NQO1 is a 30–33 kDa flavoprotein that catalyzes the two-electron reduction of quinones and nitroaromatics using NAD(P)H as an electron donor . Key functions include:
Antioxidant Defense: Protects against oxidative stress by reducing reactive quinones and preventing semi-quinone radical formation .
Protein Stabilization: Binds and stabilizes tumor suppressors like p53, delaying proteasomal degradation .
NAD+ Homeostasis: Modulates NAD+/NADH ratios, influencing DNA repair mechanisms via PARP and sirtuin activation .
Disease Modulation: Linked to cardiovascular diseases, diabetic nephropathy, and cancer progression .
Therapeutic Targeting: NQO1 overexpression in tumors correlates with poor prognosis. Antibodies identify NQO1-positive cells for targeted therapies like β-lapachone, which induces NAD+ depletion and necrosis in cancer .
Biomarker Validation: Used to validate NQO1 as a biomarker in colorectal cancer (CRC) via immunohistochemistry (IHC) .
Diabetic Nephropathy: NQO1 antibodies confirm its role in reducing oxidative stress and apoptosis by regulating Sirt1/NAD+ pathways .
Atherosclerosis: Studies link NQO1 activity to reduced lipid peroxidation and inflammation in vascular tissues .
Cancer Therapy: NQO1 bioactivates prodrugs like β-lapachone, causing selective cytotoxicity in NQO1-rich tumors .
Oxidative Stress Disorders: Antibodies aid in tracking NQO1’s protective effects in diabetes and cardiovascular diseases .