Evidence map›Paper›PMID 35053150›Full record

ReviewBiomolecules2021

TRP Channels as Molecular Targets to Relieve Cancer Pain.

Milena Duitama, Yurany Moreno, Sandra Paola Santander, Zulma Casas, Jhon Jairo Sutachan, Yolima P Torres, Sonia L Albarracín

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Role of TRP Channels in Cancer-Induced Bone Pain.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. TRPA1, TRPV1, and Caffeine: Pain and Analgesia.International journal of molecular sciences · 2024
    Review
  17. Article
  18. Review
  19. Review
  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

7 authors at 3 institutions in 2 countries.

Milena DuitamaDepartamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Yurany MorenoDepartment of Lymphoma & Myeloma, MD Anderson Cancer Center, The University of Texas, Houston, TX 77030, USA.
Sandra Paola SantanderPhytoimmunomodulation Research Group, Juan N. Corpas University Foundation, Bogotá 111111, Colombia.
Zulma CasasDepartamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Jhon Jairo SutachanDepartamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Yolima P TorresDepartamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Sonia L AlbarracínDepartamento de Nutrición y Bioquímica, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Pontificia Universidad Javeriana · COFundación Universitaria Juan N. Corpas · COThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential (TRP) channels are critical receptors in the transduction of nociceptive stimuli. The microenvironment of diverse types of cancer releases substances, including growth factors, neurotransmitters, and inflammatory mediators, which modulate the activity of TRPs through the regulation of intracellular signaling pathways. The modulation of TRP channels is associated with the peripheral sensitization observed in patients with cancer, which results in mild noxious sensory stimuli being perceived as hyperalgesia and allodynia. Secondary metabolites derived from plant extracts can induce the activation, blocking, and desensitization of TRP channels. Thus, these compounds could act as potential therapeutic agents, as their antinociceptive properties could be beneficial in relieving cancer-derived pain. In this review, we will summarize the role of TRPV1 and TRPA1 in pain associated with cancer and discuss molecules that have been reported to modulate these channels, focusing particularly on the mechanisms of channel activation associated with molecules released in the tumor microenvironment.

Indexed as

Cancer PainNeoplasm ProteinsNeoplasmsSignal TransductionTRPA1 Cation ChannelTRPV Cation ChannelsAnimalsHumansHyperalgesiaNeoplasm ProteinsTRPA1 Cation ChannelTRPA1 protein, humanTRPV1 protein, humanTRPV Cation ChannelscancerpainTRP channels

Identifiers

PMID35053150
PMCPMC8774023
OpenAlexW4200612863

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.