, current new drug discovery focus has shifted towards finding “key driver genes” operating in parallel signaling pathways, during quiescence, survival and maintenance of stemness in CSC. Understanding these mechanisms could open new horizons for tackling the issue of cancer recurrence and metastasis-the cause of ~90% cancer associated mortality. To design futuristic & targeted therapies, we propose a multi-pronged strategy involving small molecules, RNA interference, vaccines, antibodies and other biotechnological modalities against CSC and the metastatic signal transduction cascade.
Journal of Bioremediation and Biodegradation | 2014
Ebtesam El Bestawy; Ahmed M. Al-Hejin; Ranya Amer; Rzaz Abdulrazaq Kashmeri
The study aimed to investigate the ability of indigenous and/or exogenous free living bacteria either individual or as mixed culture to decontaminate raw domestic wastewater. Seven indigenous and two exogenous bacteria were selected and identified using traditional as well as molecular characterization, then used in the batch remediation system for seven days. Results indicated that the raw wastewater was relatively of high strength according to the levels of all the tested parameters. Treatment efficiency was time and bacterial species dependent. In general, the mixture of the tested bacteria considered the most efficient for the removal of all the tested parameters. Pseudomonas stutzeri (PS) was perfect for removing organic matter (BOD and COD) while the mixed culture considered the most efficient for removing fecal coliform (≈100%) brought them to safe (60, 100 mg/l and ≈ 0.0 CFU/ml respectively) discharge limits (MPL) stated by the Egyptian and Saudi Environmental laws that regulate discharging of domestic and industrial wastewater into fresh and saline open water. In addition, high removal efficiencies of TSS, FOG and TC recording 39.1, 90.0 and 99.0% respectively were achieved by B. amyloliquefaciens (S1), E. coli (Rz6) and the mixed culture respectively. However, their residuals still higher (23.3, 20 and 200 fold respectively) than their MPLs for the safe discharge due to the short treatment course. Therefore, longer treatment time and/or using biofilm of the selected bacteria are highly recommended to bring the contaminated domestic effluent it to the safe limits for the environment. The present study confirmed the ability of the selected bacteria for the removal of the target contaminants especially pathogenic bacteria (coliform) and thus can be manipulated efficiently to decontaminate polluted systems providing the optimum degradation conditions.
Biotechnology & Biotechnological Equipment | 2016
Raziuddin Khan; Mohammed N. Baeshen; Kulvinder Singh Saini; Roop Singh Bora; Ahmed M. Al-Hejin; Nabih A. Baeshen
ABSTRACT Bacterial resistance to antibiotics, first a major concern in the 1960s, has re-emerged worldwide over the last 20 years. The World Health Organization (WHO) and other health organizations have, therefore, declared ‘war’ against human microbial pathogens, particularly hospital-acquired infections, and have made drug discovery a top priority for these diseases. Because these bacteria are refractory to conventional chemotherapy, medicinal and herbal plants used in various countries should be assessed for their therapeutic potential; these valuable bio-resources are a reservoir of complex bioactive molecules. Earlier studies from our laboratory on Rhazya stricta, a native herbal shrub of Asia, have shown that this plant has a number of therapeutic properties. In this study, we evaluated the antimicrobial activities of various concentrations of five solvent extracts (aqueous alkaloid, aqueous non-alkaloid, organic alkaloid, organic non-alkaloid and whole aqueous extracts) derived from R. stricta leaves against several multidrug-resistant, human-pathogenic bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and extended-spectrum beta-lactamase-positive Escherichia coli. In vitro, molecular and electron microscopy analyses conclusively demonstrated the antimicrobial effects of these extracts against a panel of Gram-negative and Gram-positive bacteria. The organic alkaloid extract was the most effective against E. coli and MRSA, resulting in cell membrane disruption visible with transmission electron microscopy. In the near future, we intend to further focus and delineate the molecular mechanism-of-action for specific alkaloids of R. stricta, particularly against MRSA.
International Journal of Oncology | 2014
Steve Harakeh; Raefa Abou-khouzam; Ghazi A. Damanhouri; Ahmed M. Al-Hejin; Taha Kumosani; Aleksandra Niedzwiecki; M. Rath; Elie K. Barbour; Mona Diab-Assaf; Rania Azar
Experimental and clinical studies have revealed the effectiveness of a specific nutrient synergy (SNS) mixture composed of ascorbic acid (AA), lysine, proline, arginine, epigallocatechin gallate (EGCG) and other micronutrients in targeting crucial physiological mechanisms involved in cancer progression and metastasis. HTLV-1 causes adult T-cell leukemia (ATL). The spread and metastases of ATL as well as other tumors has been associated with matrix metalloproteinases, especially the gelatinases MMP-2 and MMP-9. The objective of this study was to investigate whether SNS, AA and EGCG affects the gelatinolytic activity of MMP-2 and its transcriptional and translational levels in HTLV-1-positive and -negative malignant T-cells. The results indicated that SNS and EGCG caused a dose-dependent decline in the activity, transcription and translation of MMP-2 after treatment with SNS and EGCG, while AA was only able to inhibit the activity at maximum doses tested and to some extent, the protein expression levels of MMP-2, without affecting their transcriptional levels. The highest activity was noted in the case of SNS which is likely to be due to a synergistic effect of the different constituents in the formulation. These results point towards the potential integration of SNS in the anti-invasive treatment of ATL and related diseases.
Molecules | 2018
Elrashdy M. Redwan; Ahmed M. Al-Hejin; Hussein A. Almehdar; Abdelrahman Elsaway; Vladimir N. Uversky
Butyrophilins (BTNs) are a group of the moonlighting proteins, some members of which are secreted in milk. They constitute a large family of structurally similar type 1 transmembrane proteins from the immunoglobulin superfamily. Although the founding member of this family is related to lactation, participating in the secretion, formation and stabilization of milk fat globules, it may also have a cell surface receptor function. Generally, the BTN family members are known to modulate co-stimulatory responses, T cell selection, differentiation, and cell fate determination. Polymorphism of these genes was shown to be associated with the pathology of several human diseases. Despite their biological significance, structural information on human butyrophilins is rather limited. Based on their remarkable multifunctionality, butyrophilins seem to belong to the category of moonlighting proteins, which are known to contain intrinsically disordered protein regions (IDPRs). However, the disorder status of human BTNs was not systematically investigated as of yet. The goal of this study is to fill this gap and to evaluate peculiarities of intrinsic disorder predisposition of the members of human BTN family, and to find if they have IDPRs that can be attributed to the multifunctionality of these important proteins.
Human antibodies | 2017
Fatimah M. Alshanqiti; Saad B. Almasaudi; Ahmed M. Al-Hejin; Elrashdy M. Redwan
Its known that diphtheria and tetanus are a contagious lethal diseases over the years, they caused by pathogenic microbes corynebacterium diphtheria and Clostridium tetani, respectively. The diseases result from the production of bacterial toxin. Vaccination with bacterial toxoid vaccines adsorbed on particulates adjuvants still are the best way to prevent this epidemic diseases from spread. The particulate vaccines have been shown to be more efficient than soluble one for the induction of the immune responses. Nanoparticles can be engineered to enhance the immune responses. As well known the immune response to inactivate killed and subunit vaccine enhances by alum adjuvants. The adjuvants examined and tested after reducing its size to particle size, thus mimic size of viruses which is considered smallest units can derive the immune system. The major issue is minimizing the adjuvant particles, to gain insight of resulting immunity types and impact on immune response. The adjuvant effect of micro/nanoparticles appears to largely be a consequence of their uptake into antigen presenting cells.
Biosciences, Biotechnology Research Asia | 2017
Afnan Abdul-Jalil Farhan; Munazza Gull; Sawsan Abdulaziz Rahimuddin; Taha Kumosani; Ahmed M. Al-Hejin; Abida Kausar; Muhammad Aamer Mehmood
1Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia. 2Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia. 3Department of Botany, Faculty of Science, Govt: College University (Women) Faisalabad, Pakistan. 4Department of Bioinformatics & Biotechnology, Government College University Faisalabad, 38000, Pakistan.