Evidence map›Paper›PMID 35205640›Full record

ReviewCancers2022

Precision Targets for Intercepting the Lethal Progression of Prostate Cancer: Potential Avenues for Personalized Therapy.

Max Christenson, Chung-Seog Song, Ya-Guang Liu, Bandana Chatterjee

Open access · goldAbstract 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
1.7field-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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Molecular insights for the tumor suppressor role of SPOP in prostate cancer.Biochimica et biophysica acta. Reviews on cancer · 2026
    Review
  3. Article
  4. Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    Article
  5. Review
  6. 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

4 authors at 1 institution in 1 country.

Max ChristensonDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA.
Chung-Seog SongDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA.
Ya-Guang LiuDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA.
Bandana ChatterjeeDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0003-1678-8659
The University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
AGING AND ANDROGEN RECEPTOR GENE REGULATIONR01AG010486 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHATTERJEE, BANDANA · 1993 to 2007
$1.1M
Aging and Prostatic Hyperplasia in Transgenic MiceR01AG019660 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI CHATTERJEE, BANDANA · 2002 to 2005
$1.0M
BLRD VA I01 BX000280NCI NIH HHS P30 CA054174NIA NIH HHS R01 AG010486NIA NIH HHS R01 AG019660US Department of Defense (DoD) and US Department of Veterans Affairs (VA) W81XWH-21-1-0307 (DoD); W81XWH-14-1-0606 (DoD); IK6 BX004207 (VA)
6 · The paper itself

Abstract

Organ-confined prostate cancer of low-grade histopathology is managed with radiation, surgery, active surveillance, or watchful waiting and exhibits a 5-year overall survival (OS) of 95%, while metastatic prostate cancer (PCa) is incurable, holding a 5-year OS of 30%. Treatment options for advanced PCa-metastatic and non-metastatic-include hormone therapy that inactivates androgen receptor (AR) signaling, chemotherapy and genome-targeted therapy entailing synthetic lethality of tumor cells exhibiting aberrant DNA damage response, and immune checkpoint inhibition (ICI), which suppresses tumors with genomic microsatellite instability and/or deficient mismatch repair. Cancer genome sequencing uncovered novel somatic and germline mutations, while mechanistic studies are revealing their pathological consequences. A microRNA has shown biomarker potential for stratifying patients who may benefit from angiogenesis inhibition prior to ICI. A 22-gene expression signature may select high-risk localized PCa, which would not additionally benefit from post-radiation hormone therapy. We present an up-to-date review of the molecular and therapeutic aspects of PCa, highlight genomic alterations leading to

Indexed as

androgen receptor axiscancer genomecastration resistancehigh-risk prostate cancerimmunotherapyneuroendocrine carcinomaPARP inhibitionprecision targeting

Identifiers

PMID35205640
PMCPMC8870390
OpenAlexW4213062434

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.