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Adverse stem cell clones within a single patient's tumor predict clinical outcome in AML patients.


ABSTRACT: Acute myeloid leukemia (AML) patients suffer dismal prognosis upon treatment resistance. To study functional heterogeneity of resistance, we generated serially transplantable patient-derived xenograft (PDX) models from one patient with AML and twelve clones thereof, each derived from a single stem cell, as proven by genetic barcoding. Transcriptome and exome sequencing segregated clones according to their origin from relapse one or two. Undetectable for sequencing, multiplex fluorochrome-guided competitive in vivo treatment trials identified a subset of relapse two clones as uniquely resistant to cytarabine treatment. Transcriptional and proteomic profiles obtained from resistant PDX clones and refractory AML patients defined a 16-gene score that was predictive of clinical outcome in a large independent patient cohort. Thus, we identified novel genes related to cytarabine resistance and provide proof of concept that intra-tumor heterogeneity reflects inter-tumor heterogeneity in AML.

SUBMITTER: Zeller C 

PROVIDER: S-EPMC8917742 | biostudies-literature | 2022 Mar

REPOSITORIES: biostudies-literature

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Adverse stem cell clones within a single patient's tumor predict clinical outcome in AML patients.

Zeller Christina C   Richter Daniel D   Jurinovic Vindi V   Valtierra-Gutiérrez Ilse A IA   Jayavelu Ashok Kumar AK   Mann Matthias M   Bagnoli Johannes W JW   Hellmann Ines I   Herold Tobias T   Enard Wolfgang W   Vick Binje B   Jeremias Irmela I  

Journal of hematology & oncology 20220312 1


Acute myeloid leukemia (AML) patients suffer dismal prognosis upon treatment resistance. To study functional heterogeneity of resistance, we generated serially transplantable patient-derived xenograft (PDX) models from one patient with AML and twelve clones thereof, each derived from a single stem cell, as proven by genetic barcoding. Transcriptome and exome sequencing segregated clones according to their origin from relapse one or two. Undetectable for sequencing, multiplex fluorochrome-guided  ...[more]

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