Evidence map›Paper›PMID 36882525›Full record

ArticleOncogene2023

TRIM28 promotes luminal cell plasticity in a mouse model of prostate cancer.

Ashutosh S Yende, Emily C Williams, Andrew Pletcher, Alexandra Helfand, Helen Ibeawuchi, Tanya M North, Patricia S Latham, Anelia Horvath, Maho Shibata

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Androgen Signaling in Prostate Cancer: When a Friend Turns Foe.Endocrine, metabolic & immune disorders drug targets · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. TRIM28 in cancer and cancer therapy.Frontiers in genetics · 2024
    Review
  10. 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

9 authors at 2 institutions in 1 country.

Ashutosh S Yende *Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Emily C Williams *Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.ORCID 0000-0002-5561-6553
Andrew PletcherDepartment of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Alexandra HelfandDepartment of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Helen IbeawuchiDepartment of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Tanya M NorthDepartment of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.ORCID 0000-0001-6184-8943
Patricia S LathamThe George Washington University Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.ORCID 0000-0003-2782-9444
Anelia HorvathThe George Washington University Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Maho ShibataDepartment of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA. mshibata@gwu.edu.ORCID 0000-0002-7056-3939
George Washington University · USJohns Hopkins University · US

Funding

Investigation of luminal stem cells and castration resistance in prostate cancerR00CA194287 · NCI · GEORGE WASHINGTON UNIVERSITY · PI SHIBATA, MAHO · 2018 to 2020
$740k
NCI NIH HHS R00 CA194287
6 · The paper itself

Abstract

The Tripartite motif-containing 28 (TRIM28) transcriptional cofactor is significantly upregulated in high-grade and metastatic prostate cancers. To study the role of TRIM28 in prostate cancer progression in vivo, we generated a genetically-engineered mouse model, combining prostate-specific inactivation of Trp53, Pten and Trim28. Trim28 inactivated NPp53T mice developed an inflammatory response and necrosis in prostate lumens. By conducting single-cell RNA sequencing, we found that NPp53T prostates had fewer luminal cells resembling proximal luminal lineage cells, which are cells with progenitor activity enriched in proximal prostates and prostate invagination tips in wild-type mice with analogous populations in human prostates. However, despite increased apoptosis and reduction of cells expressing proximal luminal cell markers, we found that NPp53T mouse prostates evolved and progressed to invasive prostate carcinoma with a shortened overall survival. Altogether, our findings suggest that TRIM28 promotes expression of proximal luminal cell markers in prostate tumor cells and provides insights into TRIM28 function in prostate tumor plasticity.

Indexed as

Cell PlasticityProstatic NeoplasmsAnimalsDisease Models, AnimalHumansMaleMiceNeoplastic Stem CellsProstateTripartite Motif-Containing Protein 28TRIM28 protein, humanTrim28 protein, mouseTripartite Motif-Containing Protein 28

Identifiers

PMID36882525
PMCPMC10122711
OpenAlexW4323349376

What Socratic 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 Socratic graph.