Evidence map›Paper›PMID 40976930›Full record

ReviewPigment cell & melanoma research2025

The Roles of PTEN in Melanoma Suppression.

Gennie L Parkman, Xiaonan Xu, Sheri L Holmen, Florian A Karreth

Abstract readReview
In one paragraph

Review in Pigment cell & melanoma research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. The Roles of PTEN in Melanoma Suppression.Pigment cell & melanoma research · 2025
    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

4 authors.

Gennie L ParkmanDepartment of Zoology, Weber State University, Ogden, Utah, USA.
Xiaonan XuDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, USA.
Sheri L HolmenHuntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City, Utah, USA.
Florian A KarrethDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, USA.

Funding

Efficacy of combined inhibition of BRAF, MEK, and FAK in melanoma patient derived xenograftsR01CA121118 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Sheri L Holmen · 2007 to 2026
$4.7M
Chromosome 1q ceRNAs in Melanoma Progression and MetastasisR01CA259046 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI KARRETH, FLORIAN · 2021 to 2025
$2.3M
Exploring miR-29 in melanoma progression and preventionR21CA256141 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI KARRETH, FLORIAN · 2021 to 2022
$419k
Congressionally Directed Medical Research Programs HT9425-23-1-0513Congressionally Directed Medical Research Programs HT9425-24-1-0402Melanoma Research Foundation 1068914NCI NIH HHS R01 CA121118NCI NIH HHS R01CA121118NCI NIH HHS R01 CA259046NCI NIH HHS R01CA259046NCI NIH HHS R21 CA256141NCI NIH HHS R21CA256141
6 · The paper itself

Abstract

Since its discovery more than a quarter century ago, PTEN has emerged as one of the most potent tumor suppressors and its loss of function is common to numerous cancer types including glioblastoma, prostate cancer, small cell lung cancer, and melanoma. PTEN is a lipid and protein phosphatase that contributes to various cellular processes, primarily by regulating key signaling pathways. Extensive research over the past two decades has uncovered many aspects of PTEN regulation and function and highlighted the role of PTEN in tumor suppression. PTEN loss-of-function is associated with the progression of a substantial portion of melanoma cases, and while its role in melanoma suppression is often ascribed to its inhibition of the PI3K/AKT signaling pathway, recent studies may hint at a more complex role for PTEN in melanoma. In this review, we provide an overview of how PTEN suppresses melanomagenesis.

Indexed as

MelanomaPTEN PhosphohydrolaseAnimalsHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanlipid phosphatasemelanomaprotein phosphatasePTENtumor suppressor

Identifiers

PMID40976930
PMCPMC12451098

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.