Key result
Dysbiosis of intestinal microecology may serve as a potential mechanism and therapeutic target for the prevention and treatment of antitumor therapy-related cardiotoxicity.
Why the study?
Antitumor-related cardiotoxicity is a leading cause of long-term mortality in malignancy patients, but its pathogenesis remains unclear and practical preventive and therapeutic strategies are lacking.
Can targeting intestinal microecology prevent or treat antitumor therapy-related cardiotoxicity in patients with malignancies?
Can targeting intestinal microecology prevent or treat antitumor therapy-related cardiotoxicity in patients with malignancies?
Intestinal microecology dysbiosis is proposed as a potential mechanism and therapeutic target for preventing and treating antitumor therapy-related cardiotoxicity.
Should not yet change cardio-oncology practice; leaves open gut microbiota as a target for antitumor cardiotoxicity.
The continuous development of antitumor therapy has significantly reduced the mortality of patients with malignancies. However, the antitumor-related cardiotoxicity has become the leading cause of long-term mortality in patients with malignancies. Besides, the pathogenesis of antitumor-related cardiotoxicity is still unclear, and practical means of prevention and treatment are lacking in clinical practice. Therefore, the major challenge is how to combat the cardiotoxicity of antitumor therapy effectively. More and more studies have shown that antitumor therapy kills tumor cells while causing damage to sensitive tissues such as the intestinal mucosa, leading to the increased permeability of the intestine and the dysbiosis of intestinal microecology. In addition, the dysbiosis of intestinal microecology contributes to the development and progression of cardiovascular diseases through multiple pathways. Thus, the dysbiosis of intestinal microecology may be a potential mechanism and target for antitumor-related cardiotoxicity. We summarized the characteristics of intestinal microecology disorders induced by antitumor therapy and the association between intestinal microecological dysbiosis and CVD. And on this basis, we hypothesized the potential mechanisms of intestinal microecology mediating the occurrence of antitumor-related cardiotoxicity. Then we reviewed the previous studies targeting intestinal microecology against antitumor-associated cardiotoxicity, aiming to provide a reference for future studies on the occurrence and prevention of antitumor-related cardiotoxicity by intestinal microecology.
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Meng et al. (2023) conducted a review in Antitumor therapy-related cardiotoxicity. Intestinal microecology was evaluated. Dysbiosis of intestinal microecology may serve as a potential mechanism and therapeutic target for the prevention and treatment of antitumor therapy-related cardiotoxicity.
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