Evidence map›Paper›PMID 33376561›Full record

ReviewDisease markers2020

TRPV2: A Cancer Biomarker and Potential Therapeutic Target.

Kodappully S Siveen, Parveen B Nizamuddin, Shahab Uddin, Mohamed Al-Thani, Michael Paul Frenneaux, Ibrahim A Janahi, Martin Steinhoff, Fouad Azizi

Open access · hybridAbstract readReview
In one paragraph

Review in Disease markers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
3.1field-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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Cannabidiol-Ion Channel Interactions Represent a Promising Preventive and Therapeutic Strategy in Hepatocellular Carcinoma.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. TRPV4 Channel Modulators as Potential Drug Candidates for Cystic Fibrosis.International journal of molecular sciences · 2024
    Review
  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

8 authors at 3 institutions in 2 countries.

Kodappully S SiveenTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Parveen B NizamuddinTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Shahab UddinTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Mohamed Al-ThaniPublic Health Department, Ministry of Public Health, Doha, Qatar.
Michael Paul FrenneauxTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Ibrahim A JanahiDivision of Pediatric Pulmonology Sidra Medicine, Doha, Qatar.
Martin SteinhoffTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.
Fouad AziziTranslational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.ORCID https://orcid.org/0000-0001-7793-2250
Hamad Medical Corporation · QAMinistry of Public Health · QACornell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Transient Receptor Potential Vanilloid type-2 (TRPV2) channel exhibits oncogenicity in different types of cancers. TRPV2 is implicated in signaling pathways that mediate cell survival, proliferation, and metastasis. In leukemia and bladder cancer, the oncogenic activity of TRPV2 was linked to alteration of its expression profile. In multiple myeloma patients, TRPV2 overexpression correlated with bone tissue damage and poor prognosis. In prostate cancer, TRPV2 overexpression was associated with the castration-resistant phenotype and metastasis. Loss or inactivation of TRPV2 promoted glioblastoma cell proliferation and increased resistance to CD95-induced apoptotic cell death. TRPV2 overexpression was associated with high relapse-free survival in triple-negative breast cancer, whereas the opposite was found in patients with esophageal squamous cell carcinoma or gastric cancer. Another link was found between TRPV2 expression and either drug-induced cytotoxicity or stemness of liver cancer. Overall, these findings validate TRPV2 as a prime candidate for cancer biomarker and future therapeutic target.

Indexed as

Biomarkers, TumorFemaleHumansMaleMolecular Targeted TherapyNeoplasmsTRPV Cation ChannelsBiomarkers, TumorTRPV2 protein, humanTRPV Cation Channels

Identifiers

PMID33376561
PMCPMC7746447
OpenAlexW3111745362

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.