Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

0

Genetic variegation of clonal architecture and stem cells in leukaemia


ABSTRACT: Little is known of the genetic architecture of cancer at the subclonal and single cell level or in the stem-like cells responsible for cancer clone maintenance and propagation. We have examined this issue in ALL in which ETV6-RUNX1 gene fuson is an early or initiating genetic lesion followed by a modest number of driver copy number alterations. By multiplexing FISH probes for these mutations, up to eight genetic abnormalities can be detected in single cells, a genetic signature of sub-clones identified and a composite picture of sub-clonal architecture and putative ancestral trees assembled. Sub-clones in ALL have variegated genetics and complex, non-linear or branching evolutionary histories. CNA are independently and recurrently acquired in sub-clones of individual patients, and in no preferential order. Clonal architecture is dynamic and changes in the lead up to a diagnosis and in relapse. Leukaemic stem cells, assayed by transplantation in NOD/SCID IL2Rgamma deficient mice, are also genetically variegated, mirroring sub-clonal patterns. These findings have significant implications for the cancer stem cell concept, for interpretation of cancer genome data and for therapeutic targetting in cancer. Mononuclear cells were isolated at diagnosis of ALL for patient #3 and #7. Transplantation of 2 000 - 2 000 000 unsorted leukaemia cells was performed by intra-tibial injection into 7 - 14 week old NOD/SCID IL2Rgamma deficient mice. Mice were sacrificed when peripheral blood engraftment was >2%. An equivalent of 2 000 - 200 000 CD45 cells were used for serial transplantation. DNA was extracted from mononuclear cells at initial diagnosis and after second transplantation. Copy number analysis of Affymetrix 500K SNP arrays was performed in CNAG 3.0 for patients #3 and #7 at initial diagnosis and after second transplantation. Reference files were 9 samples from leukemia in remission.

ORGANISM(S): Homo sapiens

SUBMITTER: Frederik van Delft 

PROVIDER: E-GEOD-24412 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

Similar Datasets

2010-12-16 | GSE24412 | GEO
2020-05-01 | GSE68623 | GEO
2022-12-30 | E-MTAB-11909 | biostudies-arrayexpress
2023-08-09 | E-MTAB-11375 | biostudies-arrayexpress
2023-08-09 | E-MTAB-11379 | biostudies-arrayexpress
2023-08-18 | E-MTAB-11376 | biostudies-arrayexpress
2021-04-18 | GSE151569 | GEO
2021-04-18 | GSE171833 | GEO
2021-04-18 | GSE151430 | GEO
2021-04-18 | GSE151357 | GEO