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Targeting the metastatic niche: Single-cell lineage tracing in prime time

Identification of actionable drug targets remains a rate-limiting step of, and one of the most prominent barriers to successful drug development for metastatic cancers. CRISPR-Cas9, a tool for making targeted genomic edits, has given rise to various novel applications that have greatly accelerated d...

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Autores principales: Sommer, Elijah R., Napoli, Giulia C., Chau, Cindy H., Price, Douglas K., Figg, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988656/
https://www.ncbi.nlm.nih.gov/pubmed/36895653
http://dx.doi.org/10.1016/j.isci.2023.106174
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author Sommer, Elijah R.
Napoli, Giulia C.
Chau, Cindy H.
Price, Douglas K.
Figg, William D.
author_facet Sommer, Elijah R.
Napoli, Giulia C.
Chau, Cindy H.
Price, Douglas K.
Figg, William D.
author_sort Sommer, Elijah R.
collection PubMed
description Identification of actionable drug targets remains a rate-limiting step of, and one of the most prominent barriers to successful drug development for metastatic cancers. CRISPR-Cas9, a tool for making targeted genomic edits, has given rise to various novel applications that have greatly accelerated discovery in developmental biology. Recent work has coupled a CRISPR-Cas9-based lineage tracing platform with single-cell transcriptomics in the unexplored context of cancer metastasis. In this perspective, we briefly reflect on the development of these distinct technological advances and the process by which they have become integrated. We also highlight the importance of single-cell lineage tracing in oncology drug development and suggest the profound capacity of a high-resolution, computational approach to reshape cancer drug discovery by enabling identification of novel metastasis-specific drug targets and mechanisms of resistance.
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spelling pubmed-99886562023-03-08 Targeting the metastatic niche: Single-cell lineage tracing in prime time Sommer, Elijah R. Napoli, Giulia C. Chau, Cindy H. Price, Douglas K. Figg, William D. iScience Perspective Identification of actionable drug targets remains a rate-limiting step of, and one of the most prominent barriers to successful drug development for metastatic cancers. CRISPR-Cas9, a tool for making targeted genomic edits, has given rise to various novel applications that have greatly accelerated discovery in developmental biology. Recent work has coupled a CRISPR-Cas9-based lineage tracing platform with single-cell transcriptomics in the unexplored context of cancer metastasis. In this perspective, we briefly reflect on the development of these distinct technological advances and the process by which they have become integrated. We also highlight the importance of single-cell lineage tracing in oncology drug development and suggest the profound capacity of a high-resolution, computational approach to reshape cancer drug discovery by enabling identification of novel metastasis-specific drug targets and mechanisms of resistance. Elsevier 2023-02-10 /pmc/articles/PMC9988656/ /pubmed/36895653 http://dx.doi.org/10.1016/j.isci.2023.106174 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Perspective
Sommer, Elijah R.
Napoli, Giulia C.
Chau, Cindy H.
Price, Douglas K.
Figg, William D.
Targeting the metastatic niche: Single-cell lineage tracing in prime time
title Targeting the metastatic niche: Single-cell lineage tracing in prime time
title_full Targeting the metastatic niche: Single-cell lineage tracing in prime time
title_fullStr Targeting the metastatic niche: Single-cell lineage tracing in prime time
title_full_unstemmed Targeting the metastatic niche: Single-cell lineage tracing in prime time
title_short Targeting the metastatic niche: Single-cell lineage tracing in prime time
title_sort targeting the metastatic niche: single-cell lineage tracing in prime time
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988656/
https://www.ncbi.nlm.nih.gov/pubmed/36895653
http://dx.doi.org/10.1016/j.isci.2023.106174
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