Evidence map›Paper›PMID 38815134›Full record

ArticleJCI insight2024

Drug screening in human physiologic medium identifies uric acid as an inhibitor of rigosertib efficacy.

Vipin Rawat, Patrick DeLear, Prarthana Prashanth, Mete Emir Ozgurses, Anteneh Tebeje, Philippa A Burns, Kelly O Conger, Christopher Solís, Yasir Hasnain, Anna Novikova and 9 more

Abstract read
In one paragraph

Article in JCI insight, 2024. 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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Vipin RawatDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Patrick DeLearDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Prarthana PrashanthDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Mete Emir OzgursesDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Anteneh TebejeDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Philippa A BurnsDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Kelly O CongerDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Christopher SolísDepartment of Nutrition and Integrative Physiology, Florida State University, Tallahassee, Florida, USA.
Yasir HasnainDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Anna NovikovaDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.
Jennifer E EndressMeyer Cancer Center, Weill Cornell Medicine, New York, New York, USA.
Paloma González-SánchezDepartment of Metabolism and Physiology, Moffitt Cancer Center, Tampa, Florida, USA.
Wentao DongDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Greg StephanopoulosDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Gina M DeNicolaDepartment of Metabolism and Physiology, Moffitt Cancer Center, Tampa, Florida, USA.
Isaac S HarrisDepartment of Biomedical Genetics, Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, New York, USA.
David SeptDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Frank M MasonDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Jonathan L ColoffDepartment of Physiology and Biophysics, University of Illinois College of Medicine, University of Illinois Cancer Center, Chicago, Illinois, USA.

Funding

UCSD PRIDE Faculty Development Program in Cardiovascular SciencesR25HL145817 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Robert Scott Ross, Joann Trejo · 2019 to 2026
$3.3M
Investigation of NRF2-Dependent Metabolic LiabilitiesR37CA230042 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DENICOLA, GINA MARIE · 2018 to 2024
$2.8M
Targeting Serine Auxotrophy in Luminal Breast CancerR37CA251216 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Jonathan L. Coloff · 2021 to 2026
$2.1M
Post-translational mechanisms of cardiac adaptation during unloadingR00HL151825 · NHLBI · FLORIDA STATE UNIVERSITY · PI SOLIS OCAMPO, CHRISTOPHER · 2023 to 2025
$747k
Identifying Proliferation-Independent Metabolic Vulnerabilities in CancerK22CA215828 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI COLOFF, JONATHAN L. · 2018 to 2020
$564k
NCI NIH HHS K22 CA215828NCI NIH HHS R37 CA230042NCI NIH HHS R37 CA251216NHLBI NIH HHS R00 HL151825NHLBI NIH HHS R25 HL145817
6 · The paper itself

Abstract

The nonphysiological nutrient levels found in traditional culture media have been shown to affect numerous aspects of cancer cell physiology, including how cells respond to certain therapeutic agents. Here, we comprehensively evaluated how physiological nutrient levels affect therapeutic response by performing drug screening in human plasma-like medium. We observed dramatic nutrient-dependent changes in sensitivity to a variety of FDA-approved and clinically trialed compounds, including rigosertib, an experimental cancer therapeutic that recently failed in phase III clinical trials. Mechanistically, we found that the ability of rigosertib to destabilize microtubules is strongly inhibited by the purine metabolism end product uric acid, which is uniquely abundant in humans relative to traditional in vitro and in vivo cancer models. These results demonstrate the broad and dramatic effects nutrient levels can have on drug response and how incorporation of human-specific physiological nutrient medium might help identify compounds whose efficacy could be influenced in humans.

Indexed as

GlycineSulfonesUric AcidAntineoplastic AgentsCell Line, TumorCulture MediaDrug Evaluation, PreclinicalHumansAntineoplastic AgentsCulture MediaGlycineON 01910SulfonesUric AcidCancerCell biologyCytoskeletonDrug screensOncology

Identifiers

PMID38815134
PMCPMC11383364

What OpenQuestion holds

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Registered trials

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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.