Hafsa Abbas's research while affiliated with The University of Warwick and other places

Publications (4)

Article
Full-text available
Background Tumor glycolysis is a target for cancer chemotherapy. Methylglyoxal (MG) is a reactive metabolite formed mainly as a by-product in anaerobic glycolysis, metabolized by glyoxalase 1 (Glo1) of the glyoxalase system. We investigated the role of MG and Glo1 in cancer chemotherapy related in multidrug resistance (MDR). Methods Human Glo1 was...
Article
Full-text available
The global pandemic of COVID-19 disease caused by infection with the SARS-CoV-2 coronavirus, has produced an urgent requirement and search for improved treatments while effective vaccines are developed. A strategy for improved drug therapy is to increase levels of endogenous reactive metabolites for selective toxicity to SARS-CoV-2 by preferential...
Preprint
There is an urgent requirement for improved treatments of COVID-19 disease. A strategy for chemotherapy is to increase levels of endogenous reactive metabolites — such as reactive oxygen species and arginine-directed glycating agent, methylglyoxal — for selective toxicity to SARS-CoV-2. Sequence analysis of functional domains in the SARS-CoV-2 prot...

Citations

... The lead compound is a cell-permeable prodrug diester of the Glo1 inhibitor, S-p-bromobenzylglutathione cyclopentyl diester (BBGD) [28]. BBGD antitumor activity was enhanced 60-fold in hypoxia, where increased anerobic glycolysis is associated with the increased formation of MG [29,30]. An increase in cellular MG to cytotoxic levels was also involved in the mechanism of action of multiple classes of clinical antitumor drugs: DNA alkylators-mechlorethamine and mitomycin C; topoisomerase inhibitorscamptothecin, doxorubicin, and etoposide; antitubulins-paclitaxel and vincristine; and an antimetabolite, methotrexate. ...
... To accomplish this task, the SARS-CoV-2 virus exploits arginine, a unique amino with side chains capable of piercing cell membranes [103,104]. For example, the S antigen of the SARS-CoV-2 virus contains a polybasic cleavage motif, "Proline-Arginine-Arginine-Alanine (PRRA)", in which the bi-arginine forms a pore in the cell membrane, initiating fusion [105]. Aside from utilizing arginine, the SARS-CoV-2 virus also activates HERVs, providing additional fusogens-a "plan B"-for ensuring viral entry [34]. ...
... Honey may inhibit SARS-CoV2 proteases as some compounds of honey may be able to bind SARSCoV-2 protease 197 . Methylglyoxal (MGO) modification might be involved in SARS-CoV-2 replication 198 . MGO is a component of manuka honey that can inhibit enveloped virus growth, viral transcription, and translation 199 . ...
... The U.S. Food and Drug Administration (FDA) recently revoked its Emergency Use Authorization (EUA) to treat COVID-19 [187]. Other drugs include the anti-HIV drugs Lopinavir-Ritonavir in combination with Ribavirin [188][189][190], tumor chemotherapy drugs, doxorubicin and paclitaxel [191], traditional herbal medicines [192], broad spectrum antiviral drug Niclosamide [193], Janus-associated kinase (JAK) 1 and 2 inhibitor, Ruxolitinib [194], anti-influenza drug Favipiravir [195], antiviral drug Remdesivir [196][197][198], and most recently, a commonly used steroid, dexamethasone [199]. Many of these drugs primarily target the RdRp (NSP12) or the main protease, M pro . ...