Repurposing FDA-Approved Drugs as Fructosamine-3-Kinase Inhibitors: A
                    Mechanistic and Translational Approach to Redox-Driven Cancer
                    Therapy

Erica Alves; Gurupadayya Bannimath; Prabitha Prabhakaran

doi:10.1055/a-2677-4956

Drug Research, Inhaltsverzeichnis

Drug Res (Stuttg)
DOI: 10.1055/a-2677-4956

Review

Repurposing FDA-Approved Drugs as Fructosamine-3-Kinase Inhibitors: A Mechanistic and Translational Approach to Redox-Driven Cancer Therapy

Authors

Erica Alves

¹Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysore, India
Gurupadayya Bannimath

¹Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysore, India
Prabitha Prabhakaran

¹Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysore, India

Abstract

Fructosamine-3-kinase (FN3K), a deglycating enzyme originally studied in the context of diabetes, has recently emerged as a pivotal modulator of redox homeostasis and therapeutic resistance in cancer. FN3K catalyzes the removal of early glycation adducts, thereby stabilizing redox-sensitive proteins such as Nuclear factor erythroid 2–related factor 2 (Nrf2), a key transcriptional regulator of antioxidant defense. This review explores the evolving role of FN3K in tumor metabolism, highlighting its expression patterns across cancer types, structural features amenable to therapeutic targeting, and mechanistic interplay with the Nrf2 pathway. Emphasis is placed on FDA-approved drugs with FN3K-modulatory potential, evaluated through computational modeling, docking simulations, and structure – activity insights. The analysis reveals a dual opportunity: to repurpose redox-active agents as FN3K inhibitors and to exploit FN3K as a biomarker for redox stratification in precision oncology. Despite promising in silico data and preclinical correlations, challenges remain – particularly in achieving target selectivity, overcoming structural limitations, and validating pharmacodynamic markers. Addressing these barriers through integrated translational strategies could unlock FN3K as a tractable node in redox-driven cancer therapy.

Keywords

fructosamine-3-kinase (FN3K) - redox homeostasis - Nrf2 signaling - cancer metabolism - drug repurposing - deglycation - computational modeling - precision oncology

Volltext

Referenzen

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