Evidence map›Paper›PMID 36358740›Full record

ReviewCancers2022

In Vivo Models for Prostate Cancer Research.

Robert Adamiecki, Anita Hryniewicz-Jankowska, Maria A Ortiz, Xiang Li, Baylee A Porter-Hansen, Imad Nsouli, Gennady Bratslavsky, Leszek Kotula

Abstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Key parameters for designing robust 2D and 3D spheroid models forBioengineering & translational medicine · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. 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.

Robert AdamieckiRutgers New Jersey Medical School, Rutgers University, Newark, NJ 07103, USA.ORCID 0000-0002-6701-9561
Anita Hryniewicz-JankowskaDepartment of Urology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.
Maria A OrtizDepartment of Urology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.ORCID 0000-0001-6785-5853
Xiang LiDepartment of Urology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.ORCID 0000-0002-5866-7866
Baylee A Porter-HansenDepartment of Urology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.
Imad NsouliDepartment of Biochemistry and Molecular Biology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.
Gennady BratslavskyDepartment of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, ul. F. Joliot-Curie 14a, 50-383 Wroclaw, Poland.ORCID 0000-0002-2712-4375
Leszek KotulaDepartment of Urology, SUNY Upstate Medical University, 750 East Adams Str., Syracuse, NY 13010, USA.ORCID 0000-0002-7977-7124

Funding

Sensitivity of Abi1/Pten null tumors to taxane and anti-androgen receptor therapyR21CA260381 · NCI · UPSTATE MEDICAL UNIVERSITY · PI KOTULA, LESZEK · 2021 to 2022
$413k
NCI NIH HHS R21 CA260381Upstate Medical University Pilot grant (Hendricks Fund) to LK N/A
6 · The paper itself

Abstract

In 2022, prostate cancer (PCa) is estimated to be the most commonly diagnosed cancer in men in the United States-almost 270,000 American men are estimated to be diagnosed with PCa in 2022. This review compares and contrasts in vivo models of PCa with regards to the altered genes, signaling pathways, and stages of tumor progression associated with each model. The main type of model included in this review are genetically engineered mouse models, which include conditional and constitutive knockout model. 2D cell lines, 3D organoids and spheroids, xenografts and allografts, and patient derived models are also included. The major applications, advantages and disadvantages, and ease of use and cost are unique to each type of model, but they all make it easier to translate the tumor progression that is seen in the mouse prostate to the human prostate. Although both human and mouse prostates are androgen-dependent, the fact that the native, genetically unaltered prostate in mice cannot give rise to carcinoma is an especially critical component of PCa models. Thanks to the similarities between the mouse and human genome, our knowledge of PCa has been expanded, and will continue to do so, through models of PCa.

Indexed as

genetically-engineered mouse modelsknockout mouse modelsorganoidspatient derived xenograftsprostate cancersignaling pathwaysxenografts

Identifiers

PMID36358740
PMCPMC9654339

What Socratic 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 Socratic graph.