Evidence map›Paper›PMID 25852826›Full record

ArticleClinical and translational medicine2015

MELK-a conserved kinase: functions, signaling, cancer, and controversy.

Ranjit Ganguly, Ahmed Mohyeldin, Jordyn Thiel, Harley I Kornblum, Monique Beullens, Ichiro Nakano

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

77 citing papers in PubMed, 121 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Targeting MELK in tumor cells and tumor microenvironment: from function and mechanism to therapeutic application.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. PCAT19: the role in cancer pathogenesis and beyond.Frontiers in cell and developmental biology · 2024
    Review
  15. Article
  16. Review
  17. Pharmacological reviews · 2023
    Review
  18. Article
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 1 country.

Ranjit GangulyDepartment of Neurological Surgery, The Ohio State University, 385 Wiseman Hall, 410 W 12th St., 43210 Columbus, OH USA.
Ahmed MohyeldinDepartment of Neurological Surgery, The Ohio State University, 385 Wiseman Hall, 410 W 12th St., 43210 Columbus, OH USA.
Jordyn ThielDepartment of Neurological Surgery, The Ohio State University, 385 Wiseman Hall, 410 W 12th St., 43210 Columbus, OH USA.
Harley I KornblumSemel Institute for Psychiatry and Human Behavior and the Jonsson Comprehensive Cancer Center, UCLA School of Medicine, Columbus, USA.
Monique BeullensLaboratory of Biosignaling & Therapeutics Department of Cellular and Molecular Medicine Campus Gasthuisberg, Gasthuisberg, Belgium.
Ichiro NakanoDepartment of Neurological Surgery, The Ohio State University, 385 Wiseman Hall, 410 W 12th St., 43210 Columbus, OH USA ; The James Comprehensive Cancer Center, The Ohio State University, Columbus, USA.
The Ohio State University · USNeurological Surgery · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USUCLA Jonsson Comprehensive Cancer Center

Funding

The Tumor Microenvironmental Barrier to Effective Viral OncolysisP01CA163205 · NCI · OHIO STATE UNIVERSITY · PI MICHAEL A CALIGIURI · 2013 to 2026
$26.0M
Targeting MELK-mediated EZH2 signaling in glioma stem cellsR01NS083767 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEE, JEONGWU, NAKANO, ICHIRO · 2013 to 2017
$1.3M
NCI NIH HHS P01 CA163205NINDS NIH HHS R01 NS083767
6 · The paper itself

Abstract

Maternal embryonic leucine zipper kinase (MELK) is a highly conserved serine/threonine kinase initially found to be expressed in a wide range of early embryonic cellular stages, and as a result has been implicated in embryogenesis and cell cycle control. Recent evidence has identified a broader spectrum of tissue expression pattern for this kinase than previously appreciated. MELK is expressed in several human cancers and stem cell populations. Unique spatial and temporal patterns of expression within these tissues suggest that MELK plays a prominent role in cell cycle control, cell proliferation, apoptosis, cell migration, cell renewal, embryogenesis, oncogenesis, and cancer treatment resistance and recurrence. These findings have important implications for our understanding of development, disease, and cancer therapeutics. Furthermore understanding MELK signaling may elucidate an added dimension of stem cell control.

Indexed as

CancerCancer-initiating cellsCancer therapeuticsDevelopmentGlioblastomaGlioma-initiating cellsMaternal embryonic leucine zipper kinaseMELKMitotic kinase

Identifiers

PMID25852826
PMCPMC4385133
OpenAlexW2148614367

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.