摘要
当关于恶性胶质瘤(GB,WHO四级)的基础生物学,诊断和预后的理论知识在稳步提高时,其治疗方面的进步却缓慢得令人沮丧,近十年唯一有意义的新进展是在化疗中引入了替莫唑胺。为了分析GB临床研究的现状,我们在PubMed中用关键词“glioma AND trial”做了文献搜索,从2013年1月1日至2014年5月15日历时500天,我们回顾了I、II和III阶段的实验结果,其中也涉及到了儿科领域。最终我们得出结论:目前,和其他癌症研究领域一样,绝大多数关于恶性胶质瘤的临床前研究都没有转化为提高患者的存活率。为了探索这种致命肿瘤新的治疗方法,我们提议出两种新颖的药物化学方法:a) ATM抑制剂促进神经胶质瘤细胞对放疗的敏感性[1]。b) MYC抑制剂增强化疗药物对神经胶质瘤细胞的靶向性[2]。
关键词: 共济失调毛细管扩张突变,联合治疗,诊断,胶质瘤初始细胞,胶质瘤,抑制剂,MYC,预后,治疗
Current Medicinal Chemistry
Title:The Glioblastoma Problem: Targeting by Combined Medicinal Chemistry Approaches
Volume: 22 Issue: 21
Author(s): Guido Frosina
Affiliation:
关键词: 共济失调毛细管扩张突变,联合治疗,诊断,胶质瘤初始细胞,胶质瘤,抑制剂,MYC,预后,治疗
摘要: Whilst knowledge of basic biology, diagnosis and prognosis of glioblastoma (GB – WHO grade IV) are steadily improving, advancements of therapy are discouragingly slow, with the only significant novelty during last ten years represented by introduction of temozolomide in chemotherapy. In order to analyze the current status of clinical research on GB, a literature search was conducted in PubMed using the terms: “glioma AND trial” over a 500 day period elapsing from Jan 1, 2013 to May 15, 2014 and results of Phase I, II and III trials were reviewed. Results in the pediatric setting were included as well. It was concluded that, as in other cancer research areas, an overwhelming amount of pre-clinical research acquisitions in the GB field are not presently translated to improved patients’ survival. In order to explore novel therapeutic avenues for this deadly tumour, two innovative medicinal chemistry approaches are proposed and discussed: a) Specific glioma initiating cell-radiosensitization by ATM inhibitors [1] and b) Specific glioma initiating cell-chemotherapeutic targeting by MYC inhibitors [2].
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Cite this article as:
Guido Frosina , The Glioblastoma Problem: Targeting by Combined Medicinal Chemistry Approaches, Current Medicinal Chemistry 2015; 22 (21) . https://dx.doi.org/10.2174/0929867322666150530210700
DOI https://dx.doi.org/10.2174/0929867322666150530210700 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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