Evidence map›Paper›PMID 32710494›Full record

ArticleFEBS open bio2020

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

Alfred G Tamayo, Syukri Shukor, Alexandra Burr, Patrick Erickson, Biju Parekkadan

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 51% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Allometric-like scaling of AAV gene therapy for systemic protein delivery.Molecular therapy. Methods & clinical development · 2022
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Alfred G TamayoCenter for Surgery, Innovation, and Bioengineering, Department of Surgery, Harvard Medical School, Massachusetts General Hospital, Shriners Hospitals for Children, Boston, MA, USA.ORCID 0000-0002-2321-0831
Syukri ShukorCenter for Surgery, Innovation, and Bioengineering, Department of Surgery, Harvard Medical School, Massachusetts General Hospital, Shriners Hospitals for Children, Boston, MA, USA.
Alexandra BurrDepartment of Biomedical Engineering, Rutgers University, Piscataway, NJ, USA.ORCID 0000-0002-7954-3619
Patrick EricksonDepartment of Biomedical Engineering, Rutgers University, Piscataway, NJ, USA.ORCID 0000-0003-1303-3701
Biju ParekkadanCenter for Surgery, Innovation, and Bioengineering, Department of Surgery, Harvard Medical School, Massachusetts General Hospital, Shriners Hospitals for Children, Boston, MA, USA.
Rutgers, The State University of New Jersey · USShriners Hospitals for Children - Erie · US

Funding

X-RAY STRUCTURE OF RIFM PROTEIN FROM THE BIOSYNTHESIS PATHWAY OF THE ANSAMYCIN AP41RR012408 · NCRR · BROOKHAVEN SCIENCE ASSOC-BROOKHAVEN LAB · PI MARIUZZA, ROY A · 1998 to 2011
$32.2M
UMDNJ TRAINING GRANT IN BIOTECHNOLOGYT32GM008339 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI YARMUSH, MARTIN L · 1989 to 2019
$6.1M
Artificial, Humanized Stem Cell NichesR01EB012521 · NIBIB · RUTGERS, THE STATE UNIV OF N.J. · PI PAREKKADAN, BIJU · 2011 to 2021
$6.0M
Rutgers Biotechnology Training ProgramT32GM135141 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI ANN M. STOCK, Martin L Yarmush · 2020 to 2026
$3.5M
A Functional genomics platform with integrated library cloning and molecular displayR01GM127353 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LARMAN, HARRY BENJAMIN, PAREKKADAN, BIJU · 2018 to 2021
$1.4M
Theranostic approach to transplant rejection using engineered cell biosensorsR21AI134116 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI PAREKKADAN, BIJU, UYGUN, KORKUT · 2018 to 2019
$463k
NCRR NIH HHS P41 RR012408NIAID NIH HHS R21 AI134116NIBIB NIH HHS R01 EB012521NIGMS NIH HHS R01 GM127353NIGMS NIH HHS T32 GM008339NIGMS NIH HHS T32 GM135141NIH HHS R21AI13411
6 · The paper itself

Abstract

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.

Indexed as

Cells, CulturedHumansJurkat CellsLuciferasesT-LymphocytesLuciferasescircadian clocksleukemic T cellssecreted luciferasetranscriptional reporter

Identifiers

PMID32710494
PMCPMC7459418
OpenAlexW3045422174

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.