AI Article Synopsis

  • Diabetes is linked to serious health issues, including skin problems and a higher risk of certain cancers, particularly hematological malignancies.
  • The study focused on the compound 2'-Hydroxy-4',5'-dimethoxyacetophenone, which was found to inhibit aldose reductase and collagenase enzymes, and showed strong anti-leukemic effects in various human acute leukemia cell lines.
  • Results indicated that this compound not only effectively targets cancer cells without toxicity to normal cells but also demonstrated significant antioxidant activity, showcasing its potential pharmacological benefits.

Article Abstract

Diabetes is a serious growing concern that affects many parts of the body including the skin due to high sugar levels. Moreover, diabetic patients are at risk of developing cancer and are prone to a higher risk of hematological malignancies. In the present study, the inhibitory effect of 2'-Hydroxy-4',5'-dimethoxyacetophenone was investigated on aldose reductase and collagenase enzymes, along with docking and ADMET analysis. MTT assay was also conducted to investigate the anti-leukemic effect of 2'-Hydroxy-4',5'-dimethoxyacetophenone on human acute leukemia cells (32D-FLT3-ITD, Human HL-60/vcr, MOLT-3, and TALL-104 cell lines) and DPPH assay for establishing activity against oxidative stress. The 2'-Hydroxy-4',5'-dimethoxyacetophenone showed potent inhibition of both the above tested enzymes with numerous strong interactions with the key catalytic residues in the active site of the enzymes. The MTT assay showed strong anti-cancer activity against entire tested human acute leukemia cells and was found non-toxic to normal (HUVEC) at the tested concentration. In DPPH free radical scavenging assay, 2'-Hydroxy-4',5'-dimethoxyacetophenone showed strong inhibitory activity with IC of 157 µg/mL, which found comparable to the standard BHT. Our study demonstrated prominent pharmacological benefit of 2'-Hydroxy-4',5'-dimethoxyacetophenone, against various leukemic cell lines, aldose reductase and collagenase enzymes, and free radical scavenging activity.

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http://dx.doi.org/10.1007/s12033-022-00588-9DOI Listing

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