Evidence map›Paper›PMID 22897572›Full record

ArticleExperimental dermatology2012

Role of TRPM in melanocytes and melanoma.

Huazhang Guo, John Andrew Carlson, Andrzej Slominski

Open access · bronzeAbstract read
In one paragraph

Article in Experimental dermatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. TRP Channels in Skin Cancer: Focus on Malignant Melanoma.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
  11. Roles of TRPM channels in glioma.Cancer biology & therapy · 2024
    Review
  12. Article
  13. Article
  14. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
    Review
  15. The odyssey of the TR(i)P journey to the cellular membrane.Frontiers in cell and developmental biology · 2024
    Review
  16. Article
  17. TRPM2 Channels: A Potential Therapeutic Target in Melanoma?International journal of molecular sciences · 2023
    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

3 authors at 3 institutions in 1 country.

Huazhang GuoDepartment of Pathology, Westchester Medical Center, New York Medical College, Valhalla, NY, USA.
John Andrew Carlson
Andrzej Slominski
Albany Medical Center Hospital · USUniversity of Tennessee Health Science Center · USWestchester Medical Center · US

Funding

Novel Biosynthetic Pathway for Secosteroids and the SkinR01AR052190 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI POSTLETHWAITE, ARNOLD E, SLOMINSKI, ANDRZEJ T · 2006 to 2013
$2.2M
Role of Exogenous Melatonin in Skin BiologyR01AR056666 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SLOMINSKI, ANDRZEJ T · 2011 to 2015
$1.6M
NIAMS NIH HHS 1R01AR056666-01A2NIAMS NIH HHS R01 AR052190NIAMS NIH HHS R01AR052190NIAMS NIH HHS R01 AR056666
6 · The paper itself

Abstract

Transient receptor potential (TRP) cation channel superfamily plays important roles in variety cellular processes including polymodal cellular sensing, cell adhesion, cell polarity, proliferation, differentiation and apoptosis. One of its subfamilies are TRPM channels. mRNA expression of its founding member, TRPM1 (melastatin), correlates with terminal melanocytic differentiation and loss of its expression has been identified as an important diagnostic and prognostic marker for primary cutaneous melanoma. Because TRPM1 gene codes two transcripts: TRPM1 channel protein in its exons and miR-211 in one of its introns, we propose a dual role for TRPM1 gene where the loss of TRPM1 channel protein is an excellent marker of melanoma aggressiveness, while the expression of miR-211 is linked to the tumor suppressor function of TRPM1. In addition, three other members of this subfamily, TRPM 2, 7 and 8 are implicated in the regulation of melanocytic behaviour. TRPM2 is capable of inducing melanoma apoptosis and necrosis. TRPM7 can be a protector and detoxifier in both melanocytes and melanoma cells. TRPM8 can mediate agonist-induced melanoma cell death. Therefore, we propose that TRPM1, TRPM2, TRPM7 and TRPM8 play crucial roles in melanocyte physiology and melanoma oncology and are excellent diagnostic markers and theraputic targets.

Indexed as

ApoptosisBiomarkers, TumorExonsHumansIntronsMelanocytesMelanomaMicroRNAsNecrosisNeoplasm InvasivenessNeoplasm MetastasisProtein Serine-Threonine KinasesRNA, MessengerTRPM Cation ChannelsBiomarkers, TumorMicroRNAsMIRN211 microRNA, humanProtein Serine-Threonine KinasesRNA, MessengerTRPM1 protein, humanTRPM2 protein, humanTRPM7 protein, humanTRPM8 protein, humanTRPM Cation Channels

Identifiers

PMID22897572
PMCPMC3422761
OpenAlexW2040008189

What OpenQuestion holds

Textmetadata
LicenceTDM
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.