Evidence map›Paper›PMID 41289612›Full record

ArticleBiofabrication2025

Therapeutic potential of TAS-115 in 3D breast cancer models.

Sendegul Yildirim, Momoka Nagamine, Myoung Hwan Kim, Amanda Becceneri, Nazmiye Celik, Ilayda Namli, Todd M Umstead, Zissis C Chroneos, Gamze Tanriover, Ibrahim T Ozbolat

Abstract read
In one paragraph

Article in Biofabrication, 2025. 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

10 authors.

Sendegul YildirimThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.
Momoka NagamineThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.
Myoung Hwan KimThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.
Amanda BecceneriThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.ORCID 0000-0001-5223-961X
Nazmiye CelikThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.
Ilayda NamliThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.ORCID 0000-0002-3776-5176
Todd M UmsteadDepartment of Pediatrics, Penn State University, Hershey, PA 17033, United States of America.ORCID 0009-0004-4112-711X
Zissis C ChroneosDepartment of Pediatrics, Penn State University, Hershey, PA 17033, United States of America.ORCID 0000-0002-9841-7917
Gamze TanrioverDepartment of Histology and Embryology, Akdeniz University, Antalya 07070, Türkiye.
Ibrahim T OzbolatThe Huck Institutes of Life Sciences, Penn State University, University Park, PA 16802, United States of America.ORCID 0000-0001-8328-4528

Funding

High-throughput Spheroid Bioprinting Technology for Scalable Fabrication of TissuesR01EB034566 · NIBIB · PENNSYLVANIA STATE UNIVERSITY, THE · PI Ibrahim Ozbolat · 2023 to 2026
$2.2M
NIBIB NIH HHS R01 EB034566
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is an aggressive subtype with limited treatment options. TAS-115, a multi-receptor tyrosine kinase inhibitor, has not previously been evaluated in TNBC. Here, we investigated its therapeutic effects alone and in combination with doxorubicin (DOXO), using three-dimensional heterotypic spheroid models, including free-standing, bioprinted static, and perfused systems. TAS-115 significantly reduced cell proliferation and viability, enhanced apoptosis, and suppressed c-mesenchymal-epithelial transition/hepatocyte growth factor and PI3K/Akt/mTOR signaling. Combined treatment with DOXO further amplified these effects. In perfused bioprinted models, TAS-115 markedly inhibited tumor cell migration, highlighting its potential to limit metastatic behavior. These findings identify TAS-115 as a promising therapeutic strategy for TNBC, either as a monotherapy or in combination with chemotherapy.

Indexed as

Antineoplastic AgentsModels, BiologicalTriple Negative Breast NeoplasmsApoptosisCell Line, TumorCell MovementCell ProliferationCell SurvivalDoxorubicinEpithelial-Mesenchymal TransitionFemaleHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionSpheroids, CellularAntineoplastic AgentsDoxorubicinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-akt3D modelsbioprintingbreast cancerheterotypic spheroids

Identifiers

PMID41289612
PMCPMC12683671

What Socratic 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 Socratic graph.