Evidence map›Paper›PMID 31801263›Full record

ReviewMedical sciences (Basel, Switzerland)2019

Transient Receptor Potential Cation Channels in Cancer Therapy.

Giorgio Santoni, Federica Maggi, Maria Beatrice Morelli, Matteo Santoni, Oliviero Marinelli

Open access · goldAbstract readReview
In one paragraph

Review in Medical sciences (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.5field-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

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

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Roles of TRPM channels in glioma.Cancer biology & therapy · 2024
    Review
  7. Article
  8. Calcium and Neural Stem Cell Proliferation.International journal of molecular sciences · 2024
    Review
  9. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
    Review
  10. Role of TRP Channels in Metabolism-Related Diseases.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Review
  13. Identification of two novel autism genes,Frontiers in psychiatry · 2023
    Article
  14. Article
  15. Review
  16. Article
  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

5 authors at 2 institutions in 1 country.

Giorgio SantoniSchool of Pharmacy, University of Camerino, via Madonna delle Carceri 9, 62032 Camerino (MC), Italy.
Federica MaggiSchool of Pharmacy, University of Camerino, via Madonna delle Carceri 9, 62032 Camerino (MC), Italy.
Maria Beatrice MorelliSchool of Pharmacy, University of Camerino, via Madonna delle Carceri 9, 62032 Camerino (MC), Italy.
Matteo SantoniMedical Oncology Unit, Hospital of Macerata, Via Santa Lucia 2, 62100 Macerata (MC), Italy.
Oliviero MarinelliSchool of Pharmacy, University of Camerino, via Madonna delle Carceri 9, 62032 Camerino (MC), Italy.
Università di Camerino · ITUniversity of Macerata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In mammals, the transient receptor potential (TRP) channels family consists of six different families, namely TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPML (mucolipin), TRPP (polycystin), and TRPA (ankyrin), that are strictly connected with cancer cell proliferation, differentiation, cell death, angiogenesis, migration, and invasion. Changes in TRP channels' expression and function have been found to regulate cell proliferation and resistance or sensitivity of cancer cells to apoptotic-induced cell death, resulting in cancer-promoting effects or resistance to chemotherapy treatments. This review summarizes the data reported so far on the effect of targeting TRP channels in different types of cancer by using multiple TRP-specific agonists, antagonists alone, or in combination with classic chemotherapeutic agents, microRNA specifically targeting the TRP channels, and so forth, and the in vitro and in vivo feasibility evaluated in experimental models and in cancer patients. Considerable efforts have been made to fight cancer cells, and therapies targeting TRP channels seem to be the most promising strategy. However, more in-depth investigations are required to completely understand the role of TRP channels in cancer in order to design new, more specific, and valuable pharmacological tools.

Indexed as

chemotherapy resistancetransient receptor potential channelstumor progression

Identifiers

PMID31801263
PMCPMC6950741
OpenAlexW2990510102

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.