Clonal evolution in myelodysplastic syndromes
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28429724
PubMed Central
PMC5530598
DOI
10.1038/ncomms15099
PII: ncomms15099
Knihovny.cz E-zdroje
- MeSH
- buňky kostní dřeně účinky léků metabolismus patologie MeSH
- chemorezistence genetika MeSH
- GTP-fosfohydrolasy genetika metabolismus MeSH
- inhibitory angiogeneze terapeutické užití MeSH
- klonální evoluce účinky léků MeSH
- lenalidomid MeSH
- lidé středního věku MeSH
- lidé MeSH
- management nemoci MeSH
- membránové proteiny genetika metabolismus MeSH
- monitorování fyziologických funkcí MeSH
- mutace MeSH
- myelodysplastické syndromy farmakoterapie genetika metabolismus patologie MeSH
- nádorové biomarkery genetika metabolismus MeSH
- nádorový supresorový protein p53 genetika metabolismus MeSH
- následné studie MeSH
- progrese nemoci MeSH
- protoonkogenní proteiny p21(ras) genetika metabolismus MeSH
- regulace genové exprese u nádorů * MeSH
- sekvenování exomu MeSH
- senioři MeSH
- thalidomid analogy a deriváty terapeutické užití MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- GTP-fosfohydrolasy MeSH
- inhibitory angiogeneze MeSH
- KRAS protein, human MeSH Prohlížeč
- lenalidomid MeSH
- membránové proteiny MeSH
- nádorové biomarkery MeSH
- nádorový supresorový protein p53 MeSH
- NRAS protein, human MeSH Prohlížeč
- protoonkogenní proteiny p21(ras) MeSH
- thalidomid MeSH
- TP53 protein, human MeSH Prohlížeč
Cancer development is a dynamic process during which the successive accumulation of mutations results in cells with increasingly malignant characteristics. Here, we show the clonal evolution pattern in myelodysplastic syndrome (MDS) patients receiving supportive care, with or without lenalidomide (follow-up 2.5-11 years). Whole-exome and targeted deep sequencing at multiple time points during the disease course reveals that both linear and branched evolutionary patterns occur with and without disease-modifying treatment. The application of disease-modifying therapy may create an evolutionary bottleneck after which more complex MDS, but also unrelated clones of haematopoietic cells, may emerge. In addition, subclones that acquired an additional mutation associated with treatment resistance (TP53) or disease progression (NRAS, KRAS) may be detected months before clinical changes become apparent. Monitoring the genetic landscape during the disease may help to guide treatment decisions.
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