TY - JOUR
T1 - Sodium-glucose cotransporter 2 inhibitors and the cancer patient: from diabetes to cardioprotection and beyond
AU - Camilli, Massimiliano
AU - Viscovo, Marcello
AU - Maggio, Luca
AU - Bonanni, Alice
AU - Torre, Ilaria
AU - Pellegrino, Claudio
AU - Lamendola, Priscilla
AU - Tinti, Lorenzo
AU - Teofili, Luciana
AU - Hohaus, Stefan
AU - Lanza, Gaetano Antonio
AU - Ferdinandy, Peter
AU - Varga, Zoltan
AU - Crea, Filippo
AU - Lombardo, Antonella
AU - Minotti, Giorgio
PY - 2024
Y1 - 2024
N2 - Sodium–glucose cotransporter 2 inhibitors (SGLT2i), a new drug class initially designed and approved for treatment of diabetes mellitus, have been shown to exert pleiotropic metabolic and direct cardioprotective and nephroprotective effects that extend beyond their glucose-lowering action. These properties prompted their use in two frequently intertwined conditions, heart failure and chronic kidney disease. Their unique mechanism of action makes SGLT2i an attractive option also to lower the rate of cardiac events and improve overall survival of oncological patients with preexisting cardiovascular risk and/or candidate to receive cardiotoxic therapies. This review will cover biological foundations and clinical evidence for SGLT2i modulating myocardial function and metabolism, with a focus on their possible use as cardioprotective agents in the cardio-oncology settings. Furthermore, we will explore recently emerged SGLT2i effects on hematopoiesis and immune system, carrying the potential of attenuating tumor growth and chemotherapy-induced cytopenias.
AB - Sodium–glucose cotransporter 2 inhibitors (SGLT2i), a new drug class initially designed and approved for treatment of diabetes mellitus, have been shown to exert pleiotropic metabolic and direct cardioprotective and nephroprotective effects that extend beyond their glucose-lowering action. These properties prompted their use in two frequently intertwined conditions, heart failure and chronic kidney disease. Their unique mechanism of action makes SGLT2i an attractive option also to lower the rate of cardiac events and improve overall survival of oncological patients with preexisting cardiovascular risk and/or candidate to receive cardiotoxic therapies. This review will cover biological foundations and clinical evidence for SGLT2i modulating myocardial function and metabolism, with a focus on their possible use as cardioprotective agents in the cardio-oncology settings. Furthermore, we will explore recently emerged SGLT2i effects on hematopoiesis and immune system, carrying the potential of attenuating tumor growth and chemotherapy-induced cytopenias.
KW - Cancer patients
KW - Cardio-oncology
KW - Sodium–glucose cotransporter 2 inhibitors
KW - Heart failure
KW - Cardioprotection
KW - Cancer patients
KW - Cardio-oncology
KW - Sodium–glucose cotransporter 2 inhibitors
KW - Heart failure
KW - Cardioprotection
UR - http://hdl.handle.net/10807/302239
U2 - 10.1007/s00395-024-01059-9
DO - 10.1007/s00395-024-01059-9
M3 - Article
SN - 0300-8428
SP - N/A-N/A
JO - Basic Research in Cardiology
JF - Basic Research in Cardiology
ER -