Evidence map›Paper›PMID 36497445›Full record

ArticleCancers2022

The Microtubule Destabilizer Eribulin Synergizes with STING Agonists to Promote Antitumor Efficacy in Triple-Negative Breast Cancer Models.

Leila Takahashi-Ruiz, Charles S Fermaintt, Nancy J Wilkinson, Peter Y W Chan, Susan L Mooberry, April L Risinger

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. cGAS/STING-Independent Induction of Type I Interferon by Inhibitors of the Histone Methylase KDM5B.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 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

6 authors at 1 institution in 1 country.

Leila Takahashi-RuizDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0003-1814-6465
Charles S FermainttDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0001-8140-5461
Nancy J WilkinsonDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.
Peter Y W ChanDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0002-3498-6301
Susan L MooberryDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0001-8575-2516
April L RisingerDepartment of Pharmacology, University of Texas Health Science Center San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0002-4363-3268
The University of Texas Health Science Center at San Antonio · US

Funding

San Antonio Biomedical Education and ResearchK12GM111726 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LECHLEITER, JAMES D, OYAJOBI, BABATUNDE OLUKAYODE · 2015 to 2024
$7.6M
Recruiting and Retaining URM StudentsR25GM095480 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI OYAJOBI, BABATUNDE OLUKAYODE, WEISS, DAVID S · 2011 to 2021
$3.4M
NRSA Training Core (TL1)TL1TR002647 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA, FREI, CHRISTOPHER R. · 2018 to 2022
$1.8M
Eisai Inc 167636NIGMS NIH HHS K12 GM111726NIH HHS 5R25GM095480NIH HHS GM111726NIH HHS TR002647
6 · The paper itself

Abstract

Eribulin is a microtubule destabilizer used in the treatment of triple-negative breast cancer (TNBC). Eribulin and other microtubule targeted drugs, such as the taxanes, have shared antimitotic effects, but differ in their mechanism of microtubule disruption, leading to diverse effects on cellular signaling and trafficking. Herein, we demonstrate that eribulin is unique from paclitaxel in its ability to enhance expression of the immunogenic cytokine interferon beta (IFNβ) in combination with STING agonists in both immune cells and TNBC models, including profound synergism with ADU-S100 and E7766, which are currently undergoing clinical trials. The mechanism by which eribulin enhances STING signaling is downstream of microtubule disruption and independent of the eribulin-dependent release of mitochondrial DNA. Eribulin did not override the requirement of ER exit for STING activation and did not inhibit subsequent STING degradation; however, eribulin significantly enhanced IRF3 phosphorylation and IFNβ production downstream of the RNA sensing pathway that converges on this transcription factor. Additionally, we found that eribulin enhanced the population of activated CD4

Indexed as

cancer immunotherapycGAS-STINGeribulinIFNβmicrotubule destabilizersmicrotubule-targeting agentstriple-negative breast cancertype I interferons

Identifiers

PMID36497445
PMCPMC9740651
OpenAlexW4311108317

What OpenQuestion holds

Textmetadata
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.