Evidence map›Paper›PMID 39641248›Full record

ArticleeLife2024

Synthesis and biological assessment of chalcone and pyrazoline derivatives as novel inhibitor for ELF3-MED23 interaction.

Soo-Yeon Hwang, Kyung-Hwa Jeon, Hwa-Jong Lee, Inhye Moon, Sehyun Jung, Seul-Ah Kim, Hyunji Jo, Seojeong Park, Misun Ahn, Soo-Yeon Kwak and 2 more

Abstract read
In one paragraph

Article in eLife, 2024. 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

12 authors.

Soo-Yeon Hwang *College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Kyung-Hwa Jeon *College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Hwa-Jong LeeCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Inhye MoonCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Sehyun JungCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Seul-Ah KimCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Hyunji JoCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Seojeong ParkCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Misun AhnCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.
Soo-Yeon KwakCollege of Pharmacy, CHA University, Pocheon, Republic of Korea.
Younghwa NaCollege of Pharmacy, CHA University, Pocheon, Republic of Korea.
Youngjoo KwonCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-6256-3042

Funding

Korea Basic Science Institute 2021R1A6C101A442National Research Foundation of Korea 2021M3E5E7024855National Research Foundation of Korea 2022R1A2C2092053National Research Foundation of Korea NRF-2018R1A5A2025286
6 · The paper itself

Abstract

HER2 overexpression significantly contributes to the aggressive nature and recurrent patterns observed in various solid tumors, notably gastric cancers. Trastuzumab, HER2-targeting monoclonal antibody drug, has shown considerable clinical success; however, readily emerging drug resistance emphasizes the pressing need for improved interventions in HER2-overexpressing cancers. To address this, we proposed targeting the protein-protein interaction (PPI) between ELF3 and MED23 as an alternative therapeutic approach to trastuzumab. In this study, we synthesized a total of 26 compounds consisting of 10 chalcones, 7 pyrazoline acetyl, and 9 pyrazoline propionyl derivatives, and evaluated their biological activity as potential ELF3-MED23 PPI inhibitors. Upon systematic analysis, candidate compound

Indexed as

ChalconesDNA-Binding ProteinsProto-Oncogene Proteins c-etsPyrazolesStomach NeoplasmsTranscription FactorsAnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationErb-b2 Receptor Tyrosine KinasesFemaleHumansMiceMice, NudeProtein BindingAntineoplastic AgentsChalconesDNA-Binding ProteinsELF3 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesProto-Oncogene Proteins c-etsPyrazolesTranscription Factors4-Methoxy-3-((3-methylbut-2-en-1-yl)oxy)benzaldehydebiochemistrychemical biologygastric cancerHER2-overexpressing cancershumanmedicineprotein-protein interaction inhibitortrastuzumab-resistance

Identifiers

PMID39641248
PMCPMC11623927

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.