Evidence map›Paper›PMID 41830514›Full record

ArticleThe FEBS journal2026

Spatiotemporal dynamics of β-arrestin-mediated Src activation in 5-HT7 receptor signaling pathway.

Hyunbin Kim, Yong Woo Lee, Huimin Lee, Eunseo Park, Jieon Lee, Hae Nim Lee, Kyeong-Man Kim, Hyunah Choo, Jihye Seong

Abstract read
In one paragraph

Article in The FEBS journal, 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

9 authors.

Hyunbin KimDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yong Woo LeeBrain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Huimin LeeDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Eunseo ParkMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Jieon LeeNew Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, Republic of Korea.
Hae Nim LeeDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Kyeong-Man KimCollege of Pharmacy, Chonnam National University, Gwangju, Republic of Korea.
Hyunah ChooMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-3545-2678
Jihye SeongDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8450-3315

Funding

Korea Health Industry Development Institute (KHIDI) RS-2025-25459221Korea Institute of Science and Technology (KIST) Institutional Program 2E33791; 2V10650National Research Foundation of Korea RS-2023-00227950National Research Foundation of Korea RS-2024-00338426National Research Foundation of Korea RS-2024-004073National Research Foundation of Korea RS-2025-00558008
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) initiate G protein-mediated signaling pathways upon ligand binding and are desensitized via β-arrestin-dependent internalization. However, emerging evidence indicates that β-arrestin also mediates G protein-independent signaling pathways that lead to distinct cellular responses. This signaling complexity has led to the development of GPCR-biased ligands that selectively modulate either G protein- or β-arrestin-dependent pathways for drug discovery, offering precise control of cellular processes with minimal side effects. We have developed biased ligands for the 5-hydroxytryptamine receptor subtype 7 (5-HT

Indexed as

beta-ArrestinsReceptors, SerotoninSignal Transductionsrc-Family KinasesAnimalsHEK293 CellsHumansLigandsMiceProto-Oncogene Masbeta-ArrestinsLigandsMAS1 protein, humanProto-Oncogene MasReceptors, Serotoninserotonin 7 receptorsrc-Family Kinases5‐HT7GPCR‐biased signalingserotoninsrcβ‐arrestin

Identifiers

PMID41830514
PMCPMC13489520

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Registered trials

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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.