Evidence map›Paper›PMID 29142068›Full record

ArticleMolecular cancer therapeutics2018

Pharmacologic Inhibition of the Menin-MLL Interaction Leads to Transcriptional Repression of

Katarzyna Kempinska, Bhavna Malik, Dmitry Borkin, Szymon Klossowski, Shirish Shukla, Hongzhi Miao, Jingya Wang, Tomasz Cierpicki, Jolanta Grembecka

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

33 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Menin in Cancer.Genes · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Clinically Defined Mutations inCancer research communications · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Biomolecules · 2022
    Article
  20. 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

9 authors at 1 institution in 1 country.

Katarzyna Kempinska *Department of Pathology, University of Michigan, Ann Arbor, Michigan.
Bhavna Malik *Department of Pathology, University of Michigan, Ann Arbor, Michigan.
Dmitry BorkinDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Szymon KlossowskiDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Shirish ShuklaDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Hongzhi MiaoDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Jingya WangDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Tomasz CierpickiDepartment of Pathology, University of Michigan, Ann Arbor, Michigan. jolantag@umich.edu tomaszc@umich.edu.
Jolanta GrembeckaDepartment of Pathology, University of Michigan, Ann Arbor, Michigan. jolantag@umich.edu tomaszc@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Development of novel anti-leukemia agents targeting the menin-MLL interactionR01CA160467 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GREMBECKA, JOLANTA · 2011 to 2021
$3.4M
Targeting the MLL complex in Castration Resistant Prostate CancerR01CA200660 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, GREMBECKA, JOLANTA · 2016 to 2020
$1.9M
NCI NIH HHS R01 CA160467NCI NIH HHS R01 CA200660
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) accounts for approximately 85% of malignant liver tumors and results in 600,000 deaths each year, emphasizing the need for new therapies. Upregulation of menin was reported in HCC patients and high levels of menin correlate with poor patient prognosis. The protein-protein interaction between menin and histone methyltransferase mixed lineage leukemia 1 (MLL1) plays an important role in the development of HCC, implying that pharmacologic inhibition of this interaction could lead to new therapeutic strategy for the HCC patients. Here, we demonstrate that the menin-MLL inhibitor MI-503 shows antitumor activity in

Indexed as

AnimalsApoptosis Regulatory ProteinsCarcinoma, HepatocellularDisease Models, AnimalDNA-Binding ProteinsFemaleHumansLiver NeoplasmsMethylationMiceMice, NudeProtein BindingProteinsProto-Oncogene ProteinsRNA-Binding ProteinsTranscription FactorsApoptosis Regulatory ProteinsDNA-Binding ProteinsMEN1 protein, humanPEG10 protein, humanProteinsProto-Oncogene ProteinsRNA-Binding ProteinsTranscription Factors

Identifiers

PMID29142068
PMCPMC5752584
OpenAlexW2769932985

What OpenQuestion holds

Textmetadata
LicenceTDM
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.