Evidence map›Paper›PMID 33879449›Full record

ArticleCancer discovery2021

RB/E2F1 as a Master Regulator of Cancer Cell Metabolism in Advanced Disease.

Amy C Mandigo, Wei Yuan, Kexin Xu, Peter Gallagher, Angel Pang, Yi Fang Guan, Ayesha A Shafi, Chellappagounder Thangavel, Beshara Sheehan, Denisa Bogdan and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.7field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 95 citations in OpenAlex.

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  18. KRASCell reports. Medicine · 2025
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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

25 authors at 4 institutions in 3 countries.

Amy C MandigoDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0003-4683-5268
Wei YuanThe Institute of Cancer Research, London, United Kingdom.
Kexin XuThe University of Texas Health Science Center at San Antonio, San Antonio, Texas.ORCID 0000-0002-2850-2083
Peter GallagherDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Angel PangSchool of Medical Sciences and Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
Yi Fang GuanSchool of Medical Sciences and Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
Ayesha A ShafiDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0003-0335-638X
Chellappagounder ThangavelDepartments of Urology, Medical Oncology and Radiation Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0002-5179-9364
Beshara SheehanThe Institute of Cancer Research, London, United Kingdom.
Denisa BogdanThe Institute of Cancer Research, London, United Kingdom.
Alec PaschalisThe Institute of Cancer Research, London, United Kingdom.
Jennifer J McCannDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Talya S LauferDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Nicolas GordonDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Irina A VasilevskayaDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0001-7550-5001
Emanuela DylgjeriDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Saswati N ChandDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0001-5625-0517
Matthew J SchiewerDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Josep Domingo-DomenechDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Robert B DenDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Jeff HolstDepartment of Dermatology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0002-0377-9318
Peter A McCueDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.
Johann S de BonoThe Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-2034-595X
Christopher McNairDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0003-3204-8482
Karen E KnudsenDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania. karen.knudsen@jefferson.edu.
Thomas Jefferson University · USRoyal Marsden NHS Foundation Trust · GBUNSW Sydney · AUThe University of Texas Health Science Center at San Antonio · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Andrew Chapman · 1995 to 2026
$94.8M
USP22 Function in Advanced Prostate CancerR01CA182569 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KNUDSEN, KAREN E, MCMAHON, STEVEN B. · 2015 to 2019
$2.4M
Determine the Microphthalmia Transcription Factor (MITF)-regulated cell rewiring mechanisms in lethal prostate cancerR01CA261925 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Josep Maria Domingo-Domenech · 2021 to 2026
$2.2M
Role of GATA2 signaling network in Lethal Prostate CancerR01CA207311 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DOMINGO-DOMENECH, JOSEP MARIA · 2016 to 2020
$2.2M
RB Function in Prostate Cancer ProgressionR01CA176401 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KNUDSEN, KAREN E · 2014 to 2018
$2.2M
Targeting Cell Cycle Alterations to Improve Treatment for Advanced Prostate CancerR01CA217329 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KELLY, WILLIAM K., MCNAIR, CHRISTOPHER MICHAEL · 2017 to 2021
$1.8M
Training Program in Cellular, Biochemical, and Molecular SciencesT32GM100836 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BENOVIC, JEFFREY L · 2012 to 2016
$809k
The Role of USP22 in Prostate Cancer Development and ProgressionF99CA212225 · NCI · THOMAS JEFFERSON UNIVERSITY · PI MCCANN, JENNIFER JONES · 2016 to 2017
$89k
NCI NIH HHS F99 CA212225NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA176401NCI NIH HHS R01 CA182569NCI NIH HHS R01 CA207311NCI NIH HHS R01 CA217329NCI NIH HHS R01 CA261925NIGMS NIH HHS T32 GM100836
6 · The paper itself

Abstract

Loss of the retinoblastoma (RB) tumor suppressor protein is a critical step in reprogramming biological networks that drive cancer progression, although mechanistic insight has been largely limited to the impact of RB loss on cell-cycle regulation. Here, isogenic modeling of RB loss identified disease stage-specific rewiring of E2F1 function, providing the first-in-field mapping of the E2F1 cistrome and transcriptome after RB loss across disease progression. Biochemical and functional assessment using both

Indexed as

AnimalsCell Line, TumorE2F1 Transcription FactorHumansMiceNeoplasm MetastasisRetinal NeoplasmsRetinoblastomaRetinoblastoma ProteinSignal TransductionXenograft Model Antitumor AssaysE2F1 protein, humanE2F1 Transcription FactorRetinoblastoma Protein

Identifiers

PMID33879449
PMCPMC8419081
OpenAlexW3154308842

What OpenQuestion holds

Textmetadata
LicenceTDM
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.