Cupit-Link Margaret C, Kirkland James L, Ness Kirsten K, Armstrong Gregory T, Tchkonia Tamar, LeBrasseur Nathan K, Armenian Saro H, Ruddy Kathryn J, Hashmi Shahrukh K
College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.
ESMO Open. 2017 Dec 18;2(5):e000250. doi: 10.1136/esmoopen-2017-000250. eCollection 2017.
Over 30 million cancer survivors exist worldwide. Survivors have an earlier onset and higher incidence of chronic comorbidities, including endocrinopathies, cardiac dysfunction, osteoporosis, pulmonary fibrosis, secondary cancers and frailty than the general population; however, the fundamental basis of these changes at the cellular level is unknown. An electronic search was performed on Embase, Medline In-Process & Other Non-Indexed Citations, and the Cochrane Central Register of Controlled Trials. Original articles addressing the cellular biology of ageing and/or the mechanisms of cancer therapies similar to ageing mechanisms were included, and references of these articles were reviewed for further search. We found multiple biological process of ageing at the cellular level and their association with cancer therapies, as well as with clinical effects. The direct effects of various chemotherapies and radiation on telomere length, senescent cells, epigenetic modifications and microRNA were found. We review the effects of cancer therapies on recognised hallmarks of ageing. Long-term comorbidities seen in cancer survivors mimic the phenotypes of ageing and likely result from the interaction between therapeutic exposures and the underlying biology of ageing. Long-term follow-up of cancer survivors and research on prevention strategies should be pursued to increase the length and quality of life among the growing population of cancer survivors.
全球有超过3000万癌症幸存者。与普通人群相比,幸存者慢性合并症的发病更早且发病率更高,包括内分泌疾病、心脏功能障碍、骨质疏松症、肺纤维化、继发性癌症和身体虚弱;然而,这些细胞水平变化的根本原因尚不清楚。我们在Embase、Medline In-Process & Other Non-Indexed Citations以及Cochrane对照试验中央注册库进行了电子检索。纳入了探讨衰老细胞生物学和/或与衰老机制相似的癌症治疗机制的原始文章,并对这些文章的参考文献进行了回顾以进一步检索。我们发现了细胞水平上衰老的多个生物学过程及其与癌症治疗以及临床效果的关联。发现了各种化疗和放疗对端粒长度、衰老细胞、表观遗传修饰和微小RNA的直接影响。我们综述了癌症治疗对公认的衰老特征的影响。癌症幸存者中出现的长期合并症类似于衰老的表型,可能是治疗暴露与潜在衰老生物学相互作用的结果。应开展癌症幸存者的长期随访和预防策略研究,以提高不断增加的癌症幸存者群体的寿命和生活质量。