治疗无效的恶性肿瘤导致心血管疾病:最先进的心脏病肿瘤学视角

Leslie M. Ogilvie, Bridget Coyle-Asbil, Keith R. Brunt, Jim Petrik, Jeremy A. Simpson
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引用次数: 0

摘要

心血管疾病(CVD)和癌症是导致全球死亡的主要原因。虽然心血管疾病和癌症通常被认为是不同的疾病,但它们之间的交叉重叠在因果关系和机理关系上都越来越明显。心脏病肿瘤学领域主要关注癌症疗法(如化疗、放疗)对心脏的毒性影响。此外,心脏毒性疗法暴露的累积效应和癌症患者普遍存在的心血管疾病风险因素导致了这一患者群体的长期发病率和较差的生活质量--即使患者已不再罹患癌症。来自癌症患者和动物模型的证据表明,恶性肿瘤本身(与心脏毒性治疗暴露或心血管疾病危险因素无关)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无效癌症的心脏病理生理学和分子特征。我们还总结了用于心脏肿瘤学研究的临床前癌症模型的优势和局限性,并讨论了已通过实验测试的治疗癌症诱发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,即 "反向心因肿瘤学",在这一领域中,心力衰竭的后遗症会加剧癌症的进展。在此,我们强调恶性肿瘤与受伤心脏之间的跨疾病交流,并讨论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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapy-naïve malignancy causes cardiovascular disease: A state-of-the-art cardio-oncology perspective
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 cardiotoxic effects of cancer therapies (e.g., chemotherapy, radiation). Further, the cumulative effects of cardiotoxic therapy exposure and the prevalence of CVD risk factors in cancer patients leads to long-term morbidity and poor quality of life in this patient population-even when patients are cancer-free. Evidence from cancer patients 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 pathophysiologic 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.
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