Evidence map›Paper›PMID 26657058›Full record

ReviewActa pharmacologica Sinica2016

Transient receptor potential channel C5 in cancer chemoresistance.

Dong-xu He, Xin Ma

Open access · bronzeAbstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Distribution of TRPC5 in the human lung: A study in body donors.Experimental and therapeutic medicine · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. KScientific reports · 2021
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Endothelial CaInternational journal of molecular sciences · 2018
    Review
  18. Ion channels research in the post-genomic era.Acta pharmacologica Sinica · 2016
    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

2 authors at 1 institution in 1 country.

Dong-xu HeNational Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi 214122, China.
Xin MaDepartment of Cellular and Molecular Pharmacology, School of Medicine and Pharmaceutics, Jiangnan University, Wuxi 214122, China.
Jiangnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential (TRP) superfamily contains at least 28 homologs in mammalian. These proteins form TRP channels are permeable to monovalent and divalent cations and participate in a variety of physiological functions. Dysregulation of TRP channels is responsible for numerous diseases. This review provides a brief short overview of mammalian TRP channels with a focus on TRPC5 and its role in cancers. Dysregulation of TRPC5 interrupts Ca(2+) homeostasis in cancer cells, which activates signaling pathways that are highly associated with cancer progression, especially cancer chemoresistance. Based on the important role of TRPC5, we also discuss the potential of TRPC5 as a target for therapeutic intervention. Either direct targeting of TRPC5 or indirect interruption of TRPC5-related signaling pathways may effectively overcome cancer chemoresistance.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic AgentsCalciumHomeostasisHumansMolecular Targeted TherapyMutationNeoplasmsSignal TransductionTRPC Cation ChannelsAntineoplastic AgentsCalciumTRPC5 protein, humanTRPC Cation Channels

Identifiers

PMID26657058
PMCPMC4722981
OpenAlexW2221165960

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.