Evidence map›Paper›PMID 30825185›Full record

ArticleBritish journal of pharmacology2019

Small molecule-facilitated anion transporters in cells for a novel therapeutic approach to cystic fibrosis.

Michele Fiore, Claudia Cossu, Valeria Capurro, Cristiana Picco, Alessandra Ludovico, Marcin Mielczarek, Israel Carreira-Barral, Emanuela Caci, Debora Baroni, Roberto Quesada and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2019. 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
3.7field-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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Lipophilic mono-guanidinesRSC advances · 2026
    Article
  3. Chlorination-Enhanced HChemistry, an Asian journal · 2026
    Article
  4. Review
  5. Article
  6. Anti-Microorganisms · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Recent Advances in Bioactive Artificial Ionophores.Chembiochem : a European journal of chemical biology · 2021
    Review
  12. Review
  13. New Therapies to Correct the Cystic Fibrosis Basic Defect.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

11 authors at 3 institutions in 2 countries.

Michele FioreIstituto di Biofisica, CNR, Genova, Italy.
Claudia CossuIstituto di Biofisica, CNR, Genova, Italy.
Valeria CapurroU.O.C. Genetica Medica, Istituto Giannina Gaslini, Genova, Italy.
Cristiana PiccoIstituto di Biofisica, CNR, Genova, Italy.
Alessandra LudovicoIstituto di Biofisica, CNR, Genova, Italy.
Marcin MielczarekDepartamento de Química, Facultad de Ciencias, Universidad de Burgos, Burgos, Spain.
Israel Carreira-BarralDepartamento de Química, Facultad de Ciencias, Universidad de Burgos, Burgos, Spain.
Emanuela CaciU.O.C. Genetica Medica, Istituto Giannina Gaslini, Genova, Italy.
Debora BaroniIstituto di Biofisica, CNR, Genova, Italy.
Roberto QuesadaDepartamento de Química, Facultad de Ciencias, Universidad de Burgos, Burgos, Spain.
Oscar MoranIstituto di Biofisica, CNR, Genova, Italy.ORCID 0000-0003-1287-6176
Instituto di Biofisica · ESUniversidad de Burgos · ESIstituto Giannina Gaslini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeCystic fibrosis (CF) is a lethal autosomal recessive genetic disease that originates from the defective function of the CF transmembrane conductance regulator (CFTR) protein, a cAMP-dependent anion channel involved in fluid transport across epithelium. Because small synthetic transmembrane anion transporters (anionophores) can replace the biological anion transport mechanisms, independent of genetic mutations in the CFTR, such anionophores are candidates as new potential treatments for CF. EXPERIMENTAL APPROACH: In order to assess their effects on cell physiology, we have analysed the transport properties of five anionophore compounds, three prodigiosines and two tambjamines. Chloride efflux was measured in large uni-lamellar vesicles and in HEK293 cells with chloride-sensitive electrodes. Iodide influx was evaluated in FRT cells transfected with iodide-sensitive YFP. Transport of bicarbonate was assessed by changes of pH after a NH KEY

resultsAll studied compounds are capable of transporting halides and bicarbonate across the cell membrane, with a higher transport capacity at acidic pH. Interestingly, the presence of these anionophores did not interfere with the activation of CFTR and did not modify the action of lumacaftor (a CFTR corrector) or ivacaftor (a CFTR potentiator). CONCLUSION AND IMPLICATIONS: These anionophores, at low concentrations, transported chloride and bicarbonate across cell membranes, without affecting CFTR function. They therefore provide promising starting points for the development of novel treatments for CF.

Indexed as

AnimalsBicarbonatesCell LineCell SurvivalChloridesCricetulusCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDrug InteractionsHumansHydrogen-Ion ConcentrationIodidesIonophoresIon TransportMembrane PotentialsRatsBicarbonatesChloridesCystic Fibrosis Transmembrane Conductance RegulatorIodidesIonophores

Identifiers

PMID30825185
PMCPMC6514296
OpenAlexW2920074298

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.