Evidence map›Paper›PMID 30118500›Full record

ArticlePloS one2018

Trans-chalcone increases p53 activity via DNAJB1/HSP40 induction and CRM1 inhibition.

Gabriel Silva, Mozart Marins, Nadda Chaichanasak, Yongdae Yoon, Ana Lúcia Fachin, Vitor Caressato Pinhanelli, Luis Octávio Regasini, Mariana Bastos Dos Santos, Gabriela Miranda Ayusso, Beatriz de Carvalho Marques and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.2field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Chalcones and Gastrointestinal Cancers: Experimental Evidence.International journal of molecular sciences · 2023
    Review
  8. Review
  9. TheFrontiers in molecular biosciences · 2023
    Review
  10. Review
  11. Toxicological research · 2021
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Expression of exportin-1 in diffuse large B-cell lymphoma: immunohistochemistry and TCGA analyses.International journal of clinical and experimental pathology · 2018
    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 3 institutions in 2 countries.

Gabriel SilvaBiotechnology Unit, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Mozart MarinsBiotechnology Unit, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Nadda ChaichanasakLaboratory of Signal Transduction, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, Republic of Korea.
Yongdae YoonLaboratory of Signal Transduction, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, Republic of Korea.
Ana Lúcia FachinBiotechnology Unit, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Vitor Caressato PinhanelliBiotechnology Unit, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Luis Octávio RegasiniDepartment of Chemistry and Environmental Chemistry, São Paulo State University (UNESP), São Paulo, Brazil.
Mariana Bastos Dos SantosDepartment of Chemistry and Environmental Chemistry, São Paulo State University (UNESP), São Paulo, Brazil.
Gabriela Miranda AyussoDepartment of Chemistry and Environmental Chemistry, São Paulo State University (UNESP), São Paulo, Brazil.
Beatriz de Carvalho MarquesDepartment of Chemistry and Environmental Chemistry, São Paulo State University (UNESP), São Paulo, Brazil.
Wells W WuFacility for Biotechnology Resources, CBER, Food and Drug Administration, Silver Spring, Maryland, United States of America.
Je-Nie PhueFacility for Biotechnology Resources, CBER, Food and Drug Administration, Silver Spring, Maryland, United States of America.
Rong-Fong ShenFacility for Biotechnology Resources, CBER, Food and Drug Administration, Silver Spring, Maryland, United States of America.
Seung Joon BaekLaboratory of Signal Transduction, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-7866-7778
Universidade de Ribeirão Preto · BRUniversidade Estadual Paulista (Unesp) · BRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naturally-occurring chalcones and synthetic chalcone analogues have been demonstrated to have many biological effects, including anti-inflammatory, anti-malarial, anti-fungal, and anti-oxidant/anti-cancerous activities. Compared to other chalcones, trans-chalcone exhibits superior inhibitory activity in cancer cell growth as shown via in vitro assays, and exerts anti-cancerous effects via the activation of the p53 tumor suppressor protein. Thus, characterization of the specific mechanisms, by which trans-chalcone activates p53, can aid development of new chemotherapeutic drugs that can be used individually or synergistically with other drugs. In this report, we found that trans-chalcone modulates many p53 target genes, HSP40 being the most induced gene in the RNA-Seq data using trans-chalcone-treated cells. CRM1 is also inhibited by trans-chalcone, resulting in the accumulation of p53 and other tumor suppressor proteins in the nucleus. Similar effects were seen using trans-chalcone derivatives. Overall, trans-chalcone could provide a strong foundation for the development of chalcone-based anti-cancer drugs.

Indexed as

Activating Transcription Factor 3Antineoplastic AgentsCaspase 3Caspase 7Cell Line, TumorCell NucleusChalconeExportin 1 ProteinGrowth Differentiation Factor 15HSP40 Heat-Shock ProteinsHumansKaryopherinsReceptors, Cytoplasmic and NuclearSignal TransductionTranscription, GeneticTumor Suppressor Protein p53Activating Transcription Factor 3Antineoplastic AgentsATF3 protein, humanCASP3 protein, humanCASP7 protein, humanCaspase 3Caspase 7ChalconeDNAJB1 protein, humanExportin 1 ProteinGDF15 protein, humanGrowth Differentiation Factor 15HSP40 Heat-Shock ProteinsKaryopherinsReceptors, Cytoplasmic and NuclearTumor Suppressor Protein p53

Identifiers

PMID30118500
PMCPMC6097677
OpenAlexW2886212364

What OpenQuestion holds

Textmetadata
LicenceCC0
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.