Evidence map›Paper›PMID 37435458›Full record

ReviewEndocrine oncology (Bristol, England)2022

Regulatory genes in the androgen production, uptake and conversion (APUC) pathway in advanced prostate cancer.

Sean McSweeney, Hannah E Bergom, Anna Prizment, Susan Halabi, Nima Sharifi, Charles Ryan, Justin Hwang

Open access · diamondAbstract readReview
In one paragraph

Review in Endocrine oncology (Bristol, England), 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
0.9field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Prostate Cancer and the Mevalonate Pathway.International journal of molecular sciences · 2024
    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

7 authors at 4 institutions in 1 country.

Sean McSweeneyUniversity of Minnesota Medical School, Minneapolis, Minnesota, USA.ORCID 0000-0002-7682-2073
Hannah E BergomDepartment of Medicine, University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, USA.
Anna PrizmentDepartment of Medicine, University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, USA.
Susan HalabiDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Nima SharifiGenitourinary Malignancies Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0003-1281-3474
Charles RyanUniversity of Minnesota Medical School, Minneapolis, Minnesota, USA.
Justin HwangDepartment of Medicine, University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, USA.ORCID 0000-0003-1686-7103
University of Minnesota · USCleveland Clinic Lerner College of Medicine · USDuke University · USUniversity of Minnesota Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The androgen receptor (AR) signaling pathway regulates the progression of prostate cancer (PC). Metastatic castration-resistant prostate cancer (mCRPC) patients generally receive AR-targeted therapies (ART) or androgen-deprivation therapies (ADT) with the initial response; however, resistance is inevitably observed. Prior studies have shown activity and upregulation of a family of androgen production, uptake, and conversion - APUC genes - based on genomic analyses of patient germlines. Genetic variants of some APUC genes, such as the conversion gene, HSD3B1, predict response to second-generation androgen-targeted therapies. Studies have begun to elucidate the overall role of APUC genes, each with unique actionable enzymatic activity, in mCRPC patient outcomes. The current role and knowledge of the genetic and genomic features of APUC genes in advanced prostate cancer and beyond are discussed in this review. These studies inform of how interpreting behavior of APUC genes through genomic tools will impact the treatment of advanced prostate cancer.

Indexed as

androgensgenomicsprostate cancer

Identifiers

PMID37435458
PMCPMC10259352
OpenAlexW4281824504

What OpenQuestion 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 OpenQuestion graph.