Functional screens on single-cell transcriptomes of genotypically-defined minimal residual disease cells to unravel specific vulnerabilities of treatment resistant multiple myeloma (FUTURE)
Basic Information
Description
The research proposed in this grant stems from
the hypothesis that phenotypic hierarchies between distinct clonal cells may explain MM ontogeny
and relapse patterns, and that through innovative approaches this can be harnessed to provide better
biomarkers of treatment response and vulnerabilities to eradicate residual cells. I propose an unbiased
simultaneous analysis of B-cell receptor (BCR) sequence and whole-transcriptome from single cells, using
innovative approaches to deconvolute heterogeneity and opening a new frontier of functional analysis of
genetic and phenotypic determinants of disease evolution from diagnosis to minimal residual disease (MRD).