Evidence map›Paper›PMID 37393347›Full record

ArticleCell death discovery2023

Transient receptor potential ankyrin 1 (TRPA1) mediates reactive oxygen species-induced Ca

Pawan Faris, Agnese Rumolo, Giorgia Pellavio, Matteo Tanzi, Mauro Vismara, Roberto Berra-Romani, Andrea Gerbino, Salvatore Corallo, Paolo Pedrazzoli, Umberto Laforenza and 2 more

Abstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Journal of inflammation research · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. The role of TRPA1 in lung cancer.Translational lung cancer research · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. CaBiomedicines · 2025
    Review
  16. Review
  17. Role of TRP Channels in Cancer-Induced Bone Pain.International journal of molecular sciences · 2025
    Review
  18. Article
  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

12 authors.

Pawan FarisDepartment of Biology and Biotechnology "Lazzaro Spallanzani", University of Pavia, via Forlanini 6, 27100, Pavia, Italy.
Agnese RumoloFoundation IRCCS Policlinico San Matteo, Laboratory of Immunology Transplantation, Piazzale Golgi 19, Pavia, Italy.
Giorgia PellavioDepartment of Molecular Medicine, University of Pavia, via Forlanini 6, 27100, Pavia, Italy.
Matteo TanziFoundation IRCCS Policlinico San Matteo, Laboratory of Immunology Transplantation, Piazzale Golgi 19, Pavia, Italy.
Mauro VismaraDepartment of Biology and Biotechnology "Lazzaro Spallanzani", University of Pavia, via Forlanini 6, 27100, Pavia, Italy.
Roberto Berra-RomaniDepartment of Biomedicine, School of Medicine, Benemérita Universidad Autónoma de Puebla, 13 Sur 2702 Colonia Volcanes, Puebla, 72410, Mexico.
Andrea GerbinoDepartment of Biosciences, Biotechnologies and Environment, University of Bari Aldo Moro, Via G. Amendola 165/A, 70125, Bari, Italy.
Salvatore CoralloMedical Oncology, Foundation IRCCS Policlinico San Matteo, Piazzale Golgi 19, 27100, Pavia, Italy.ORCID http://orcid.org/0000-0002-6672-0233
Paolo PedrazzoliMedical Oncology, Foundation IRCCS Policlinico San Matteo, Piazzale Golgi 19, 27100, Pavia, Italy.
Umberto LaforenzaDepartment of Molecular Medicine, University of Pavia, via Forlanini 6, 27100, Pavia, Italy.
Daniela Montagna *Foundation IRCCS Policlinico San Matteo, Laboratory of Immunology Transplantation, Piazzale Golgi 19, Pavia, Italy. d.montagna@smatteo.pv.it.
Francesco Moccia *Department of Biology and Biotechnology "Lazzaro Spallanzani", University of Pavia, via Forlanini 6, 27100, Pavia, Italy. francesco.moccia@unipv.it.ORCID http://orcid.org/0000-0003-0010-0098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal carcinoma (CRC) represents the fourth most common cancer worldwide and is the third most common cause of malignancy-associated mortality. Distant metastases to the liver and lungs are the main drivers of CRC-dependent death. Pro-oxidant therapies, which halt disease progression by exacerbating oxidative stress, represent an antitumour strategy that is currently exploited by chemotherapy and ionizing radiation. A more selective strategy to therapeutically exploit reactive oxygen species (ROS) signaling would consist in targeting a redox sensor that is up-regulated in metastatic cells and is tightly coupled to the stimulation of cancer cell death programs. The non-selective cation channel, Transient Receptor Potential Ankyrin 1 (TRPA1), serves as a sensor of the cellular redox state, being activated to promote extracellular Ca

Identifiers

PMID37393347
PMCPMC10314907

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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.