期刊文献+

肿瘤治疗相关心脏损伤诊断的研究进展 被引量:7

The diagnosis of cancer therapeutics-related cardiac dysfunction
下载PDF
导出
摘要 心脏损伤是胸部肿瘤放疗后或使用心脏毒性药物化疗后常见且严重的并发症。随着肿瘤治疗手段的改进以及药物的开发,患者总生存时间延长,很大一部分癌症患者带瘤生存甚至达到治愈,肿瘤治疗相关心脏损伤(CTRCD)的发生率和死亡率明显增高,严重影响着肿瘤患者的生存时间及生活质量。但是目前对于肿瘤治疗相关的心脏损伤尚无特异的标准或指南,尚难与原发性心脏疾病相鉴别。文章主要就肿瘤相关治疗后引起CTRCD的临床表现及诊断方法进行综述。 Cardiac dysfunction is a common and severe side-effect after cancer therapy including thoracic radiation or cytotoxic agents.With the development of the cancer therapy method and the agents,the survival time of the patients has improved while most cancer patients could live with tumor or even be cured.The rate of cancer therapeutics-related cardiac dysfunction have obviously increased which seriously affect the time and life quality of patients with tumor.But there are no authoritative consensus criteria or guideline to diagnose CTRCD at present while it is difficult to identify CTRCD with primary heart disease.In this article,we summarized some diagnosis methods which could identify early CTRCD,and then we may give early drug intervention as soon as possible to reduce the incidence and remission rate of cardiovascular events.
作者 徐芃 赖剑平 刘安文 XU Peng;LAI Jian-ping(reviewing);LIU An-wen(checking)(Department of Oncology,The Second Affiliated Hospital to Nanchang University,Nanchang 330006,Jiangxi,China)
出处 《医学研究生学报》 CAS 北大核心 2019年第4期437-442,共6页 Journal of Medical Postgraduates
关键词 心脏损伤 肿瘤治疗 诊断方法 cardiac dysfunction cancer therapy diagnose methods
  • 相关文献

参考文献2

二级参考文献36

  • 1Sonkoly E,Pivarcsi A.Advances in microRNAs:implications forimmunity and inflammatory diseasesCell Mol Med,2009.
  • 2Boehm M, Slack F. A developmental timing microRNA and its target regulate life span in C. elegans[J]. Science, 2005, 310 (5756) : 1954-1957.
  • 3Dimmeler S, Nicotera P. MicroRNAs in age-related disease[ J]. EMBO Mol Med, 2013, 5(2) : 180-190.
  • 4Suarez Y, Fernandez-Hemando C, Yu J, et al. Dicer dependent endothelial microRNAs are necessary for postnatal angiogenesis [J]. Proc Natl Acad Sci USA, 2008, 105(37) : 14082-14087.
  • 5Hu Z, Klein JD, Mitch WE, et al. MicroRNA-29 induces cellu- lar senescence in aging muscle through multiple signaling path- ways[J]. Aging (Albany NY), 2014, 6(3) : 160-175.
  • 6Fenn AM, Smith KM, Lovett-Racke AE, et al. Increased micro- RNA 29b in the aged brain correlates with the reduction of insu- lin-like growth factor-1 and fmctalkine ligand[J]. Neurobiol Ag- ing, 2013, 34(12): 2748-2758.
  • 7Boon RA, Seeger T, Heydt S, et al. MicroRNA-29 in aortic di- lation : implications for aneurysm formation [ J ]. Circ Res, 2011, 109(10) : 1115-1119.
  • 8Ugalde AP, Ramsay A J, de la Rosa J, et al. Aging and chronic DNA damage response activate a regulatory pathway involving miR-29 and p53[J]. EMBO J, 2011, 30(11) : 2219-2232.
  • 9Zhang P, Huang A, Ferruzzi J, et al. Inhibition of microRNA-29 enhances elastin levels in cells haploinsufficient for elastin and in bioengineered vessels-brief report [J]. Arterioseler Thremb Vase Biol, 2012, 32(3) : 756-759.
  • 10Tabuehi T, Satoh M, Itoh T, et al. MiereRNA-34a regulates the longevity-associated protein SIRT1 in coronary artery disease:effect of statins on SIRT1 and microRNA-34a expression [ J ]. Clin Sci (Lond), 2012, 123(3): 161-171.

共引文献14

同被引文献68

引证文献7

二级引证文献37

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部