Related Experiment Videos
Repurposing SGLT2 Inhibitors Beyond Diabetes: Emerging Roles in Cancer Prevention and Therapy
Aarajana Shrestha1,2, Idelxy Perez3, Jasmine Miles4
1Department of Pharmaceutical Sciences, College of Pharmacy, Larkin University, Miami, FL, USA.
Abstract:
Sodium-glucose cotransporter 2 (SGLT2) inhibitors were originally developed as glucose-lowering agents for the management of type 2 diabetes mellitus. Nevertheless, accumulating evidence suggests that their therapeutic potential extends far beyond glycemic control, with emerging roles in cardiovascular and renal protection and, more recently, cancer prevention and therapy. This chapter explores the expanding landscape of SGLT2 inhibitors in oncology, highlighting the molecular mechanisms, preclinical evidence, and evolving clinical implications associated with their anticancer properties. Preclinical studies have demonstrated functional SGLT2 expression in several malignancies, including renal, pancreatic, prostate, liver, and breast cancers, where enhanced glucose uptake supports tumor growth and metabolic adaptation. By inhibiting glucose transport and altering cellular energy metabolism, SGLT2 inhibitors may suppress tumor proliferation, induce apoptosis, and reduce metastatic potential. Additionally, these agents display indirect anticancer effects through modulation of insulin resistance, reduction of chronic inflammation, attenuation of oxidative stress, and alteration of the tumor microenvironment. Emerging studies also suggest synergistic interactions between SGLT2 inhibitors and established anticancer therapies, including chemotherapy, immunotherapy, and targeted agents. Despite promising experimental findings, clinical evidence remains limited, and several challenges persist regarding optimal patient selection, tumor specificity, dosing strategies, and long-term safety in oncology settings. Furthermore, concerns of adverse effects such as ketoacidosis, genitourinary infections, and volume depletion warrant careful evaluation in cancer population. This review critically examines current knowledge regarding the mechanistic basis and translational potential of SGLT2 inhibitors as adjunctive or repurposed anticancer therapies. By incorporating findings from metabolic research, experimental oncology, and early clinical investigations, this chapter aims to provide a comprehensive overview of how SGLT2 inhibition may represent a novel and promising therapeutic avenue in precision cancer medicine.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Oral Hypoglycemic Agents: Biguanides and Glitazones
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Secondary Active Transport
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...