Evidence map›Paper›PMID 25897893›Full record

ReviewCancer biology & therapy2015

LB100, a small molecule inhibitor of PP2A with potent chemo- and radio-sensitizing potential.

Christopher S Hong, Winson Ho, Chao Zhang, Chunzhang Yang, J Bradley Elder, Zhengping Zhuang

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

80 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Targeting PP2A in cancer: an underrated option.Journal of experimental & clinical cancer research : CR · 2025
    Review
  11. Article
  12. Exploiting Synthetic Lethality of PRMT5 for Precision Treatment of MTAP-Deficient Glioblastoma.International journal of translational medicine (Basel, Switzerland) · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

20 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 3 institutions in 1 country.

Christopher S Honga The Ohio State University Wexner Medical Center ; Department of Neurological Surgery ; Columbus , OH USA.
Winson Ho
Chao Zhang
Chunzhang Yang
J Bradley Elder
Zhengping Zhuang
National Institute of Neurological Disorders and Stroke · USNational Institutes of Health · USThe Ohio State University Wexner Medical Center · US

Funding

Molecular Pathogenesis of NeoplasiaZIANS003052 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI HEISS, JOHN · 2009 to 2025
$20.7M
Intramural NIH HHS
6 · The paper itself

Abstract

Protein phosphatase 2A (PP2A) is a serine/threonine phosphatase that plays a significant role in mitotic progression and cellular responses to DNA damage. While traditionally viewed as a tumor suppressor, inhibition of PP2A has recently come to attention as a novel therapeutic means of driving senescent cancer cells into mitosis and promoting cell death via mitotic catastrophe. These findings have been corroborated in numerous studies utilizing naturally produced compounds that selectively inhibit PP2A. To overcome the known human toxicities associated with these compounds, a water-soluble small molecule inhibitor, LB100, was recently developed to competitively inhibit the PP2A protein. This review summarizes the pre-clinical studies to date that have demonstrated the anti-cancer activity of LB100 via its chemo- and radio-sensitizing properties. These studies demonstrate the tremendous therapeutic potential of LB100 in a variety of cancer types. The results of an ongoing phase 1 trial are eagerly anticipated.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBridged Bicyclo Compounds, HeterocyclicCell CycleDrug Evaluation, PreclinicalDrug Resistance, NeoplasmEnzyme InhibitorsHumansMitosisNeoplasmsOncogene ProteinsPiperazinesProtein Phosphatase 2Radiation-Sensitizing AgentsTumor Protein, Translationally-Controlled 1Antineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicEnzyme InhibitorsLB100Oncogene ProteinsPiperazinesProtein Phosphatase 2Radiation-Sensitizing AgentsTPT1 protein, humanTpt1 protein, mouseTumor Protein, Translationally-Controlled 1Tumor Suppressor ProteinsABC, ATP-binding cassette.APC, adenomatous polyposis coliARPP19, cyclic AMP-regulated phosphoprotein 19ATM, ataxia-telangiectasia mutatedcell cyclechemosensitizationCIP2A, cancerous inhibitor of PP2ACNTF, ciliary neurotrophic factorDISC, death-inducing signaling complexDVL, dishevelledENSA, α-endosulphineGBM, glioblastomaGFAP, glial fibrillary acidic proteinHCC, hepatocellular carcinomaHDACs, histone deacetylase complexesHIF-1a, hypoxia-inducible factor-1aHRR, homologous recombination repairMDM2, mouse double minute 2 homologmitotic catastropheMRI, magnetic resonance imagingNPC, nasopharyngeal carcinomaPlk1, polo-like kinase 1PP2A, protein phosphatase 2Aprotein phosphatase 2Aradiosensitizationreviewsmall molecule inhibitorTCTP, translationally-controlled tumor proteinTMZ, temozolomideTRAIL, TNF-related apoptosis-inducing ligandVEGF, vascular endothelial growth factor

Identifiers

PMID25897893
PMCPMC4623051
OpenAlexW1606775748

What OpenQuestion holds

Textmetadata
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.