Evidence map›Paper›PMID 25721045›Full record

ArticleCell death and differentiation2015

The LIM-only transcription factor LMO2 determines tumorigenic and angiogenic traits in glioma stem cells.

S-H Kim, E-J Kim, M Hitomi, S-Y Oh, X Jin, H-M Jeon, S Beck, X Jin, J-K Kim, C G Park and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Analysis of the effect of LMO2 on indicating CD8Biochemistry and biophysics reports · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
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  13. Article
  14. Article
  15. Review
  16. Bivalent Genes Targeting of Glioma Heterogeneity and Plasticity.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Decreased Expression ofInternational journal of molecular sciences · 2020
    Article
  19. Review
  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

19 authors at 8 institutions in 2 countries.

S-H Kim1] School of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea [2] Department of Neurological Surgery, The Ohio State University, Columbus, OH 43210, USA.
E-J KimSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
M HitomiDepartment of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
S-Y OhSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
X JinDepartment of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
H-M JeonSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
S BeckDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712, USA.
X JinSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
J-K KimSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
C G ParkSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
S-Y ChangSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
J YinSpecific Organs Cancer Branch, Research Institute and Hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
T KimDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Y-J JeonDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210, USA.
J SongDepartment of Neurological Surgery, The Ohio State University, Columbus, OH 43210, USA.
Y C LimDepartment of Otorhinolaryngology-Head and Neck Surgery, Research Institute of Medical Science, Konkuk University School of Medicine, Seoul 143-752, Republic of Korea.
J D Lathia1] Department of Cellular and Molecular Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA [2] Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine, Cleveland, OH 44195, USA [3] Case Comprehensive Cancer Center, Cleveland, OH 44195, USA.
I Nakano1] Department of Neurological Surgery, The Ohio State University, Columbus, OH 43210, USA [2] James Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
H KimSchool of Life Sciences and Biotechnology and Institute of Life Science and Natural Resources, Korea University, Seoul 136-713, Republic of Korea.
Korea University · KRCleveland Clinic Lerner College of Medicine · USThe Ohio State University · USKonkuk University · KRNational Cancer Center · KRThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USThe University of Texas at Austin · USThe University of Texas MD Anderson Cancer Center · US

Funding

The Tumor Microenvironmental Barrier to Effective Viral OncolysisP01CA163205 · NCI · OHIO STATE UNIVERSITY · PI MICHAEL A CALIGIURI · 2013 to 2026
$26.0M
Metabolism Informs Intertumoral & Intratumoral HeterogeneityR01NS087913 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NAKANO, ICHIRO, RICH, JEREMY N · 2014 to 2018
$2.0M
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
Determination of Musashi1/CD44v6 signaling in mesenchymal glioma stem cellsR21CA175875 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NAKANO, ICHIRO, PENALVA, LUIZ OTAVIO · 2014 to 2015
$377k
NCI NIH HHS P01 CA163205NCI NIH HHS R21 CA175875NINDS NIH HHS R01 NS083767NINDS NIH HHS R01 NS087913
6 · The paper itself

Abstract

Glioblastomas (GBMs) maintain their cellular heterogeneity with glioma stem cells (GSCs) producing a variety of tumor cell types. Here we interrogated the oncogenic roles of Lim domain only 2 (LMO2) in GBM and GSCs in mice and human. High expression of LMO2 was found in human patient-derived GSCs compared with the differentiated progeny cells. LMO2 is required for GSC proliferation both in vitro and in vivo, as shRNA-mediated LMO2 silencing attenuated tumor growth derived from human GSCs. Further, LMO2 is sufficient to induce stem cell characteristics (stemness) in mouse premalignant astrocytes, as forced LMO2 expression facilitated in vitro and in vivo growth of astrocytes derived from Ink4a/Arf null mice and acquisition of GSC phenotypes. A subset of mouse and human GSCs converted into vascular endothelial-like tumor cells both in vitro and in vivo, which phenotype was attenuated by LMO2 silencing and promoted by LMO2 overexpression. Mechanistically, the action of LMO2 for induction of glioma stemness is mediated by transcriptional regulation of Jagged1 resulting in activation of the Notch pathway, whereas LMO2 directly occupies the promoter regions of the VE-cadherin gene for a gain of endothelial cellular phenotype. Subsequently, selective ablation of human GSC-derived VE-cadherin-expressing cells attenuated vascular formation in mouse intracranial tumors, thereby significantly prolonging mouse survival. Clinically, LMO2 expression was elevated in GBM tissues and inversely correlated with prognosis of GBM patients. Taken together, our findings describe novel dual roles of LMO2 to induce tumorigenesis and angiogenesis, and provide potential therapeutic targets in GBMs.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsApoptosisBrain NeoplasmsCell Line, TumorGlioblastomaHeterograftsHumansHuman Umbilical Vein Endothelial CellsLIM Domain ProteinsMiceMice, Inbred BALB CMice, NudeNeoplastic Stem CellsNeovascularization, PathologicProto-Oncogene ProteinsAdaptor Proteins, Signal TransducingLIM Domain ProteinsLMO2 protein, humanProto-Oncogene Proteins

Identifiers

PMID25721045
PMCPMC4532780
OpenAlexW2162621700

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.