Evidence map›Paper›PMID 39133222›Full record

ReviewThe Journal of experimental medicine2024

The pathogenic role of retinoid nuclear receptor signaling in cancer and metabolic syndromes.

Mark Esposito, John K Amory, Yibin Kang

Abstract readReview
In one paragraph

Review in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Targeting the JAK/STAT signalling axis in cancer: chemopreventive potential of natural compounds with emerging focus on retinoids.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  8. Significance of Vitamins A and E in Cancer Progression and Prevention.International journal of molecular sciences · 2025
    Review
  9. Article
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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

3 authors.

Mark EspositoDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID 0000-0002-5724-4087
John K AmoryUniversity of Washington , Seattle, WA, USA.ORCID 0000-0002-7419-435X
Yibin KangDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID 0000-0002-1626-6730

Funding

ALDH1A1/A2 Inhibitors for Male ContraceptionR01HD098039 · NICHD · UNIVERSITY OF WASHINGTON · PI AMORY, JOHN K. · 2019 to 2023
$1.9M
Development of first-in-class antagonists of the retinoid pathway as novel oral immunotherapies for solid cancersR43CA278127 · NCI · KAYOTHERA INC. · PI ESPOSITO, MARK · 2023 to 2023
$398k
Development of first-in-class antagonists of the retinoid pathway as novel oral therapies for Type 2 DiabetesR43DK136420 · NIDDK · KAYOTHERA INC. · PI ESPOSITO, MARK · 2023 to 2023
$338k
American Cancer SocietyBreast Cancer Research FoundationBrewster FoundationEunice Kennedy Shriver National Institute of Health and Human ReproductionLudwig Cancer ResearchNCI NIH HHS R43 CA278127NCI NIH HHS R43DK136420New Jersey Health FoundationNICHD NIH HHS R01 HD098039NIDDK NIH HHS R43 DK136420NIH HHS R01HD098039Susan Komen Foundation
6 · The paper itself

Abstract

The retinoid nuclear receptor pathway, activated by the vitamin A metabolite retinoic acid, has been extensively investigated for over a century. This study has resulted in conflicting hypotheses about how the pathway regulates health and how it should be pharmaceutically manipulated. These disagreements arise from a fundamental contradiction: retinoid agonists offer clear benefits to select patients with rare bone growth disorders, acute promyelocytic leukemia, and some dermatologic diseases, yet therapeutic retinoid pathway activation frequently causes more harm than good, both through acute metabolic dysregulation and a delayed cancer-promoting effect. In this review, we discuss controlled clinical, mechanistic, and genetic data to suggest several disease settings where inhibition of the retinoid pathway may be a compelling therapeutic strategy, such as solid cancers or metabolic syndromes, and also caution against continued testing of retinoid agonists in cancer patients. Considerable evidence suggests a central role for retinoid regulation of immunity and metabolism, with therapeutic opportunities to antagonize retinoid signaling proposed in cancer, diabetes, and obesity.

Indexed as

Metabolic SyndromeNeoplasmsSignal TransductionAnimalsHumansReceptors, Retinoic AcidRetinoidsReceptors, Retinoic AcidRetinoids

Identifiers

PMID39133222
PMCPMC11318670

What OpenQuestion holds

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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.