Evidence map›Paper›PMID 40429734›Full record

ArticleInternational journal of molecular sciences2025

A High-Throughput Cell-Based Luciferase Reporter Assay for Identifying Inhibitors of ASGR1.

Lingmin Gan, Haoyu Zou, Zhaoqi Yang, Juntao Wang, Yunzhi Sheng, Pengfei Du, Shikun Zhang, Zili Feng

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Lingmin GanSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.
Haoyu ZouAcademy of Military Medical Sciences, Beijing 100850, China.ORCID 0000-0003-0778-4920
Zhaoqi YangSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.
Juntao WangSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.ORCID 0009-0009-2817-1526
Yunzhi ShengSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.
Pengfei DuSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.ORCID 0009-0005-3436-5192
Shikun ZhangAcademy of Military Medical Sciences, Beijing 100850, China.
Zili FengSchool of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723099, China.

Funding

National Natural Science Foundation of China 82204277
6 · The paper itself

Abstract

The asialoglycoprotein receptor 1 (ASGR1) represents a highly promising target for drug development, with its expression regulation closely linked to various diseases. Consequently, research concentrating on targeted therapies against ASGR1 holds significant importance in devising effective treatment strategies. In this study, we utilized the CRISPR-Knockin technology to insert a firely luciferase reporter gene downstream of exon 9 of the ASGR1 gene in HepG2 cell line. This modification enables the expression level of luciferase to be directly proportional to the activity intensity of the ASGR1 protein. We successfully established a drug screening and evaluation model for ASGR1 and employed it for high-throughput screening of potential inhibitors from a microbial molecular metabolite library. After our screening process, several promising candidates were identified as potential ASGR1 inhibitors. Western blotting experiment was conducted to validate the efficacy of our drug screening model, thereby providing a solid experimental foundation for the development of novel targeted therapeutics targeting ASGR1.

Indexed as

Asialoglycoprotein ReceptorGenes, ReporterHigh-Throughput Screening AssaysLuciferasesDrug Evaluation, PreclinicalHep G2 CellsHumansAsialoglycoprotein ReceptorLuciferasesASGR1Crispr-Knockinfirely luciferasehigh-throughput drug screening

Identifiers

PMID40429734
PMCPMC12111582

What OpenQuestion holds

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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.