Evidence map›Paper›PMID 41844686›Full record

ArticleScientific reports2026

Potential impact of nicorandil on the pharmacodynamics of anti-angiogenic agents.

Chen Pan, Kenji Onda, Kazuki Ebina, Mariko Kawakami, Mei Yokosawa, Toshihiko Hirano, Kenichi Suzuki

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Chen PanDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Kenji OndaDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan. knjond@toyaku.ac.jp.
Kazuki EbinaDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Mariko KawakamiDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Mei YokosawaDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Toshihiko HiranoDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.
Kenichi SuzukiDepartment of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, 192-0392, Japan.

Funding

China Academy of Chinese Medical Sciences Foundation ZZ15- YQ-046JSPS KAKENHI JP19K07207National Natural Science Foundation of China 82304861
6 · The paper itself

Abstract

Anti-angiogenic agents are widely used to treat solid tumors. We previously demonstrated that nicorandil, an angina pectoris medication, counteracted the effects of bevacizumab in a human mini-tumor model. To further elucidate the potential pharmacodynamic interactions and possible clinical implications, we conducted an integrative investigation combining an in vivo mouse model and a large-scale analysis of clinical adverse event reports. In tumor-bearing nude mice, aflibercept treatment markedly increased systemic blood pressure and substantially reduced tumor volume, whereas co-administration of nicorandil mitigated both responses. Additionally, an analysis of the Unites States Food and Drug Administration Adverse Event Reporting System data (FAERS [JAPIC AERS]) was conducted. Concomitant use of anti-angiogenic agents and nicorandil was infrequently reported; therefore, this data must be interpreted with caution. However, the tendency of reduced reporting odds ratios of hypertension and proteinuria and instances of hypotension were documented. Collectively, these findings suggest that nicorandil may counteract the pharmacodynamic effects of anti-angiogenic agents when administered concurrently. Therefore, further clinical validation is warranted.

Indexed as

Angiogenesis InhibitorsNicorandilAnimalsBlood PressureDrug InteractionsFemaleHumansHypertensionMaleMiceMice, NudeReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsXenograft Model Antitumor AssaysafliberceptAngiogenesis InhibitorsNicorandilReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsAnti-angiogenic agentsAntitumor effectDrug–drug interactionHypertensionNicorandil

Identifiers

PMID41844686
PMCPMC13128807

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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.