Evidence map›Paper›PMID 41755877›Full record

ArticleJACS Au2026

A Small-Molecule SLD1121 Activates Wnt/β-Catenin Signaling and Promotes Hair Growth via Targeting the Wnt Coreceptor LRP6.

Qi Sun, Zhixian Lin, Yi Wang, Shujing Lei, Yuexuan Chen, Mingli Peng, Zijie Su, Jiaxing Song, Shanshan Liu, Jingang Liu and 2 more

Abstract read
In one paragraph

Article in JACS Au, 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

12 authors.

Qi SunDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Zhixian LinDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Yi WangShenzhen Key Lab of Functional Polymer, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, China.
Shujing LeiDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Yuexuan ChenDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Mingli PengDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Zijie SuDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Jiaxing SongDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Shanshan LiuDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.
Jingang LiuKey Laboratory for Advanced Materials, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China.ORCID https://orcid.org/0000-0002-5690-8881
Qianling ZhangShenzhen Key Lab of Functional Polymer, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, China.ORCID https://orcid.org/0000-0001-6942-3958
Desheng LuDepartment of Pharmacology, International Cancer Center, Shenzhen University Medical School, Shenzhen 518060, China.ORCID https://orcid.org/0000-0002-0314-5649

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LRP6 is a Wnt coreceptor and plays a key role in Wnt signal transduction. However, the molecular mechanism of LRP6 action in the Wnt signaling cascade has not been fully elucidated. In this study, a small molecule compound SLD1121 is synthesized and identified as a novel agonist of the Wnt/β-catenin signaling pathway. Our results showed that SLD1121 could enhance Wnt signaling through targeting LRP6. SLD1121 interacted with the intracellular domain of LRP6, stabilized LRP6, and accelerated its nuclear translocation. Moreover, SLD1121 promoted the association of LRP6 with β-catenin, or TCF4 or LEF1 in the nucleus, resulting in the expression of Wnt regulatory genes and stemness-associated genes. In a hair regeneration model of C57BL/6J mice, SLD1121 induced the transition of hair follicles from the telogen to anagen phase in the mouse hair growth cycle through the activation of Wnt/β-catenin signaling, resulting in enhanced hair growth of mice. Collectively, our results provide a novel insight into the molecular mechanism for the LRP6-mediated Wnt signaling cascade. By targeting LRP6, SLD1121 has the potential to be used as a therapeutic agent for alopecia.

Indexed as

AlopeciaLRP6SLD1121Wnt/β-catenin signaling

Identifiers

PMID41755877
PMCPMC12933300

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.