Evidence map›Paper›PMID 40227585›Full record

ArticleCancers2025

Effect of Tasurgratinib as an Orally Available FGFR1-3 Inhibitor on Resistance to a CDK4/6 Inhibitor and Endocrine Therapy in ER

Satoshi Kawano, Sayo Fukushima, Kyoko Nishibata, Ryu Gejima, Saori Watanabe Miyano

Abstract read
In one paragraph

Article in Cancers, 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

5 authors.

Satoshi KawanoEisai Co., Ltd., Tsukuba 300-2635, Japan.ORCID 0009-0007-1712-6629
Sayo FukushimaEisai Co., Ltd., Tsukuba 300-2635, Japan.
Kyoko NishibataEisai Co., Ltd., Tsukuba 300-2635, Japan.
Ryu GejimaEisai Co., Ltd., Tsukuba 300-2635, Japan.
Saori Watanabe MiyanoEisai Co., Ltd., Tsukuba 300-2635, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFibroblast growth factor (FGF) signaling plays a crucial role in several cellular functions in cancer cells. Tasurgratinib, formerly known as E7090, is an orally available FGF receptor (FGFR)1-3 selective inhibitor. Here, we present the effects of tasurgratinib on the resistance to CDK4/6 inhibitors and endocrine therapy (ET) in a preclinical model.

methodsEstrogen receptor (ER)

resultsAmong five ER

conclusionsFGF signaling plays a role in resistance to CDK4/6 inhibitors and ET in ER

Indexed as

breast cancerCDK4/6 inhibitorendocrine therapyFGFRtasurgratinib

Identifiers

PMID40227585
PMCPMC11988047

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.