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Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay

Transcriptional dynamics of cancer cells govern cell fate decisions and are therapeutically actionable drug targets. In this study, we engineered a circulating cancer cell line that secretes a luciferase reporter to capture constitutive and circadian clock‐driven transcription dynamics over the cour...

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Autores principales: Tamayo, Alfred G., Shukor, Syukri, Burr, Alexandra, Erickson, Patrick, Parekkadan, Biju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459418/
https://www.ncbi.nlm.nih.gov/pubmed/32710494
http://dx.doi.org/10.1002/2211-5463.12940
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author Tamayo, Alfred G.
Shukor, Syukri
Burr, Alexandra
Erickson, Patrick
Parekkadan, Biju
author_facet Tamayo, Alfred G.
Shukor, Syukri
Burr, Alexandra
Erickson, Patrick
Parekkadan, Biju
author_sort Tamayo, Alfred G.
collection PubMed
description Transcriptional dynamics of cancer cells govern cell fate decisions and are therapeutically actionable drug targets. In this study, we engineered a circulating cancer cell line that secretes a luciferase reporter to capture constitutive and circadian clock‐driven transcription dynamics over the course of a day. Engineered human leukemic T cells (Jurkat) were observed to rhythmically secrete luciferase in a continuous flow cell culture system. When transplanted in vivo, engineered leukemic cells caused circadian plasma luciferase activity and had expected pathological signs of leukemic disease. This technique is rapid and noninvasive, requiring only a few microliters of media or blood, and can aid in investigating relationships between in vivo cancer cell signaling and behavior, such as diet or sleep.
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spelling pubmed-74594182020-09-03 Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay Tamayo, Alfred G. Shukor, Syukri Burr, Alexandra Erickson, Patrick Parekkadan, Biju FEBS Open Bio Research Articles Transcriptional dynamics of cancer cells govern cell fate decisions and are therapeutically actionable drug targets. In this study, we engineered a circulating cancer cell line that secretes a luciferase reporter to capture constitutive and circadian clock‐driven transcription dynamics over the course of a day. Engineered human leukemic T cells (Jurkat) were observed to rhythmically secrete luciferase in a continuous flow cell culture system. When transplanted in vivo, engineered leukemic cells caused circadian plasma luciferase activity and had expected pathological signs of leukemic disease. This technique is rapid and noninvasive, requiring only a few microliters of media or blood, and can aid in investigating relationships between in vivo cancer cell signaling and behavior, such as diet or sleep. John Wiley and Sons Inc. 2020-08-12 /pmc/articles/PMC7459418/ /pubmed/32710494 http://dx.doi.org/10.1002/2211-5463.12940 Text en © 2020 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Tamayo, Alfred G.
Shukor, Syukri
Burr, Alexandra
Erickson, Patrick
Parekkadan, Biju
Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title_full Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title_fullStr Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title_full_unstemmed Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title_short Tracking leukemic T‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
title_sort tracking leukemic t‐cell transcriptional dynamics in vivo with a blood‐based reporter assay
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459418/
https://www.ncbi.nlm.nih.gov/pubmed/32710494
http://dx.doi.org/10.1002/2211-5463.12940
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