Anthony McElligott
Assistant Professor in Molecular Haematology
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About
Dr. Anthony McElligott is an Assistant Professor in Molecular Haematology at Trinity College Dublin, Ireland. His research focuses on the synthesis and biochemical evaluation of compounds for their antiproliferative and pro-apoptotic effects in chronic lymphocytic leukemia and other hematological malignancies. Recent publications include studies on the epidemiology of chronic lymphocytic leukemia and the exploration of novel anti-cancer mechanisms involving diaryl guanidinium derivatives.
Articles (5)
Year:
2024
Chronic lymphocytic leukaemia (CLL) is a malignancy of the immune B lymphocyte cells and is the most common leukaemia diagnosed in developed countries. In this paper, we report the synthesis and antiproliferative effects of a series of (E)-9-(2-nitrovinyl)anthracenes and related nitrostyrene compounds in CLL cell lines and also in Burkitt’s lymphoma (BL) cell lines, a rare form of non-Hodgkin’s immune B-cell lymphoma. The nitrostyrene scaffold was identified as a lead structure for the development of effective compounds targeting BL and CLL. The series of structurally diverse nitrostyrenes was synthesised via Henry–Knoevenagel condensation reactions. Single-crystal X-ray analysis confirmed the structure of (E)-9-chloro-10-(2-nitrobut-1-en-1-yl)anthracene (19f) and the related 4-(anthracen-9-yl)-1H-1,2,3-triazole (30a). The (E)-9-(2-nitrovinyl)anthracenes 19a, 19g and 19i–19m were found to elicit potent antiproliferative effects in both BL cell lines EBV−MUTU-1 (chemosensitive) and EBV+ DG-75 (chemoresistant) with >90% inhibition at 10 μM. Selected (E)-9-(2-nitrovinyl)anthracenes demonstrated potent antiproliferative activity in CLL cell lines, with IC50 values of 0.17 μM (HG-3) and 1.3 μM (PGA-1) for compound 19g. The pro-apoptotic effects of the most potent compounds 19a, 19g, 19i, 19l and 19m were demonstrated in both CLL cell lines HG-3 and PGA-1. The (E)-nitrostyrene and (E)-9-(2-nitrovinyl)anthracene series of compounds offer potential for further development as novel chemotherapeutics for CLL.
Year:
2023
Year:
2022
Year:
2021
Year:
2020
Collaborators (4)
Darren Fayne
Trinity College Dublin
Mary J. Meegan
Trinity College Dublin
Isabel Rozas
Trinity College Dublin
Maria Jose Santos-Martinez
Assistant Professor (Ussher)
Trinity College Dublin Faculty of Health Sciences
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