Evidence map›Paper›PMID 32549194›Full record

ArticleCancers2020

Therapeutic Efficacy of ABN401, a Highly Potent and Selective MET Inhibitor, Based on Diagnostic Biomarker Test in

Jooseok Kim, Kyung Eui Park, Yoo-Seong Jeong, YeongMun Kim, Hayeon Park, Ji-Hye Nam, Kyungsoo Jung, Woo Sung Son, Hun Soon Jung, Jong-Hwa Lee and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

12 citing papers in PubMed, 12 citations in OpenAlex.

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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

19 authors at 6 institutions in 1 country.

Jooseok KimCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.ORCID 0000-0003-1653-574X
Kyung Eui ParkR&D Center, ABION Inc., Seoul 08394, Korea.
Yoo-Seong JeongCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.ORCID 0000-0002-4190-6525
YeongMun KimR&D Center, ABION Inc., Seoul 08394, Korea.
Hayeon ParkR&D Center, ABION Inc., Seoul 08394, Korea.
Ji-Hye NamDepartment of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul 08826, Korea.
Kyungsoo JungDepartment of Pathology & Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Woo Sung SonDepartment of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Gyeonggi-do 11160, Korea.ORCID 0000-0002-8319-9873
Hun Soon JungR&D Center, ABION Inc., Seoul 08394, Korea.
Jong-Hwa LeeDMPK Group, Korea Institute of Toxicology, Daejeon 305343, Korea.ORCID 0000-0002-5131-0514
Seong Hoon JeongLab of Pharmaceutical Engineering, College of Pharmacy, Dongguk University, Gyeonggi 10326, Korea.
Nam Ah KimR&D Center, ABION Inc., Seoul 08394, Korea.
Jae Du HaBio & Drug Discovery Division, Korea Research Institute of Chemical Technology, Yuseong-gu, Daejeon 34114, Korea.
Sung Yun ChoBio & Drug Discovery Division, Korea Research Institute of Chemical Technology, Yuseong-gu, Daejeon 34114, Korea.
Yoon-La ChoiDepartment of Pathology & Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Suk-Jae ChungCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.
Jun Young ChoiR&D Center, ABION Inc., Seoul 08394, Korea.
Sungyoul HongCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.
Young Kee ShinCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.ORCID 0000-0003-0896-718X
Seoul National University · KRDongguk University · KRKorea Research Institute of Chemical Technology · KRSamsung Medical Center · KRCHA University · KRKorea Institute of Toxicology · KR

Funding

Korea Drug Development Fund KDDF-20160803Ministry of Science, ICT and Future Planning 2016-935470Small and Medium Business Administration C0406256
6 · The paper itself

Abstract

The receptor tyrosine kinase c-MET regulates processes essential for tissue remodeling and mammalian development. The dysregulation of c-MET signaling plays a role in tumorigenesis. The aberrant activation of c-MET, such as that caused by gene amplification or mutations, is associated with many cancers. c-MET is therefore an attractive therapeutic target, and inhibitors are being tested in clinical trials. However, inappropriate patient selection criteria, such as low amplification or expression level cut-off values, have led to the failure of clinical trials. To include patients who respond to MET inhibitors, the selection criteria must include

Indexed as

c-METc-MET inhibitor (ABN401)diagnostic biomarkergastric cancernon-small cell lung cancer (NSCLC)patient-derived xenograft (PDX) modelspharmacodynamicspharmacokinetics

Identifiers

PMID32549194
PMCPMC7352216
OpenAlexW3035344440

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.