Evidence map›Paper›PMID 31577956›Full record

ArticleCell reports2019

A Small-Molecule Pan-Id Antagonist Inhibits Pathologic Ocular Neovascularization.

Paulina M Wojnarowicz, Raquel Lima E Silva, Masayuki Ohnaka, Sang Bae Lee, Yvette Chin, Anita Kulukian, Sung-Hee Chang, Bina Desai, Marta Garcia Escolano, Riddhi Shah and 23 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  4. The role of Id genes on pulmonary hypertension development in left heart failure.American heart journal plus : cardiology research and practice · 2026
    Article
  5. Article
  6. Science advances · 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

33 authors at 8 institutions in 1 country.

Paulina M WojnarowiczCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Raquel Lima E SilvaDepartments of Ophthalmology and Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Masayuki OhnakaDepartments of Ophthalmology and Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Sang Bae LeeInstitute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
Yvette ChinCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Anita KulukianCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Sung-Hee ChangDepartment of Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
Bina DesaiCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Marta Garcia EscolanoCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Riddhi ShahCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Marta Garcia-CaoCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Sijia XuCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Rashmi KadamCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Yehuda GoldgurStructural Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Meredith A MillerStructural Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Ouathek OuerfelliOrganic Synthesis Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Guangli YangOrganic Synthesis Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Tsutomu ArakawaAlliance Protein Laboratories, a Division of KBI Biopharma, San Diego, CA 92121, USA.
Steven K AlbaneseComputational Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
William A GarlandTosk, Inc., Mountain View, CA 94043, USA.
Glenn StollerOphthalmic Consultants of Long Island, Lynbrook, NY 11563, USA.
Jaideep ChaudharyCenter for Cancer Research and Therapeutic Development, Clark Atlanta University, Atlanta, GA 30314, USA.
Larry NortonEvelyn H. Lauder Breast Center, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Rajesh Kumar SoniProteomics & Microchemistry Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
John PhilipProteomics & Microchemistry Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Ronald C HendricksonProteomics & Microchemistry Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Antonio IavaroneDepartment of Neurology, Department of Pathology, Institute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
Andrew J DannenbergDepartment of Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
John D ChoderaComputational Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Nikola PavletichStructural Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Anna LasorellaDepartment of Pediatrics, Department of Pathology, Institute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
Peter A CampochiaroDepartments of Ophthalmology and Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Robert BenezraCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: benezrar@mskcc.org.
Memorial Sloan Kettering Cancer Center · USColumbia University Irving Medical Center · USJohns Hopkins University · USCornell University · USAlliance Protein Laboratories (United States) · USCenter for Cancer Research · USOphthalmic Consultants of Long Island · USTosk (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
The Role of Id Proteins in Breast TumorigenesisP01CA094060 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI NORTON, LARRY · 2002 to 2018
$39.4M
The role of Id proteins in tumor development and angiogenesis in the brainR01CA101644 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LASORELLA, ANNA · 2003 to 2013
$3.5M
Mechanisms of ID2 regulation in gliomaR01CA239721 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LASORELLA, ANNA · 2019 to 2023
$1.8M
The Ureb-1 ubiquitin ligase in neural stem cells and cancerR01CA131126 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LASORELLA, ANNA · 2008 to 2012
$1.6M
LTQ-ORBITRAP VELOS Tandem Mass SpectrometerS10OD010598 · OD · SLOAN-KETTERING INST CAN RESEARCH · PI HENDRICKSON, RONALD CHARLES · 2012 to 2012
$460k
Studies in Mice to Improve Efficacy/Safety of Paclitaxel/Docetaxel with an Anti-IR43CA150448 · NCI · ANGIOGENEX · PI GARLAND, WILLIAM A. · 2010 to 2010
$163k
NCI NIH HHS P01 CA094060NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA101644NCI NIH HHS R01 CA131126NCI NIH HHS R01 CA239721NCI NIH HHS R43 CA150448NIH HHS S10 OD010598
6 · The paper itself

Abstract

Id helix-loop-helix (HLH) proteins (Id1-4) bind E protein bHLH transcription factors, preventing them from forming active transcription complexes that drive changes in cell states. Id proteins are primarily expressed during development to inhibit differentiation, but they become re-expressed in adult tissues in diseases of the vasculature and cancer. We show that the genetic loss of Id1/Id3 reduces ocular neovascularization in mouse models of wet age-related macular degeneration (AMD) and retinopathy of prematurity (ROP). An in silico screen identifies AGX51, a small-molecule Id antagonist. AGX51 inhibits the Id1-E47 interaction, leading to ubiquitin-mediated degradation of Ids, cell growth arrest, and reduced viability. AGX51 is well-tolerated in mice and phenocopies the genetic loss of Id expression in AMD and ROP models by inhibiting retinal neovascularization. Thus, AGX51 is a first-in-class compound that antagonizes an interaction formerly considered undruggable and that may have utility in the management of multiple diseases.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell LineCell Line, TumorCell ProliferationFemaleHCT116 CellsHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsInhibitor of Differentiation Protein 1MaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, NudeBasic Helix-Loop-Helix ProteinsInhibitor of Differentiation Protein 1Small Molecule LibrariesangiogenesisId proteinsmacular degenerationprotein-protein interactionsretinopathy of prematurity

Identifiers

PMID31577956
PMCPMC6896334
OpenAlexW2979187945

What OpenQuestion holds

Textmetadata
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.