Evidence map›Paper›PMID 41929148›Full record

ArticlebioRxiv : the preprint server for biology2026

Comprehensive analysis of TEAD inhibition in meningioma identifies MEK and mTOR inhibition as effective combination therapies against resistant lines.

Dylan J Keiser, Meghan S Buddy, Solmaz Mojarad-Jabali, Qing Li, Missia Kohler-Skinner, Abigail G Parrish, David Gillespie, David Nix, Sheri Holmen, Howard Colman and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Dylan J KeiserHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Meghan S BuddyHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Solmaz Mojarad-JabaliHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Qing LiHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Missia Kohler-SkinnerHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Abigail G ParrishHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, 98109, USA.ORCID 0009-0009-9183-7925
David GillespieHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
David NixHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Sheri HolmenHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Howard ColmanHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
William CouldwellDepartment of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, UT 84112, USA.
Randy JensenHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.
Frank SzulzewskyHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.ORCID 0000-0001-5710-9590

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

Meningiomas are the most common primary central nervous system tumors in adults, posing a significant burden to society. Although a large percentage of lower-grade meningiomas are curable by surgery or radiation alone, high-grade and a subset of low-grade meningiomas demonstrate recurrences and complications from treatment. Systemic therapies for meningioma remain ineffective, and no targeted treatments are approved. Despite the central role of YAP1/TAZ-TEAD signaling in NF2-deficient/mutant tumors, no studies have systematically examined TEAD inhibition across molecularly defined meningioma subtypes or investigated mechanisms of resistance in this disease. We have recently shown that YAP1/TAZ signaling is an oncogenic driver of meningioma. Here, using established and patient-derived meningioma cell lines, we demonstrate that genetic ablation of YAP1/TAZ suppresses growth in both NF2 mutant and NF2 wild type cell lines, establishing YAP1/TAZ-TEAD signaling as a shared oncogenic dependency. Pharmacologic TEAD inhibition suppressed growth of benign NF2 mutant and a subset of higher-grade NF2 mutant meningiomas, whereas NF2 wild type meningiomas were generally more resistant. RNA-Seq and Western Blot analysis identified compensatory activation of MEK-ERK, mTOR-S6, and FAK signaling in resistant lines exhibit. Importantly, co-targeting these pathways was able to overcome resistance to TEADi and was superior to MEK/mTOR/FAK inhibition alone. These studies provide a compelling proof-of-concept that TEADi represents a novel therapeutic vulnerability in meningioma and reveal adaptive signaling responses that can be therapeutically exploited.

Identifiers

PMID41929148
PMCPMC13041971

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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.