Evidence map›Paper›PMID 35049094›Full record

ArticleMolecular carcinogenesis2022

Stage-specific differential expression of zinc transporter SLC30A and SLC39A family proteins during prostate tumorigenesis.

Ram R Prasad, Komal Raina, Neha Mishra, Munendra S Tomar, Robin Kumar, Amy E Palmer, Paul Maroni, Rajesh Agarwal

Abstract read
In one paragraph

Article in Molecular carcinogenesis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
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  4. Metal-related cell death and its application in pancreatic cancer.Expert reviews in molecular medicine · 2025
    Review
  5. Article
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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 4 institutions in 1 country.

Ram R PrasadDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Komal RainaDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Neha MishraDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Munendra S TomarDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Robin KumarDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, South Dakota, USA.
Amy E PalmerDepartment of Biochemistry, BioFrontiers Institute, University of Colorado, Boulder, Colorado, USA.
Paul MaroniDepartment of Surgery, Division of Urology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Rajesh AgarwalDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.ORCID 0000-0002-9455-0235
University of Colorado Anschutz Medical Campus · USSouth Dakota State University · USUniversity of Colorado Boulder · USUniversity of Colorado Cancer Center · US

Funding

lluminating the biochemistry of zinc and RNA in live cellsR35GM139644 · NIGMS · UNIVERSITY OF COLORADO · PI Amy E Palmer · 2021 to 2026
$3.7M
NIGMS NIH HHS R35 GM139644
6 · The paper itself

Abstract

Prostate cancer (PCa) initiation and progression uniquely modify the prostate milieu to aid unrestrained cell proliferation. One salient modification is the loss of the ability of prostate epithelial cells to accumulate high concentrations of zinc; however, molecular alterations associated with loss of zinc accumulating capability in malignant prostate cells remain poorly understood. Herein, we assessed the stage-specific expression of zinc transporters (ZNTs) belonging to the ZNT (SLC30A) and Zrt- and Irt-like protein (ZIP) (SLC39A) solute-carrier family in the prostate tissues of different genetically engineered mouse models (GEMM) of PCa (TMPRSS2-ERG.Pten

Indexed as

AdenocarcinomaCation Transport ProteinsProstatic NeoplasmsCarcinogenesisCarrier ProteinsCell Transformation, NeoplasticHumansMaleProstateZincCarrier ProteinsCation Transport ProteinsZinczinc-binding proteinHi-Myc+/−human tissuesprostate cancerSLC30ASLC39ATMPRSS2-ERG.Ptenflox/floxTRAMPzinc transporters

Identifiers

PMID35049094
PMCPMC11952371
OpenAlexW4206752112

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.