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基于DNA损伤修复通路开发的新药及在泌尿系统肿瘤治疗中应用的研究进展
引用本文:李修明,曾宇. 基于DNA损伤修复通路开发的新药及在泌尿系统肿瘤治疗中应用的研究进展[J]. 现代肿瘤医学, 2022, 0(2): 322-325. DOI: 10.3969/j.issn.1672-4992.2022.02.031
作者姓名:李修明  曾宇
作者单位:1.承德医学院附属医院泌尿外科,河北 承德 067000;2.辽宁省肿瘤医院泌尿外科,辽宁 沈阳 110042
基金项目:国家自然科学基金资助项目(编号:81572532);辽宁省高等学校攀登学者优才计划。
摘    要:基因组不稳定性是癌症的一个重要特征,是由DNA损伤修复反应缺陷或复制压力增加引起的。这些缺陷也会变为癌细胞的弱点,人们可以利用这些弱点来提高抗癌治疗的效果。近年来,针对不同DNA损伤修复通路的高效选择性靶向制剂得到快速发展,人们已经观察到明确的抗肿瘤活性和药物安全性。临床医生应该认识到这类药物潜在的抗癌作用机制,包括药理学上的相似性和差异性,以及迄今报告的临床结果和毒副反应,这样才能为患者提供最优化的治疗方案。在此,我们将目前基于DNA损伤修复通路开发的新药与泌尿生殖系肿瘤的治疗现状进行综述。

关 键 词:DNA损伤修复  DNA损伤应答  泌尿生殖系肿瘤  抗肿瘤作用

Research progress of new drugs developed by DNA damage repair pathway and their application in the treatment of urogenital neoplasms
LI Xiuming,ZENG Yu. Research progress of new drugs developed by DNA damage repair pathway and their application in the treatment of urogenital neoplasms[J]. Journal of Modern Oncology, 2022, 0(2): 322-325. DOI: 10.3969/j.issn.1672-4992.2022.02.031
Authors:LI Xiuming  ZENG Yu
Affiliation:1.Department of Urology,the Affiliated Hospital of Chengde Medical University,Hebei Chengde 067000,China;2.Department of Urology,Liaoning Cancer Hospital and Institute,Liaoning Shenyang 110042,China.
Abstract:Genomic instability is an important feature of cancer and is caused by defective response to DNA damage or increased replication pressure.These defects can also become weaknesses of cancer cells that can be exploited to improve the effectiveness of anti-tumor treatments.In recent years,targeted drugs for DNA damage repair pathways have been developed rapidly,and anti-tumor activity and drug safety have been observed.Clinicians should be aware of the potential anti-tumor mechanisms of such drugs,including pharmacological similarities and differences,as well as the clinical results and side effects reported to date,in order to provide patients with optimal treatment options.Here,we summarize the current status of new drugs developed by DNA damage repair pathway and treatment of urogenital neoplasms.
Keywords:DNA damage repair  DNA damage response  urogenital neoplasms  anti-tumor effect
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