Evidence map›Paper›PMID 30425290›Full record

ArticleScientific reports2018

The anti-tumor diterpene oridonin is a direct inhibitor of Nucleolin in cancer cells.

Michele Vasaturo, Roberta Cotugno, Lorenzo Fiengo, Claudio Vinegoni, Fabrizio Dal Piaz, Nunziatina De Tommasi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Oridonin fromFood science & nutrition · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Exploring the Anticancer Potential ofPlants (Basel, Switzerland) · 2023
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. RNA binding proteins in osteoarthritis.Frontiers in cell and developmental biology · 2022
    Review
  19. Article
  20. Review
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 2 institutions in 2 countries.

Michele VasaturoUniversità degli Studi di Salerno, Department of Pharmacy, Via Giovanni Paolo II, 84084, Fisciano, (SA), Italy.
Roberta CotugnoUniversità degli Studi di Salerno, Department of Pharmacy, Via Giovanni Paolo II, 84084, Fisciano, (SA), Italy.
Lorenzo FiengoUniversità degli Studi di Salerno, Department of Pharmacy, Via Giovanni Paolo II, 84084, Fisciano, (SA), Italy.
Claudio VinegoniHarvard Medical School, MGH Center for Systems Biology, 185 Cambridge Steet, 02144, Boston, MA, USA.
Fabrizio Dal PiazUniversità degli Studi di Salerno, Department of Medicine and Surgery, Via S. Allende, 84081, Baronissi, (SA), Italy. fdalpiaz@unisa.it.
Nunziatina De TommasiUniversità degli Studi di Salerno, Department of Pharmacy, Via Giovanni Paolo II, 84084, Fisciano, (SA), Italy.
University of Salerno · ITHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bioactive plant diterpene oridonin displays important pharmacological activities and is widely used in traditional Chinese medicine; however, its molecular mechanism of action is still incompletely described. In vitro and in vivo data have demonstrated anti-tumor activity of oridonin and its ability to interfere with several cell pathways; however, presently only the molecular chaperone HSP70 has been identified as a direct potential target of this compound. Here, using a combination of different proteomic approaches, innovative Cellular Thermal Shift Assay (CETSA) experiments, and classical biochemical methods, we demonstrate that oridonin interacts with Nucleolin, effectively modulating the activity of this multifunctional protein. The ability of oridonin to target Nucleolin and/or HSP70 could account for the bioactivity profile of this plant diterpene. Recently, Nucleolin has attracted attention as a druggable target, as its diverse functions are implicated in pathological processes such as cancer, inflammation, and viral infection. However, up to now, no small molecule as Nucleolin binders has been reported, thus our finding represents the first evidence of Nucleolin modulation by a small inhibitor.

Indexed as

Antineoplastic AgentsBiological TransportDiterpenes, KauraneHeLa CellsHumansJurkat CellsNucleolinPhosphoproteinsRNA-Binding ProteinsAntineoplastic AgentsDiterpenes, KauraneNucleolinoridoninPhosphoproteinsRNA-Binding Proteins

Identifiers

PMID30425290
PMCPMC6233161
OpenAlexW2900235537

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.