Evidence map›Paper›PMID 29890668›Full record

ArticleMolecules (Basel, Switzerland)2018

Anti-Tumorigenic Activity of Chrysin from

Mai Nagasaka, Ryoko Hashimoto, Yasumichi Inoue, Kan'ichiro Ishiuchi, Michiyo Matsuno, Yuka Itoh, Muneshige Tokugawa, Nobumichi Ohoka, Daisuke Morishita, Hajime Mizukami and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Genome-Protecting Compounds as Potential Geroprotectors.International journal of molecular sciences · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Kurarinone fromMolecules (Basel, Switzerland) · 2019
    Article
  20. Ethnopharmacological Inspections of Organic Extract ofEvidence-based complementary and alternative medicine : eCAM · 2019
    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

12 authors at 3 institutions in 1 country.

Mai NagasakaDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. mercredi.le.mai@gmail.com.
Ryoko HashimotoDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. yr.12hh@gmail.com.
Yasumichi InoueDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. yukait@yamanashi.ac.jp.
Kan'ichiro IshiuchiDepartment of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University; Nagoya 467-8603, Japan. ishiuchi@phar.nagoya-cu.ac.jp.
Michiyo MatsunoThe Kochi Prefectural Makino Botanical Garden, Kochi 781-8125, Japan. matsuno@makino.or.jp.
Yuka ItohDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. yukait@yamanashi.ac.jp.
Muneshige TokugawaDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. shogun.fob@me.com.
Nobumichi OhokaDivision of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, Kawasaki 210-9501, Japan. n-ohoka@nihs.go.jp.
Daisuke MorishitaDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. daisuke.b.m.1215@gmail.com.
Hajime MizukamiThe Kochi Prefectural Makino Botanical Garden, Kochi 781-8125, Japan. hajimem@makino.or.jp.
Toshiaki MakinoDepartment of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University; Nagoya 467-8603, Japan. makino@phar.nagoya-cu.ac.jp.
Hidetoshi HayashiDepartment of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan. yainoue@phar.nagoya-cu.ac.jp.
Nagoya City University · JPMakino Botanical Garden · JPNational Institute of Health Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The p53 tumor suppressor plays critical roles in cell cycle regulation and apoptotic cell death in response to various cellular stresses, thereby preventing cancer development. Therefore, the activation of p53 through small molecules is an attractive therapeutic strategy for the treatment of cancers retaining wild-type p53. We used a library of 700 Myanmar wild plant extracts to identify small molecules that induce p53 transcriptional activity. A cell-based screening method with a p53-responsive luciferase-reporter assay system revealed that an ethanol extract of

Indexed as

Antineoplastic Agents, PhytogenicAtaxia Telangiectasia Mutated ProteinsBignoniaceaeCheckpoint Kinase 2DNA DamageFlavonoidsHumansMCF-7 CellsPlant ExtractsTranscription, GeneticTumor Suppressor Protein p53Antineoplastic Agents, PhytogenicAtaxia Telangiectasia Mutated ProteinsATM protein, humanCheckpoint Kinase 2CHEK2 protein, humanchrysinFlavonoidsPlant ExtractsTP53 protein, humanTumor Suppressor Protein p53ATMChk2chrysinflavonoidOroxylum indicump53

Identifiers

PMID29890668
PMCPMC6099937
OpenAlexW2805889788

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.