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Drug resistance: origins, evolution and characterization of genomic clones and the tumor ecosystem to optimize precise individualized therapy.

Published on Jun 1, 2019in Drug Discovery Today6.88
· DOI :10.1016/j.drudis.2019.04.008
Ioannis D Kyrochristos5
Estimated H-index: 5
,
Demosthenes E Ziogas6
Estimated H-index: 6
,
Dimitrios H Roukos6
Estimated H-index: 6
(Academy of Athens)
Sources
Abstract
Progress in understanding and overcoming fatal intrinsic and acquired resistance is slow, with only a few exceptions. Despite advances in modern genome and transcriptome analysis, the controversy of the three different theories on drug resistance and tumor progression, namely dynamic intratumor heterogeneity, pre-existing minor genomic clones and tumor ecosystem, is unresolved. Moreover, evidence on transcriptional heterogeneity suggests the necessity of a drug bank for individualized, precise drug-sensitivity prediction. We propose a cancer type- and stage-specific clinicogenomic and tumor ecosystemic concept toward cancer precision medicine, focusing on early therapeutic resistance and relapse.
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