Cardiac-specific overexpression of glucose-regulated protein 78 or administration of the chemical ER chaperone 4-phenylbutyrate alleviated doxorubicin-induced cardiac apoptosis and dysfunction.
Does overexpression of glucose-regulated protein 78 or administration of 4-phenylbutyrate alleviate doxorubicin-induced cardiac dysfunction in mouse models?
Overexpression of GRP78 or administration of a chemical ER chaperone alleviates doxorubicin-induced cardiac dysfunction in preclinical models, suggesting a potential therapeutic strategy for preventing chemotherapy-induced cardiotoxicity.
RATIONALE: Doxorubicin is an effective chemotherapeutic agent for cancer, but its use is often limited by cardiotoxicity. Doxorubicin causes endoplasmic reticulum (ER) dilation in cardiomyocytes, and we have demonstrated that ER stress plays important roles in the pathophysiology of heart failure. OBJECTIVE: We evaluated the role of ER stress in doxorubicin-induced cardiotoxicity and examined whether the chemical ER chaperone could prevent doxorubicin-induced cardiac dysfunction. METHODS AND RESULTS: We confirmed that doxorubicin caused ER dilation in mouse hearts, indicating that doxorubicin may affect ER function. Doxorubicin activated an ER transmembrane stress sensor, activating transcription factor 6, in cultured cardiomyocytes and mouse hearts. However, doxorubicin suppressed the expression of genes downstream of activating transcription factor 6, including X-box binding protein 1. The decreased levels of X-box binding protein 1 resulted in a failure to induce the expression of the ER chaperone glucose-regulated protein 78 which plays a major role in adaptive responses to ER stress. In addition, doxorubicin activated caspase-12, an ER membrane-resident apoptotic molecule, which can lead to cardiomyocyte apoptosis and cardiac dysfunction. Cardiac-specific overexpression of glucose-regulated protein 78 by adeno-associated virus 9 or the administration of the chemical ER chaperone 4-phenylbutyrate attenuated caspase-12 cleavage, and alleviated cardiac apoptosis and dysfunction induced by doxorubicin. CONCLUSIONS: Doxorubicin activated the ER stress-initiated apoptotic response without inducing the ER chaperone glucose-regulated protein 78, further augmenting ER stress in mouse hearts. Cardiac-specific overexpression of glucose-regulated protein 78 or the administration of the chemical ER chaperone alleviated the cardiac dysfunction induced by doxorubicin and may facilitate the safe use of doxorubicin for cancer treatment.
Fu et al. (Mon,) conducted a other in Doxorubicin-induced cardiotoxicity. Cardiac-specific overexpression of glucose-regulated protein 78 or chemical ER chaperone 4-phenylbutyrate was evaluated on Cardiac apoptosis and dysfunction. Cardiac-specific overexpression of glucose-regulated protein 78 or administration of the chemical ER chaperone 4-phenylbutyrate alleviated doxorubicin-induced cardiac apoptosis and dysfunction.