Evidence map›Paper›PMID 29199006›Full record

ArticleCancer letters2018

LB-100, a novel Protein Phosphatase 2A (PP2A) inhibitor, sensitizes malignant meningioma cells to the therapeutic effects of radiation.

Winson S Ho, Saman Sizdahkhani, Shuyu Hao, Hua Song, Ashlee Seldomridge, Anita Tandle, Dragan Maric, Tamalee Kramp, Rongze Lu, John D Heiss and 4 more

Abstract read
In one paragraph

Article in Cancer letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Targeting PP2A in cancer: an underrated option.Journal of experimental & clinical cancer research : CR · 2025
    Review
  6. Review
  7. Article
  8. Co-evolution of glioma and immune microenvironment.Journal for immunotherapy of cancer · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Targeting PP2A for cancer therapeutic modulation.Cancer biology & medicine · 2022
    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

14 authors at 4 institutions in 1 country.

Winson S HoSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA; Department of Neurosurgery, University of Virginia, Charlottesville, VA, USA.
Saman SizdahkhaniSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Shuyu HaoNeuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Hua SongNeuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Ashlee SeldomridgeNeuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Anita TandleRadiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Dragan MaricFlow Cytometry Core, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Tamalee KrampRadiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Rongze LuAbbVie Biotherapeutics, Redwood City, CA, USA.
John D HeissSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Kevin CamphausenRadiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mark R GilbertNeuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Zhengping ZhuangSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA; Neuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: zhengping.zhuang@nih.gov.
Deric M ParkNeuro-oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: deric.park@nih.gov.
National Cancer Institute · USNational Institutes of Health · USAbbVie (United States) · USUniversity of Virginia · US

Funding

Brain Tumor Clinical and Clinical Research Program (Clinical Support Services)ZIDBC011642 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI OZER, BYRAM · 2015 to 2025
$23.4M
The Synergy Between Radiotherapy and Molecularly Targeted AgentsZIASC010373 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI CAMPHAUSEN, KEVIN · 2009 to 2025
$22.2M
Molecular Pathogenesis of NeoplasiaZIANS003052 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI HEISS, JOHN · 2009 to 2025
$20.7M
Neurooncology of Benign Central and Peripheral Nervous System TumorsZIANS003132 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI CHITTIBOINA, PRASHANT · 2012 to 2025
$7.8M
Howard Hughes Medical InstituteIntramural NIH HHS Z99 NS999999
6 · The paper itself

Abstract

Atypical and anaplastic meningiomas (AAM) represent 20% of all meningiomas. They are associated with poor outcomes due to their tendency to recur. While surgery and radiation (RT) are first line therapy, no effective systemic medical treatment has been identified. Protein phosphatase 2A (PP2A) is a ubiquitously expressed serine/threonine phosphatase involved in cell cycle regulation and DNA repair. Here, we examined radiosensitizing effects of LB-100, a novel inhibitor of PP2A against AAM as a novel treatment strategy. Three human-derived immortalized meningioma cell lines, IOMM-LEE, GAR, and CH-157, were used to investigate the radio-sensitizing potential of LB-100 in AAM. Survival fraction by clonogenic assay, immunofluorescence, cell cycle analysis and protein expression were evaluated in vitro. The antitumor effects of combining LB-100 with RT were verified in vivo by using intracranial orthotopic xenograft mouse model. Pharmacologic PP2A inhibition with LB-100 prior to RT enhanced the radiosensitivity of meningioma cells and reduced survival fraction in clonogenic assays. LB-100 increased DNA double-strand breakage (measured by γ-H2AX), mitotic catastrophe cell death, and G2/M cell cycle arrest in irradiated meningioma cells. Also, LB-100 decreased activation of STAT3 and expression of its downstream proteins. In vivo, LB-100 and RT combined treatment prolonged the survival of mice with xenografts compared to RT alone. Taken together, these results provide convincing preclinical data to support the use of LB-100 as a radiosensitizing agent for treatment of malignant meningioma. Its potential for clinical application deserves further investigation.

Indexed as

Xenograft Model Antitumor AssaysAnimalsBridged Bicyclo Compounds, HeterocyclicCell Line, TumorCell SurvivalChemoradiotherapyDisease-Free SurvivalFemaleHumansMeningeal NeoplasmsMeningiomaMiceMice, Inbred BALB CMice, NudePiperazinesProtein Phosphatase 2Bridged Bicyclo Compounds, HeterocyclicLB100PiperazinesProtein Phosphatase 2LB-100MeningiomaPP2ARadiationSTAT3

Identifiers

PMID29199006
PMCPMC5748254
OpenAlexW2772173460

What OpenQuestion holds

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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.