Department of Human Health and Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada.
Department of Pharmacology, Dalhousie Medicine New Brunswick, Saint John, New Brunswick, Canada.
Am J Physiol Heart Circ Physiol. 2024 Jun 1;326(6):H1515-H1537. doi: 10.1152/ajpheart.00795.2023. Epub 2024 Apr 19.
Cardiovascular disease (CVD) and cancer are the leading causes of mortality worldwide. Although generally thought of as distinct diseases, the intersectional overlap between CVD and cancer is increasingly evident in both causal and mechanistic relationships. The field of cardio-oncology is largely focused on the cardiotoxic effects of cancer therapies (e.g., chemotherapy, radiation). Furthermore, the cumulative effects of cardiotoxic therapy exposure and the prevalence of CVD risk factors in patients with cancer lead to long-term morbidity and poor quality of life in this patient population, even when patients are cancer-free. Evidence from patients with cancer and animal models demonstrates that the presence of malignancy itself, independent of cardiotoxic therapy exposure or CVD risk factors, negatively impacts cardiac structure and function. As such, the primary focus of this review is the cardiac pathophysiological and molecular features of therapy-naïve cancer. We also summarize the strengths and limitations of preclinical cancer models for cardio-oncology research and discuss therapeutic strategies that have been tested experimentally for the treatment of cancer-induced cardiac atrophy and dysfunction. Finally, we explore an adjacent area of interest, called "reverse cardio-oncology," where the sequelae of heart failure augment cancer progression. Here, we emphasize the cross-disease communication between malignancy and the injured heart and discuss the importance of chronic low-grade inflammation and endocrine factors in the progression of both diseases.
心血管疾病 (CVD) 和癌症是全球主要的死亡原因。尽管通常被认为是两种截然不同的疾病,但 CVD 和癌症之间在因果和机制关系上的交叉重叠越来越明显。肿瘤心脏病学领域主要关注癌症治疗的心脏毒性作用(例如化疗、放疗)。此外,心脏毒性治疗暴露的累积效应以及癌症患者中 CVD 风险因素的流行导致了该患者群体的长期发病率和生活质量下降,即使患者已经没有癌症。来自癌症患者和动物模型的证据表明,恶性肿瘤本身的存在,独立于心脏毒性治疗暴露或 CVD 风险因素,会对心脏结构和功能产生负面影响。因此,本综述的主要重点是治疗初治癌症的心脏病理生理和分子特征。我们还总结了用于肿瘤心脏病学研究的临床前癌症模型的优缺点,并讨论了已经在实验中测试过的用于治疗癌症诱导的心脏萎缩和功能障碍的治疗策略。最后,我们探讨了一个相邻的研究领域,称为“反向肿瘤心脏病学”,其中心力衰竭的后遗症会增加癌症的进展。在这里,我们强调了恶性肿瘤和受损心脏之间的疾病交叉通讯,并讨论了慢性低度炎症和内分泌因素在这两种疾病进展中的重要性。