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Ahmed Ashour

Researcher at Mansoura University

Publications -  74
Citations -  987

Ahmed Ashour is an academic researcher from Mansoura University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 15, co-authored 46 publications receiving 624 citations. Previous affiliations of Ahmed Ashour include University of Alabama & University of Texas MD Anderson Cancer Center.

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Targeting elongation factor-2 kinase (eEF-2K) induces apoptosis in human pancreatic cancer cells.

TL;DR: It is shown, for the first time, that the down-regulation of eEF-2K leads to induction of intrinsic, extrinsic as well as AIF-dependent apoptosis in PaCa cells, suggesting that eEF -2K may represent an attractive therapeutic target for the future anticancer agents in Pa Ca.
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FOXM1 regulates expression of eukaryotic elongation factor 2 kinase and promotes proliferation, invasion and tumorgenesis of human triple negative breast cancer cells.

TL;DR: This study provides the first evidence about the transcriptional regulation of eEF2K in TNBC and the role ofFOXM1 in mediating breast cancer cell proliferation, survival, migration/invasion, progression and tumorgenesis and highlighting the potential of FOXM1/e EF2K axis as a molecular target in breast and other cancers.
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Calendulaglycoside A Showing Potential Activity Against SARS-CoV-2 Main Protease: Molecular Docking, Molecular Dynamics, and SAR Studies.

TL;DR: A promising SAR is clarified responsible for the antiviral activity against the SARS-CoV-2 Mpro and the design of new drug candidates targeting it as well is clarified and could be promising for fast examining the previously isolated triterpenes both pre-clinically and clinically for the treatment of COVID-19.
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Elongation factor‐2 kinase regulates TG2/β1 integrin/Src/uPAR pathway and epithelial–mesenchymal transition mediating pancreatic cancer cells invasion

TL;DR: Results show, for the first time, that eEF‐2K is involved in regulation of the invasive phenotype of PaCa cells through promoting a new signalling pathway, which is mediated by TG2/β1 integrin/Src/uPAR/MMP‐2, and the induction of EMT biomarkers which enhance cancer cell motility and metastatic potential.
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Molecular docking reveals the potential of: Cleome amblyocarpa isolated compounds to inhibit COVID-19 virus main protease

TL;DR: The explanation of the SAR required for targeting the newly emerged SARS-CoV-2 protease is explained and facilitates the future design and synthesis of new drugs targeting it as well.