Evidence map›Paper›PMID 31383920›Full record

ArticleScientific reports2019

Identifying potential novel drugs against Helicobacter pylori by targeting the essential response regulator HsrA.

Andrés González, Sandra Salillas, Adrián Velázquez-Campoy, Vladimir Espinosa Angarica, María F Fillat, Javier Sancho, Ángel Lanas

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Antimicrobial and Synergistic Activity of Metformin AgainstThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
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  4. Review
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  7. Challenges and Prospects for Eradication ofPathogens (Basel, Switzerland) · 2025
    Review
  8. Review
  9. Article
  10. World journal of clinical oncology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Identification of novel drug targets forFrontiers in bioinformatics · 2024
    Article
  15. Frontiers in pharmacology · 2024
    Article
  16. Article
  17. Development of apigenin loaded gastroretentive microsponge for the targeting ofSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
  18. Review
  19. 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

7 authors at 3 institutions in 3 countries.

Andrés GonzálezAragon Institute for Health Research (IIS Aragón), San Juan Bosco 13, 50009, Zaragoza, Spain. andresglezrod@gmail.com.ORCID http://orcid.org/0000-0002-0531-0943
Sandra SalillasInstitute for Biocomputation and Physics of Complex Systems, Mariano Esquillor (Edif. I + D), 50018, Zaragoza, Spain.
Adrián Velázquez-CampoyInstitute for Biocomputation and Physics of Complex Systems, Mariano Esquillor (Edif. I + D), 50018, Zaragoza, Spain.
Vladimir Espinosa AngaricaCancer Science Institute, National University of Singapore, 14 Medical Drive, #12-01, 117599, Singapore, Singapore.
María F FillatInstitute for Biocomputation and Physics of Complex Systems, Mariano Esquillor (Edif. I + D), 50018, Zaragoza, Spain.
Javier SanchoAragon Institute for Health Research (IIS Aragón), San Juan Bosco 13, 50009, Zaragoza, Spain.ORCID http://orcid.org/0000-0002-2879-9200
Ángel LanasAragon Institute for Health Research (IIS Aragón), San Juan Bosco 13, 50009, Zaragoza, Spain.ORCID http://orcid.org/0000-0001-5932-2889
Universidad de Zaragoza · ESFundacion Agencia Aragonesa para la Investigacion y el Desarrollo · ESNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing antibiotic resistance evolved by Helicobacter pylori has alarmingly reduced the eradication rates of first-line therapies. To overcome the current circulating resistome, we selected a novel potential therapeutic target in order to identify new candidate drugs for treating H. pylori infection. We screened 1120 FDA-approved drugs for molecules that bind to the essential response regulator HsrA and potentially inhibit its biological function. Seven natural flavonoids were identified as HsrA binders. All of these compounds noticeably inhibited the in vitro DNA binding activity of HsrA, but only four of them, apigenin, chrysin, kaempferol and hesperetin, exhibited high bactericidal activities against H. pylori. Chrysin showed the most potent bactericidal activity and the most synergistic effect in combination with clarithromycin or metronidazole. Flavonoid binding to HsrA occurs preferably at its C-terminal effector domain, interacting with amino acid residues specifically involved in forming the helix-turn-helix DNA binding motif. Our results validate the use of HsrA as a novel and effective therapeutic target in H. pylori infection and provide molecular evidence of a novel antibacterial mechanism of some natural flavonoids against H. pylori. The results further support the valuable potential of natural flavonoids as candidate drugs for novel antibacterial strategies.

Indexed as

Anti-Bacterial AgentsBacterial ProteinsDrug DiscoveryFlavonoidsHelicobacter InfectionsHelicobacter pyloriHumansMolecular Docking SimulationAnti-Bacterial AgentsBacterial ProteinsFlavonoids

Identifiers

PMID31383920
PMCPMC6683298
OpenAlexW2964441572

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.