Intratumoral heterogeneity: pathways to treatment resistance and relapse in human glioblastoma

被引:268
|
作者
Qazi, M. A. [1 ,2 ]
Vora, P. [1 ,3 ]
Venugopal, C. [1 ,3 ]
Sidhu, S. S. [4 ,5 ]
Moffat, J. [4 ,5 ]
Swanton, C. [6 ]
Singh, S. K. [1 ,2 ,3 ]
机构
[1] McMaster Univ, Stem Cell & Canc Res Inst, 1280 Main St West, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON, Canada
[3] McMaster Univ, Dept Surg, Hamilton, ON, Canada
[4] Univ Toronto, Donnelly Ctr, Toronto, ON, Canada
[5] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[6] Univ Coll London Inst, Francis Crick Inst, London, England
关键词
glioblastoma; intratumoral heterogeneity; brain tumor initiating cells; recurrence; models of resistance; polytherapy; CANCER STEM-CELLS; ADJUVANT TEMOZOLOMIDE; SELF-RENEWAL; EVOLUTION; REVEALS; GLIOMA; RADIOTHERAPY; DYNAMICS; THERAPY; GROWTH;
D O I
10.1093/annonc/mdx169
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Intratumoral heterogeneity (ITH) has increasingly being described for multiple cancers as the root cause of therapy resistance. Recent studies have started to explore the scope of ITH in glioblastoma (GBM), a highly aggressive and fatal form of brain tumor, to explain its inevitable therapy resistance and disease relapse. In this review, we detail the emerging data that explores the extensive genetic, cellular and functional ITH present in GBM. We discuss current experimental models of human GBM recurrence and suggest harnessing new technologies (CRISPR-Cas9 screening, CyTOF, cellular barcoding, single cell analysis) to delineate GBM ITH and identify treatment-refractory cell populations, thus opening new therapeutic windows. We will also explore why current therapeutics have failed in clinical trials and how ITH can inform us on developing empiric therapies for the treatment of recurrent GBM.
引用
收藏
页码:1448 / 1456
页数:9
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