Evidence map›Paper›PMID 36683274›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2023

In silico identification and biological evaluation of a selective MAP4K4 inhibitor against pancreatic cancer.

Chao-Di Chang, Min-Wu Chao, Hsueh-Yun Lee, Yi-Ting Liu, Huang-Ju Tu, Ssu-Ting Lien, Tony Eight Lin, Tzu-Ying Sung, Shih-Chung Yen, Sing-Han Huang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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

12 authors at 6 institutions in 3 countries.

Chao-Di ChangPh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0002-1926-8344
Min-Wu ChaoSchool of Medicine, College of Medicine, National Sun Yat-sen University, Kaohsiung, Taiwan.ORCID 0000-0002-9122-3415
Hsueh-Yun LeePh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0001-6683-0726
Yi-Ting LiuSchool of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Huang-Ju TuGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0002-6866-7034
Ssu-Ting LienGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0001-6955-0703
Tony Eight LinGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0002-6267-0224
Tzu-Ying SungBiomedical Translation Research Center, Academia Sinica, Taipei, Taiwan.
Shih-Chung YenWarshel Institute for Computational Biology, The Chinese University of Hong Kong (Shenzhen), Shenzhen, Guangdong, People's Republic of China.ORCID 0000-0001-8596-0083
Sing-Han HuangGraphen Inc, New York, NY, USA.ORCID 0000-0003-0289-2260
Kai-Cheng HsuPh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0002-9022-6673
Shiow-Lin PanPh.D. Program in Drug Discovery and Development Industry, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0001-7449-3539
Taipei Medical University · TWAcademia Sinica · TWChinese University of Hong Kong, Shenzhen · CNMed Graph (United States) · USNational Sun Yat-sen University · TWWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibiting a specific target in cancer cells and reducing unwanted side effects has become a promising strategy in pancreatic cancer treatment. MAP4K4 is associated with pancreatic cancer development and correlates with poor clinical outcomes. By phosphorylating MKK4, proteins associated with cell apoptosis and survival are translated. Therefore, inhibiting MAP4K4 activity in pancreatic tumours is a new therapeutic strategy. Herein, we performed a structure-based virtual screening to identify MAP4K4 inhibitors and discovered the compound F389-0746 with a potent inhibition (IC

Indexed as

Antineoplastic AgentsPancreatic NeoplasmsProtein Kinase InhibitorsProtein Serine-Threonine KinasesCell Line, TumorComputer SimulationGemcitabineHumansIntracellular Signaling Peptides and ProteinsAntineoplastic AgentsGemcitabineIntracellular Signaling Peptides and ProteinsMAP4K4 protein, humanProtein Kinase InhibitorsProtein Serine-Threonine KinasesJNK signalling pathwaykinase inhibitorMAP4K4pancreatic cancerstructure-based virtual screening

Identifiers

PMID36683274
PMCPMC9873280
OpenAlexW4317780958

What OpenQuestion holds

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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.