Evidence map›Paper›PMID 36515844›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Examining the Effect of PARP-1 Inhibitors on Transcriptional Activity of Androgen Receptor in Prostate Cancer Cells.

Peter Makhov, Rushaniya Fazliyeva, Antonio Tufano, Robert G Uzzo, Vladimir M Kolenko

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 3% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. 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

5 authors at 2 institutions in 2 countries.

Peter MakhovMolecular Therapeutics Program, Fox Chase Cancer Center, Philadelphia, PA, USA.
Rushaniya FazliyevaCancer Signaling and Epigenetics Program, Fox Chase Cancer Center, Philadelphia, PA, USA.
Antonio TufanoUrology Unit, Department of Maternal-Child and Urological Sciences, "Sapienza" University of Rome, Rome, Italy.
Robert G UzzoDepartment of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.
Vladimir M KolenkoCancer Signaling and Epigenetics Program, Fox Chase Cancer Center, Philadelphia, PA, USA. Vladimir.Kolenko@fccc.edu.
Fox Chase Cancer Center · USSapienza University of Rome · IT

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Tumor-specific anti-angiogenic anti-CD70-FGF/VEGF-trap fusion antibodies for renal cancer therapyR21CA263362 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI MAKHOV, PETR B. · 2022 to 2023
$478k
The role of cholesterol homeostasis in enzalutamide resistanceR03CA235060 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI KOLENKO, VLADIMIR M · 2020 to 2021
$187k
Novel anti-CD70-VEGF-trap fusion antibodies as a next-generation therapeutic approach for renal cancerR03CA246011 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI MAKHOV, PETR B. · 2020 to 2021
$187k
Disrupting lysosomal sequestration of sunitinib by farnesyl-transferase inhibitors as a next generation therapeutic approach for TKI resistant RCCR03CA216173 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI MAKHOV, PETR B. · 2018 to 2019
$183k
NCI NIH HHS P30 CA006927NCI NIH HHS R03 CA216173NCI NIH HHS R03 CA235060NCI NIH HHS R03 CA246011NCI NIH HHS R21 CA263362
6 · The paper itself

Abstract

Since the early 1940s, androgen ablation has been the cornerstone of treatment for prostate cancer (PC). Importantly, androgen receptor (AR) signaling is vital not only for the initiation of PC, which is initially androgen-dependent, but also for castration-resistant disease. Recent studies demonstrated clear promise of the poly(ADP-ribose) polymerase 1 (PARP-1) inhibitors for targeting prostate cancer cells harboring mutations in DNA damage-repair genes. In addition, it has been established that PARP-1 inhibition suppresses growth of AR-positive prostate cancer cells in cell and animal models. Thus, prostate cancer represents a particularly promising disease site for targeting PARP-1, given that both DNA repair and AR-mediated transcription depend on PARP-1 function. Here, we describe the development and use of cell-based assay to evaluate the impact of PARP-1 inhibitors on the AR signaling in prostate cancer cells.

Indexed as

Poly(ADP-ribose) Polymerase InhibitorsProstatic NeoplasmsAndrogensAnimalsHumansMaleProstateReceptors, AndrogenAndrogensPoly(ADP-ribose) Polymerase InhibitorsReceptors, AndrogenAndrogen receptorCancerPARP-1Prostate

Identifiers

PMID36515844
PMCPMC10103651
OpenAlexW4311396924

What OpenQuestion holds

Textmetadata
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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.