Evidence map›Paper›PMID 40453140›Full record

ArticleBlood neoplasia2025

A feedforward loop between ACLY and MYC supports T-ALL progression in vivo.

Victoria da Silva-Diz, Amartya Singh, Maya Aleksandrova, Oekyung Kim, Christopher Thai, Olga Lancho, Patricia Renck Nunes, Hayley Affronti, Alexia Martínez de Paz, Steven Z Josefowicz and 3 more

Abstract read
In one paragraph

Article in Blood neoplasia, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. A dietary pan-amino acid dropout screenbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Victoria da Silva-DizRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Amartya SinghRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Maya AleksandrovaRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Oekyung KimRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Christopher ThaiRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Olga LanchoRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Patricia Renck NunesRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Hayley AffrontiDepartment of Cancer Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Alexia Martínez de PazDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Steven Z JosefowiczDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Xiaoyang SuRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.
Kathryn E WellenDepartment of Cancer Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Daniel HerranzRutgers Cancer Institute, Rutgers University, New Brunswick, NJ.

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Rutgers Biotechnology Training ProgramT32GM135141 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI ANN M. STOCK, Martin L Yarmush · 2020 to 2026
$3.5M
The role of glutaminolysis as a therapeutic target in T-ALLR01CA236936 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI HERRANZ, DANIEL · 2019 to 2023
$1.8M
The role of pyruvate kinase as a therapeutic target in T-ALLR01CA285513 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Daniel Herranz · 2024 to 2026
$1.1M
An Orbitrap Tribrid mass spectrometer and nanoflow LC system to upgrade the proteomics facility at Rutgers-New Brunswick and Robert Wood Johnson Medical SchoolS10OD025140 · OD · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI LOBEL, PETER · 2019 to 2019
$921k
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA236936NCI NIH HHS R01 CA285513NIGMS NIH HHS T32 GM135141NIH HHS S10 OD025140
6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is a hematological malignancy in need of novel therapeutic approaches. Here, we identify ATP-citrate lyase (ACLY) as overexpressed in human T-ALL and as a promising therapeutic target for its treatment. To test the effects of ACLY in leukemia progression, we developed an isogenic model of NOTCH1-induced

Identifiers

PMID40453140
PMCPMC12067888

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.