Published September 2022 | Version v1
Journal article

Coupling live-cell imaging and in situ isolation of the same single cell to profile the transient states of predicted drug-tolerant cells

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Description

Cell response variability is a starting point in cancer drug resistance that has been difficult to analyze because the tolerant cell states are short lived. Here, we present fate-seq, an approach to isolate single cells in their transient states of drug sensitivity or tolerance before profiling. The drug response is predicted in live cells, which are laser-captured by microdissection before any drug-induced change can alter their states. This framework enables the identification of the cell-state signatures causing differential cell decisions upon treatment.

Abstract

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Additional details

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URL
https://hal.science/hal-03860511
URN
urn:oai:HAL:hal-03860511v1

Origin repository

Origin repository
UNICA